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{
"count": 220790,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1984",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1982",
"results": [
{
"created": "2020-01-15T11:57:57.028788+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1592",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Marked gene: HK1 as ready",
"entity_name": "HK1",
"entity_type": "gene"
},
{
"created": "2020-01-15T11:57:57.014732+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1592",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "Gene: hk1 has been classified as Red List (Low Evidence).",
"entity_name": "HK1",
"entity_type": "gene"
},
{
"created": "2020-01-15T11:56:29.639147+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1592",
"user_name": "Natasha Brown",
"item_type": "entity",
"text": "gene: HK1 was added\ngene: HK1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: HK1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: HK1 were set to PMID: 30778173\nMode of pathogenicity for gene: HK1 was set to Other\nReview for gene: HK1 was set to GREEN\nAdded comment: 7 patients from 6 unrelated families with denovo missense variants in the N-terminal half of HK1 \nSources: Literature",
"entity_name": "HK1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:30:39.430272+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STN1 as ready",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:30:39.418635+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:30:36.134947+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STN1 as Amber List (moderate evidence)",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:30:36.123440+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.21",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:30:05.070529+11:00",
"panel_name": "Bone Marrow Failure_VCGS",
"panel_id": 56,
"panel_version": "0.20",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STN1 was added\ngene: STN1 was added to Bone Marrow Failure_VCGS. Sources: Expert list\nMode of inheritance for gene: STN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STN1 were set to 27432940\nPhenotypes for gene: STN1 were set to Cerebroretinal microangiopathy with calcification and cysts 2, MIM#617341\nReview for gene: STN1 was set to AMBER\nAdded comment: Two unrelated individuals reported with a multisystem disorder characterised by premature ageing, pancytopaenia, hypocellular bone marrow, osteopaenia, liver fibrosis, vascular telangiectasia, intracranial calcifications and leukodystrophy. \nSources: Expert list",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:27:23.728226+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STN1 as ready",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:27:23.716866+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:27:13.114964+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STN1 as Amber List (moderate evidence)",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:27:13.103124+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:26:54.537702+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.793",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STN1 was added\ngene: STN1 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: STN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STN1 were set to 27432940\nPhenotypes for gene: STN1 were set to Cerebroretinal microangiopathy with calcification and cysts 2, MIM#617341\nReview for gene: STN1 was set to AMBER\nAdded comment: Two unrelated individuals reported. \nSources: Expert list",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:17:52.402552+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STN1 as ready",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:17:52.382546+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:17:48.656136+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STN1 as Amber List (moderate evidence)",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:17:48.644449+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stn1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:17:14.701956+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: STN1 was added\ngene: STN1 was added to Brain calcification_VCGS. Sources: Expert list\nMode of inheritance for gene: STN1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: STN1 were set to 27432940\nPhenotypes for gene: STN1 were set to Cerebroretinal microangiopathy with calcifications and cysts 2, MIM#\t617341\nReview for gene: STN1 was set to AMBER\nAdded comment: Two individuals from unrelated families described with a multisystem disorder characterized by premature aging, pancytopaenia, hypocellular bone marrow, osteopenia, liver fibrosis, and vascular telangiectasia resulting in gastrointestinal bleeding, as well as intracranial calcifications and leukodystrophy, resulting in spasticity, ataxia, or dystonia. \nSources: Expert list",
"entity_name": "STN1",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:14:38.831635+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SNORD118 as ready",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:14:38.819222+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Green List (High Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:09:56.464962+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1591",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SNORD118 were changed from to Leukoencephalopathy, brain calcifications, and cysts, MIM#614561",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:09:18.317302+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1590",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SNORD118 were set to ",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:08:49.736097+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1589",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SNORD118 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:07:59.536132+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SNORD118 as ready",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:07:59.524774+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Green List (High Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:07:55.831921+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.183",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SNORD118 were changed from to Leukoencephalopathy, brain calcifications, and cysts, MIM#614561",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:07:29.726902+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SNORD118 were set to ",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:07:01.506105+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SNORD118 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:00:49.981587+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SNORD118 as ready",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:00:49.969026+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Green List (High Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:00:40.091779+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SNORD118 as Green List (high evidence)",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T10:00:40.079972+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.10",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: snord118 has been classified as Green List (High Evidence).",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:59:56.800443+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.9",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: SNORD118 was added\ngene: SNORD118 was added to Brain calcification_VCGS. Sources: Expert list\nMode of inheritance for gene: SNORD118 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: SNORD118 were set to 27571260\nPhenotypes for gene: SNORD118 were set to Leukoencephalopathy, brain calcifications, and cysts, MIM#614561\nReview for gene: SNORD118 was set to GREEN\nAdded comment: Over 30 families reported. \nSources: Expert list",
