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{
"count": 220212,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2203",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2201",
"results": [
{
"created": "2019-11-17T16:13:59.442157+11:00",
"panel_name": "Early-onset Dementia_MGHA_VCGS",
"panel_id": 24,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Early-onset Dementia_MGHA_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:12:33.619218+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBGCP4 was added\ngene: TUBGCP4 was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBGCP4 was set to Unknown",
"entity_name": "TUBGCP4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.550995+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBG1 was added\ngene: TUBG1 was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBG1 was set to Unknown",
"entity_name": "TUBG1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.481675+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB3 was added\ngene: TUBB3 was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB3 was set to Unknown",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.414181+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB2B was added\ngene: TUBB2B was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB2B was set to Unknown",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.346475+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB2A was added\ngene: TUBB2A was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB2A was set to Unknown",
"entity_name": "TUBB2A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.277530+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB was added\ngene: TUBB was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB was set to Unknown",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.209114+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA8 was added\ngene: TUBA8 was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBA8 was set to Unknown",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.140552+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA1A was added\ngene: TUBA1A was added to Tubulinopathies_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBA1A was set to Unknown",
"entity_name": "TUBA1A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:33.096348+11:00",
"panel_name": "Tubulinopathies_AustralianGenomics_VCGS",
"panel_id": 21,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Tubulinopathies_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:12:20.116438+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TSC2 was added\ngene: TSC2 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TSC2 was set to Unknown",
"entity_name": "TSC2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.978123+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TSC1 was added\ngene: TSC1 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TSC1 was set to Unknown",
"entity_name": "TSC1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.908761+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STRADA was added\ngene: STRADA was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: STRADA was set to Unknown",
"entity_name": "STRADA",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.841122+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PTEN was added\ngene: PTEN was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PTEN was set to Unknown",
"entity_name": "PTEN",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.772756+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NPRL3 was added\ngene: NPRL3 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NPRL3 was set to Unknown",
"entity_name": "NPRL3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.703950+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NPRL2 was added\ngene: NPRL2 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NPRL2 was set to Unknown",
"entity_name": "NPRL2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.636605+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MTOR was added\ngene: MTOR was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: MTOR was set to Unknown",
"entity_name": "MTOR",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.566077+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DEPDC5 was added\ngene: DEPDC5 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: DEPDC5 was set to Unknown",
"entity_name": "DEPDC5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.482125+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BRAF was added\ngene: BRAF was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: BRAF was set to Unknown",
"entity_name": "BRAF",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.413315+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AKT3 was added\ngene: AKT3 was added to Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: AKT3 was set to Unknown",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:19.368939+11:00",
"panel_name": "Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"panel_id": 20,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Tuberous sclerosis, cortical dysplasia and hemimegalencephaly_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:12:04.450447+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NEDD4L was added\ngene: NEDD4L was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: NEDD4L was set to Unknown",
"entity_name": "NEDD4L",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:04.371615+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MAP1B was added\ngene: MAP1B was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: MAP1B was set to Unknown",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:04.293035+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FLNA was added\ngene: FLNA was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: FLNA was set to Unknown",
"entity_name": "FLNA",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:04.215195+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FAT4 was added\ngene: FAT4 was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: FAT4 was set to Unknown",
"entity_name": "FAT4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:04.135995+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ERMARD was added\ngene: ERMARD was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: ERMARD was set to Unknown",
"entity_name": "ERMARD",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:04.057699+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DCHS1 was added\ngene: DCHS1 was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: DCHS1 was set to Unknown",
"entity_name": "DCHS1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:03.975245+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARFGEF2 was added\ngene: ARFGEF2 was added to Periventricular grey matter heterotopia_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Australian Genomics Health Alliance Brain Malformation Flagship\nMode of inheritance for gene: ARFGEF2 was set to Unknown",
"entity_name": "ARFGEF2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:12:03.926024+11:00",
"panel_name": "Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"panel_id": 19,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Periventricular grey matter heterotopia_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:11:37.676963+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: WDR62 was added\ngene: WDR62 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: WDR62 was set to Unknown",
"entity_name": "WDR62",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.604294+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB3 was added\ngene: TUBB3 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB3 was set to Unknown",
"entity_name": "TUBB3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.531707+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB2B was added\ngene: TUBB2B was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB2B was set to Unknown",
"entity_name": "TUBB2B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.458065+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBB was added\ngene: TUBB was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBB was set to Unknown",
