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{
"count": 220423,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2049",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2047",
"results": [
{
"created": "2019-12-11T14:50:54.270704+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1283",
"user_name": "chirag patel",
"item_type": "entity",
"text": "gene: TARS was added\ngene: TARS was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: TARS was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TARS were set to PMID: 31374204\nPhenotypes for gene: TARS were set to Trichothiodystrophy 7, nonphotosensitive; OMIM #618546\nReview for gene: TARS was set to AMBER\nAdded comment: Clinical features of trichothiodystrophy (TTD) include ichthyosis, intellectual disability, decreased fertility, short stature.\r\n\r\n2 unrelated patients with non-photosensitive-TTD, in whom limited clinical information was available (one with DD): one compound heterozygous TARS variants, second homozygous for TARS variant. They showed that the variants had a profound effect on TARS protein stability and enzymatic function. \nSources: Literature",
"entity_name": "TARS",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:49:34.176194+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APC2 as ready",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:49:34.168951+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:49:29.524394+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: APC2 as Green List (high evidence)",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:49:29.516067+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.7",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:49:01.732325+11:00",
"panel_name": "Lissencephaly and band heterotopia_AustralianGenomics_VCGS",
"panel_id": 15,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: APC2 was added\ngene: APC2 was added to Lissencephaly and band heterotopia_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: APC2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: APC2 were set to 31585108\nPhenotypes for gene: APC2 were set to Cortical dysplasia, complex, with other brain malformations 10, MIM#618677\nAdded comment: 12 individuals from 8 unrelated families; intellectual disability, seizures, cortical dysplasia including posterior to anterior predominant pattern of lissencephaly, heterotopias, paucity of white matter, thin corpus callosum. \nSources: Literature",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:47:31.854543+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APC2 as ready",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:47:31.847072+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:47:21.903601+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: APC2 as Green List (high evidence)",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:47:21.895417+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:47:02.957993+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: APC2 was added\ngene: APC2 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: APC2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: APC2 were set to 31585108\nPhenotypes for gene: APC2 were set to Cortical dysplasia, complex, with other brain malformations 10, MIM#618677\nReview for gene: APC2 was set to GREEN\nAdded comment: 12 individuals from 8 unrelated families; intellectual disability, seizures, cortical dysplasia including posterior to anterior predominant pattern of lissencephaly, heterotopias, paucity of white matter, thin corpus callosum. \nSources: Literature",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:44:05.440636+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1282",
"user_name": "chirag patel",
"item_type": "entity",
"text": "changed review comment from: 3 unrelated families, but no functional evidence. \nSources: Literature; to: 3 unrelated families with DD/ID as part of syndromic microphthalmia, but no functional evidence. \r\nSources: Literature",
"entity_name": "TEMN3-AS1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:43:37.355496+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1282",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: TEMN3-AS1 as Amber List (moderate evidence)",
"entity_name": "TEMN3-AS1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:43:37.348320+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1282",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: temn3-as1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TEMN3-AS1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:43:26.427494+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1281",
"user_name": "chirag patel",
"item_type": "entity",
"text": "gene: TEMN3-AS1 was added\ngene: TEMN3-AS1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: TEMN3-AS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TEMN3-AS1 were set to PubMed: 27103084; 30513139; 30513139\nPhenotypes for gene: TEMN3-AS1 were set to ?Microphthalmia, isolated, with coloboma 9, OMIM #615145; Microphthalmia, syndromic 15, OMIM #615145\nReview for gene: TEMN3-AS1 was set to AMBER\nAdded comment: 3 unrelated families, but no functional evidence. \nSources: Literature",
"entity_name": "TEMN3-AS1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:39:49.300542+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: APC2 as ready",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:39:49.293149+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:39:43.698756+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: APC2 as Green List (high evidence)",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:39:43.691055+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1280",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: apc2 has been classified as Green List (High Evidence).",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:39:28.943736+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1279",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: APC2 was added\ngene: APC2 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: APC2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: APC2 were set to 31585108\nPhenotypes for gene: APC2 were set to Cortical dysplasia, complex, with other brain malformations 10, MIM#618677\nReview for gene: APC2 was set to GREEN\nAdded comment: 12 individuals from 8 unrelated families; intellectual disability, seizures, cortical dysplasia including posterior to anterior predominant pattern of lissencephaly, heterotopias, paucity of white matter, thin corpus callosum. \nSources: Literature",