"entity_name": "SNORD118",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:56:04.432641+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FARSB as ready",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:56:04.419065+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: farsb has been classified as Green List (High Evidence).",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:55:40.297322+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FARSB as Green List (high evidence)",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:55:40.284881+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1588",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: farsb has been classified as Green List (High Evidence).",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:55:00.643248+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1587",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FARSB was added\ngene: FARSB was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Expert list\nMode of inheritance for gene: FARSB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FARSB were set to 29573043; 19161147; 29979980; 30014610\nPhenotypes for gene: FARSB were set to Rajab syndrome, MIM#613658; interstitial lung disease; brain calcifications; microcephaly; intellectual disability\nReview for gene: FARSB was set to GREEN\nAdded comment: 7 unrelated families reported. \nSources: Expert list",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:52:39.585653+11:00",
"panel_name": "Pulmonary Fibrosis_VCGS",
"panel_id": 162,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FARSB as ready",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:52:39.574402+11:00",
"panel_name": "Pulmonary Fibrosis_VCGS",
"panel_id": 162,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: farsb has been classified as Green List (High Evidence).",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:52:35.913645+11:00",
"panel_name": "Pulmonary Fibrosis_VCGS",
"panel_id": 162,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FARSB were changed from to Rajab syndrome, MIM#613658; interstitial lung disease; brain calcifications; microcephaly; intellectual disability",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:52:04.472978+11:00",
"panel_name": "Pulmonary Fibrosis_VCGS",
"panel_id": 162,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FARSB were set to ",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:51:40.608187+11:00",
"panel_name": "Pulmonary Fibrosis_VCGS",
"panel_id": 162,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: FARSB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:50:30.189426+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FARSB as ready",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:50:30.176584+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: farsb has been classified as Green List (High Evidence).",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:50:23.143394+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FARSB as Green List (high evidence)",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:50:23.131235+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.8",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: farsb has been classified as Green List (High Evidence).",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:49:03.345181+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: FARSB was added\ngene: FARSB was added to Brain calcification_VCGS. Sources: Expert list\nMode of inheritance for gene: FARSB was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: FARSB were set to 29573043; 19161147; 29979980; 30014610\nPhenotypes for gene: FARSB were set to Rajab syndrome, MIM#613658; interstitial lung disease; brain calcifications; microcephaly; intellectual disability\nReview for gene: FARSB was set to GREEN\nAdded comment: 7 unrelated families reported. \nSources: Expert list",
"entity_name": "FARSB",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:40:35.767811+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AP1S2 as ready",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:40:35.756329+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1s2 has been classified as Green List (High Evidence).",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:40:32.656158+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: AP1S2 as Green List (high evidence)",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:40:32.644504+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ap1s2 has been classified as Green List (High Evidence).",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:40:02.382499+11:00",
"panel_name": "Brain calcification_VCGS",
"panel_id": 58,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AP1S2 was added\ngene: AP1S2 was added to Brain calcification_VCGS. Sources: Expert list\nMode of inheritance for gene: AP1S2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: AP1S2 were set to Mental retardation, X-linked syndromic 5, MIM#304340\nReview for gene: AP1S2 was set to GREEN\nAdded comment: Iron and calcium deposition in the brain is a feature of this condition. \nSources: Expert list",
"entity_name": "AP1S2",
"entity_type": "gene"
},
{
"created": "2020-01-15T09:04:48.371360+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.792",
"user_name": "Anthony Marty",
"item_type": "panel",
"text": "Panel types changed to Victorian Clinical Genetics Services",
"entity_name": null,
"entity_type": null
},
{
"created": "2020-01-15T08:18:40.076659+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GLIS2 as ready",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:18:40.063846+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: glis2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:18:38.521867+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLIS2 were changed from Nephronophthisis 7, OMIM#611498 to Nephronophthisis 7, OMIM#611498",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:18:02.728131+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GLIS2 were changed from to Nephronophthisis 7, OMIM#611498",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:17:21.001206+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GLIS2 were set to ",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:16:39.818956+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GLIS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GLIS2",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:15:31.037390+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: B9D1 as ready",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:15:31.025523+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: b9d1 has been classified as Red List (Low Evidence).",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:15:25.555118+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D1 