"entity_name": "TUBB",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.385186+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA8 was added\ngene: TUBA8 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBA8 was set to Unknown",
"entity_name": "TUBA8",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.311002+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA1A was added\ngene: TUBA1A was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBA1A was set to Unknown",
"entity_name": "TUBA1A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.235746+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM216 was added\ngene: TMEM216 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TMEM216 was set to Unknown",
"entity_name": "TMEM216",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.161889+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SRPX2 was added\ngene: SRPX2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: SRPX2 was set to Unknown",
"entity_name": "SRPX2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.087220+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SIX3 was added\ngene: SIX3 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: SIX3 was set to Unknown",
"entity_name": "SIX3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:37.004352+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SHH was added\ngene: SHH was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: SHH was set to Unknown",
"entity_name": "SHH",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.930739+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RTTN was added\ngene: RTTN was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: RTTN was set to Unknown",
"entity_name": "RTTN",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.857398+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RAB3GAP2 was added\ngene: RAB3GAP2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: RAB3GAP2 was set to Unknown",
"entity_name": "RAB3GAP2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.784528+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RAB3GAP1 was added\ngene: RAB3GAP1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: RAB3GAP1 was set to Unknown",
"entity_name": "RAB3GAP1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.714603+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RAB18 was added\ngene: RAB18 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: RAB18 was set to Unknown",
"entity_name": "RAB18",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.642581+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIK3R2 was added\ngene: PIK3R2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PIK3R2 was set to Unknown",
"entity_name": "PIK3R2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.568902+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PIK3CA was added\ngene: PIK3CA was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PIK3CA was set to Unknown",
"entity_name": "PIK3CA",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.498117+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PI4KA was added\ngene: PI4KA was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PI4KA was set to Unknown",
"entity_name": "PI4KA",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.426554+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PAX6 was added\ngene: PAX6 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PAX6 was set to Unknown",
"entity_name": "PAX6",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.353659+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: OCLN was added\ngene: OCLN was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: OCLN was set to Unknown",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.280569+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NSDHL was added\ngene: NSDHL was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NSDHL was set to Unknown",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.208457+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NHEJ1 was added\ngene: NHEJ1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NHEJ1 was set to Unknown",
"entity_name": "NHEJ1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:36.100530+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NDE1 was added\ngene: NDE1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NDE1 was set to Unknown",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.955607+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: MAP1B was added\ngene: MAP1B was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: MAP1B was set to Unknown",
"entity_name": "MAP1B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.884925+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LAMC3 was added\ngene: LAMC3 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LAMC3 was set to Unknown",
"entity_name": "LAMC3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.814191+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: L1CAM was added\ngene: L1CAM was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: L1CAM was set to Unknown",
"entity_name": "L1CAM",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.742476+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF5C was added\ngene: KIF5C was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KIF5C was set to Unknown",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.672530+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF1BP was added\ngene: KIF1BP was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KIF1BP was set to Unknown",
"entity_name": "KIF1BP",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.602210+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: INTS8 was added\ngene: INTS8 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: INTS8 was set to Unknown",
"entity_name": "INTS8",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.532253+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GRIN2B was added\ngene: GRIN2B was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: GRIN2B was set to Unknown",
"entity_name": "GRIN2B",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.461590+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GRIN1 was added\ngene: GRIN1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: GRIN1 was set to Unknown",
"entity_name": "GRIN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.391755+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FIG4 was added\ngene: FIG4 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: FIG4 was set to Unknown",
"entity_name": "FIG4",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.319027+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EOMES was added\ngene: EOMES was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: EOMES was set to Unknown",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.250210+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EMX2 was added\ngene: EMX2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: EMX2 was set to Unknown",
"entity_name": "EMX2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.181431+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EML1 was added\ngene: EML1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: EML1 was set to Unknown",
"entity_name": "EML1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.111918+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DYNC1H1 was added\ngene: DYNC1H1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: DYNC1H1 was set to Unknown",
"entity_name": "DYNC1H1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:35.007950+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL4A1 was added\ngene: COL4A1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: COL4A1 was set to Unknown",
"entity_name": "COL4A1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.939006+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: COL18A1 was added\ngene: COL18A1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: COL18A1 was set to Unknown",
"entity_name": "COL18A1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.869069+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: BICD2 was added\ngene: BICD2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: BICD2 was set to Unknown",