"entity_name": "APC2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:36:15.832355+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1278",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: VAMP2 as Green List (high evidence)",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:36:15.825229+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1278",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: vamp2 has been classified as Green List (High Evidence).",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:35:46.372133+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1277",
"user_name": "chirag patel",
"item_type": "entity",
"text": "gene: VAMP2 was added\ngene: VAMP2 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: VAMP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: VAMP2 were set to PMID: 30929742\nPhenotypes for gene: VAMP2 were set to no OMIM number yet\nReview for gene: VAMP2 was set to GREEN\nAdded comment: 5 unrelated patients with heterozygous de novo mutations in VAMP2, presenting with a neurodevelopmental disorder characterized by axial hypotonia, intellectual disability, and autistic features. Affected individuals carrying de novo non-synonymous variants involving the C-terminal region presented a more severe phenotype with additional neurological features, including central visual impairment, hyperkinetic movement disorder, and epilepsy or electroencephalography abnormalities. Reconstituted fusion involving a lipid-mixing assay indicated impairment in vesicle fusion as one of the possible associated disease mechanisms. \nSources: Literature",
"entity_name": "VAMP2",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:31:01.705198+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1276",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: ZMIZ1 as Green List (high evidence)",
"entity_name": "ZMIZ1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:31:01.696936+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1276",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: zmiz1 has been classified as Green List (High Evidence).",
"entity_name": "ZMIZ1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:30:48.657341+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1275",
"user_name": "chirag patel",
"item_type": "entity",
"text": "gene: ZMIZ1 was added\ngene: ZMIZ1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: ZMIZ1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ZMIZ1 were set to PubMed: 30639322\nPhenotypes for gene: ZMIZ1 were set to Neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies; OMIM #618659\nReview for gene: ZMIZ1 was set to GREEN\nAdded comment: 28 families with spectrum of neurodevelopmental features (including ID, ASD, and ADHD) due to de novo ZNF292 variants (1 family inherited). No functional evidence of specific variants, but ZNF292 is highly expressed in the developing human brain.\r\n\r\n\r\n14 unrelated patients with neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies, and de novo heterozygous mutations in the ZMIZ1 gene. Transfection of 3 variants (T300M, c.3112dupA, and K91R) into HEK293T cells resulted in decreased induction of luciferase activity compared to wildtype (although the change for K91R was not statistically significant), suggesting impaired coactivation activity of the mutant proteins. Electroporation of these 3 mutants into progenitor cells in the ventricular zone of embryonic mice cortices resulted in defective neuronal migration to the cortex, as well as morphologic abnormalities of the neurons manifest as rounded cells with aberrantly oriented processes. These findings suggested that the ZMIZ1 mutations disrupted proper neuronal polarization and neuronal migration in the developing cortex. Functional studies of the other variants and additional studies of patient cells were not performed. \nSources: Literature",
"entity_name": "ZMIZ1",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:24:21.431503+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1274",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Classified gene: ZNF292 as Green List (high evidence)",
"entity_name": "ZNF292",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:24:21.424005+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1274",
"user_name": "chirag patel",
"item_type": "entity",
"text": "Gene: znf292 has been classified as Green List (High Evidence).",
"entity_name": "ZNF292",
"entity_type": "gene"
},
{
"created": "2019-12-11T14:24:08.117765+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1273",
"user_name": "chirag patel",
"item_type": "entity",
"text": "gene: ZNF292 was added\ngene: ZNF292 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: ZNF292 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ZNF292 were set to PMID: 31723249\nPhenotypes for gene: ZNF292 were set to no OMIM number yet\nReview for gene: ZNF292 was set to GREEN\nAdded comment: 28 families with spectrum of neurodevelopmental features (including ID, ASD, and ADHD) due to de novo ZNF292 variants (1 family inherited). No functional evidence of specific variants, but ZNF292 is highly expressed in the developing human brain. \nSources: Literature",
"entity_name": "ZNF292",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:19:58.256088+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALKBH8 as ready",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:19:58.248144+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alkbh8 has been classified as Green List (High Evidence).",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:19:48.321385+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALKBH8 as Green List (high evidence)",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:19:48.313188+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alkbh8 has been classified as Green List (High Evidence).",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:19:29.164070+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ALKBH8 was added\ngene: ALKBH8 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: ALKBH8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ALKBH8 were set to 31079898\nPhenotypes for gene: ALKBH8 were set to Intellectual developmental disorder, autosomal recessive 71, MIM#618504\nReview for gene: ALKBH8 was set to GREEN\nAdded comment: Two families and functional data. \nSources: Literature",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:16:30.646864+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ALKBH8 as ready",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:16:30.639314+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alkbh8 has been classified as Green List (High Evidence).",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:16:14.764137+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ALKBH8 as Green List (high evidence)",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:16:14.755746+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1272",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: alkbh8 has been classified as Green List (High Evidence).",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:16:00.535865+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1271",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ALKBH8 was added\ngene: ALKBH8 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: ALKBH8 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ALKBH8 were set to 31079898\nPhenotypes for gene: ALKBH8 were set to Intellectual developmental disorder, autosomal recessive 71, MIM#618504\nReview for gene: ALKBH8 was set to GREEN\nAdded comment: Two families and functional data. \nSources: Literature",