were changed from Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120 to Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:14:42.459138+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: B9D1 were changed from to Meckel syndrome 9, OMIM #614209; Joubert syndrome 27, OMIM #617120",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:14:06.933780+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: B9D1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "B9D1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:12:57.720047+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EVC as ready",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:12:57.708337+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: evc has been classified as Red List (Low Evidence).",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:12:51.866918+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EVC were changed from Ellis-van Creveld syndrome, MIM#225500 to Ellis-van Creveld syndrome, MIM#225500",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:12:05.648040+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EVC were changed from to Ellis-van Creveld syndrome, MIM#225500",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:11:23.861403+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.86",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EVC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EVC",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:10:20.415847+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FOXC1 as ready",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:10:20.403592+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: foxc1 has been classified as Red List (Low Evidence).",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:10:10.675840+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.85",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FOXC1 were changed from to Axenfeld-Rieger syndrome, type 3, MIM#602482",
"entity_name": "FOXC1",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:08:51.661441+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: IFT57 as ready",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:08:51.649317+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ift57 has been classified as Red List (Low Evidence).",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:08:46.654822+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.84",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT57 were changed from Orofaciodigital syndrome XVIII, MIM#617927 to Orofaciodigital syndrome XVIII, MIM#617927",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:07:54.443061+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.83",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: IFT57 were changed from to Orofaciodigital syndrome XVIII, MIM#617927",
"entity_name": "IFT57",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:06:23.590788+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KIF14 as ready",
"entity_name": "KIF14",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:06:23.579385+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kif14 has been classified as Red List (Low Evidence).",
"entity_name": "KIF14",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:05:55.901000+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.82",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from Joubert syndrome 22, OMIM #615665 to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:05:55.776081+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDE6D as ready",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:05:55.763081+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pde6d has been classified as Red List (Low Evidence).",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:05:04.206587+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDE6D were changed from to Joubert syndrome 22, OMIM #615665",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:04:28.546182+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.81",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDE6D were set to ",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:03:39.980855+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.80",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDE6D was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PDE6D",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:02:36.803752+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: POC1B was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:02:36.753403+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: POC1B as ready",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:02:36.739935+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: poc1b has been classified as Red List (Low Evidence).",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:01:55.668216+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.79",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: POC1B was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:01:12.449250+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: POC1B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T08:00:36.126816+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.78",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: POC1B were changed from to Cone-rod dystrophy 20, MIM#615973",
"entity_name": "POC1B",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:58:50.198653+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SLC41A1 as ready",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:58:50.186816+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: slc41a1 has been classified as Red List (Low Evidence).",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:58:40.521847+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.77",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SLC41A1 were changed from to Nephronophthisis; no OMIM number",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:58:03.319420+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: SLC41A1 were set to ",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:57:22.088997+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.76",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SLC41A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SLC41A1",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:56:16.636145+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WDR34 as ready",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:56:16.622965+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wdr34 has been classified as Red List (Low Evidence).",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:56:13.279082+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.75",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR34 were changed from Short-rib thoracic dysplasia 11 with or without polydactyly, OMIM #615633 to Short-rib thoracic dysplasia 11 with or without polydactyly, OMIM #615633",
"entity_name": "WDR34",
"entity_type": "gene"
},
{
"created": "2020-01-15T07:55:27.819078+11:00",
"panel_name": "Renal ciliopathies and nephronophthisis_KidGen_VCGS",
"panel_id": 193,
"panel_version": "0.74",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WDR34 were changed from to Short-rib thoracic dysplasia 11 with or without polydactyly, OMIM #615633",
"entity_name": "WDR34",
"entity_type": "gene"
}
]
}