"entity_name": "BICD2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.800133+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ATP1A2 was added\ngene: ATP1A2 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ATP1A2 was set to Unknown",
"entity_name": "ATP1A2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.730213+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ASTN1 was added\ngene: ASTN1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ASTN1 was set to Unknown",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.662298+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARX was added\ngene: ARX was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ARX was set to Unknown",
"entity_name": "ARX",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.594629+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AKT3 was added\ngene: AKT3 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: AKT3 was set to Unknown",
"entity_name": "AKT3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.527117+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AHI1 was added\ngene: AHI1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: AHI1 was set to Unknown",
"entity_name": "AHI1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.436997+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADGRG1 was added\ngene: ADGRG1 was added to Polymicrogyria and schizencephaly_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ADGRG1 was set to Unknown",
"entity_name": "ADGRG1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:11:34.391084+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "panel",
"text": "Added panel Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"entity_name": null,
"entity_type": null
},
{
"created": "2019-11-17T16:10:46.020228+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: VLDLR was added\ngene: VLDLR was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: VLDLR was set to Unknown",
"entity_name": "VLDLR",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.948320+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TUBA1A was added\ngene: TUBA1A was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TUBA1A was set to Unknown",
"entity_name": "TUBA1A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.876963+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SRD5A3 was added\ngene: SRD5A3 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: SRD5A3 was set to Unknown",
"entity_name": "SRD5A3",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.804678+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SNAP29 was added\ngene: SNAP29 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: SNAP29 was set to Unknown",
"entity_name": "SNAP29",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.734219+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: TMEM5 was added\ngene: TMEM5 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: TMEM5 was set to Unknown",
"entity_name": "TMEM5",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.664268+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: RELN was added\ngene: RELN was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: RELN was set to Unknown",
"entity_name": "RELN",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.594197+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: PAFAH1B1 was added\ngene: PAFAH1B1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: PAFAH1B1 was set to Unknown",
"entity_name": "PAFAH1B1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.523851+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: NDE1 was added\ngene: NDE1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: NDE1 was set to Unknown",
"entity_name": "NDE1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.454498+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LARGE1 was added\ngene: LARGE1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LARGE1 was set to Unknown",
"entity_name": "LARGE1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.384263+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LAMB1 was added\ngene: LAMB1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LAMB1 was set to Unknown",
"entity_name": "LAMB1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.314150+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: LAMA2 was added\ngene: LAMA2 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: LAMA2 was set to Unknown",
"entity_name": "LAMA2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:45.244011+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF5C was added\ngene: KIF5C was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KIF5C was set to Unknown",
"entity_name": "KIF5C",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.986104+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: KIF2A was added\ngene: KIF2A was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: KIF2A was set to Unknown",
"entity_name": "KIF2A",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.915193+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ISPD was added\ngene: ISPD was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ISPD was set to Unknown",
"entity_name": "ISPD",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.846217+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: GMPPB was added\ngene: GMPPB was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: GMPPB was set to Unknown",
"entity_name": "GMPPB",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.777673+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: EML1 was added\ngene: EML1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: EML1 was set to Unknown",
"entity_name": "EML1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.708483+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DYNC1H1 was added\ngene: DYNC1H1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: DYNC1H1 was set to Unknown",
"entity_name": "DYNC1H1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.640141+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DCX was added\ngene: DCX was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: DCX was set to Unknown",
"entity_name": "DCX",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.571692+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CTNNA2 was added\ngene: CTNNA2 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: CTNNA2 was set to Unknown",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.502602+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CRADD was added\ngene: CRADD was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: CRADD was set to Unknown",
"entity_name": "CRADD",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.428557+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: B4GAT1 was added\ngene: B4GAT1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: B4GAT1 was set to Unknown",
"entity_name": "B4GAT1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.350212+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: B3GNT2 was added\ngene: B3GNT2 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: B3GNT2 was set to Unknown",
"entity_name": "B3GNT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.266061+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: B3GALNT2 was added\ngene: B3GALNT2 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: B3GALNT2 was set to Unknown",
"entity_name": "B3GALNT2",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.197505+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ARX was added\ngene: ARX was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ARX was set to Unknown",
"entity_name": "ARX",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.124914+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTG1 was added\ngene: ACTG1 was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ACTG1 was set to Unknown",
"entity_name": "ACTG1",
"entity_type": "gene"
},
{
"created": "2019-11-17T16:10:44.054293+11:00",
"panel_name": "Lissencephaly and band heterotopia_AGHA_VCGS",
"panel_id": 15,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTB was added\ngene: ACTB was added to Lissencephaly and band heterotopia_AGHA_VCGS. Sources: Australian Genomics Health Alliance Brain Malformations Flagship,Victorian Clinical Genetics Services,Expert Review Green\nMode of inheritance for gene: ACTB was set to Unknown",
"entity_name": "ACTB",
"entity_type": "gene"
}
]
}