"entity_name": "ALKBH8",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:12:08.131932+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADGRB3 as ready",
"entity_name": "ADGRB3",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:12:08.124367+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adgrb3 has been classified as Red List (Low Evidence).",
"entity_name": "ADGRB3",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:11:58.366318+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1270",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADGRB3 was added\ngene: ADGRB3 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: ADGRB3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ADGRB3 were set to 30659260; 18628273\nPhenotypes for gene: ADGRB3 were set to Intellectual disability\nReview for gene: ADGRB3 was set to RED\nAdded comment: Single family with intragenic bi-allelic duplications and ID reported; association studies with schizophrenia. \nSources: Literature",
"entity_name": "ADGRB3",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:05:50.778335+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACTL6B as ready",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:05:50.770166+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:05:38.019376+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ACTL6B as Green List (high evidence)",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:05:38.012113+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:05:17.238308+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTL6B was added\ngene: ACTL6B was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: ACTL6B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ACTL6B were set to 31134736; 31031012; 30656450; 30237576\nPhenotypes for gene: ACTL6B were set to Epileptic encephalopathy, early infantile, 76, MIM#\t618468; Intellectual developmental disorder with severe speech and ambulation defects, MIM#\t618470\nReview for gene: ACTL6B was set to GREEN\nAdded comment: Over 10 unrelated individuals reported in the literature. \nSources: Literature",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:00:06.693843+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACTL6B as ready",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:00:06.686146+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:00:02.167474+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ACTL6B as Green List (high evidence)",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T13:00:02.150463+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:59:27.443790+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTL6B was added\ngene: ACTL6B was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: ACTL6B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ACTL6B were set to 31134736; 31031012; 30656450; 30237576\nPhenotypes for gene: ACTL6B were set to Epileptic encephalopathy, early infantile, 76, MIM#\t618468; Intellectual developmental disorder with severe speech and ambulation defects, MIM#\t618470\nReview for gene: ACTL6B was set to GREEN\nAdded comment: Multiple affected individuals reported, main phenotype is ID/EE. \nSources: Literature",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:57:09.725332+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ACTL6B as ready",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:57:09.717981+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:57:04.402748+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ACTL6B as Green List (high evidence)",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:57:04.395346+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1269",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: actl6b has been classified as Green List (High Evidence).",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:56:47.604115+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1268",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ACTL6B was added\ngene: ACTL6B was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: ACTL6B was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ACTL6B were set to 31134736; 31031012; 30656450; 30237576\nPhenotypes for gene: ACTL6B were set to Epileptic encephalopathy, early infantile, 76, MIM#\t618468; Intellectual developmental disorder with severe speech and ambulation defects, MIM#\t618470\nReview for gene: ACTL6B was set to GREEN\nAdded comment: Multiple affected individuals reported, main phenotype is ID/EE. \nSources: Literature",
"entity_name": "ACTL6B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:37:19.682291+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SP7 as ready",
"entity_name": "SP7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:37:19.674641+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sp7 has been classified as Red List (Low Evidence).",
"entity_name": "SP7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:37:15.367598+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1267",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: SP7 were changed from to Osteogenesis imperfecta, type XII; OMIM # 613849",
"entity_name": "SP7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:37:04.145840+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1266",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SP7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "SP7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:36:16.197752+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPEG as ready",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:36:16.189562+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: speg has been classified as Red List (Low Evidence).",
"entity_name": "SPEG",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:33:49.697224+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPINK5 as ready",
"entity_name": "SPINK5",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:33:49.690217+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spink5 has been classified as Red List (Low Evidence).",
"entity_name": "SPINK5",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:32:37.033438+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPTLC1 as ready",
"entity_name": "SPTLC1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:32:37.026514+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: sptlc1 has been classified as Red List (Low Evidence).",
"entity_name": "SPTLC1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:32:30.558490+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: SPTLC1 was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "SPTLC1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:31:17.505002+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ST7 as ready",
"entity_name": "ST7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:31:17.497614+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: st7 has been classified as Red List (Low Evidence).",
"entity_name": "ST7",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:30:03.460561+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAC3 as ready",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:30:03.431517+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stac3 has been classified as Red List (Low Evidence).",
"entity_name": "STAC3",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:29:05.353670+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STAT5B as ready",
"entity_name": "STAT5B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:29:05.345108+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stat5b has been classified as Red List (Low Evidence).",
"entity_name": "STAT5B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:27:13.990434+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STK3 as ready",
"entity_name": "STK3",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:27:13.982104+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stk3 has been classified as Red List (Low Evidence).",
"entity_name": "STK3",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:25:17.369458+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1264",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STT3A were changed from ?Congenital disorder of glycosylation, type Iw; OMIM #615596 to Congenital disorder of glycosylation, type Iw; OMIM #615596",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:24:49.634808+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1263",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STT3A were set to PMID: 23842455",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:24:34.899982+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STT3A as Green List (high evidence)",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:24:34.896693+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Two further recent publications identified, bringing the total number of reported families to three.",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:24:34.863084+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1262",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stt3a has been classified as Green List (High Evidence).",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:23:48.861485+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STT3A as ready",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:23:48.853386+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stt3a has been classified as Green List (High Evidence).",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:23:45.224810+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: STT3A were changed from to Congenital disorder of glycosylation, type Iw; OMIM #615596",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:23:19.130687+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: STT3A were set to ",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:22:56.294690+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: STT3A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:22:29.693699+11:00",
"panel_name": "Congenital Disorders of Glycosylation_VCGS",
"panel_id": 68,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: STT3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23842455, 30701557, 28424003; Phenotypes: Congenital disorder of glycosylation, type Iw, OMIM #615596; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:17:24.966341+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STT3A as ready",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:17:24.958427+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stt3a has been classified as Red List (Low Evidence).",
"entity_name": "STT3A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:10:18.263893+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STT3B as ready",
"entity_name": "STT3B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:10:18.255973+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stt3b has been classified as Red List (Low Evidence).",
"entity_name": "STT3B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:09:37.421869+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TAF8 as ready",
"entity_name": "TAF8",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:09:37.414705+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: taf8 has been classified as Red List (Low Evidence).",
"entity_name": "TAF8",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:08:30.446384+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TDGF1 as ready",
"entity_name": "TDGF1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:08:30.439304+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tdgf1 has been classified as Red List (Low Evidence).",
"entity_name": "TDGF1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:08:24.386612+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1261",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TDGF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "TDGF1",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:07:26.124248+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TFAP2A as ready",
"entity_name": "TFAP2A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:07:26.117234+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tfap2a has been classified as Red List (Low Evidence).",
"entity_name": "TFAP2A",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:06:48.797258+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TFAP2B as ready",
"entity_name": "TFAP2B",
"entity_type": "gene"
},
{
"created": "2019-12-11T12:06:48.790247+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ_VCGS",
"panel_id": 250,
"panel_version": "0.1260",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tfap2b has been classified as Red List (Low Evidence).",
"entity_name": "TFAP2B",
"entity_type": "gene"
}
]
}