HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2063",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2061",
"results": [
{
"created": "2019-12-07T11:38:16.693639+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfhr1 has been classified as Red List (Low Evidence).",
"entity_name": "CFHR1",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:38:12.374495+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.794",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFHR1 were changed from to Hemolytic uremic syndrome, atypical, susceptibility to, MIM#235400",
"entity_name": "CFHR1",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:52.593646+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.793",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CFHR1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CFHR1",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:43.706867+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CFHR1 as Red List (low evidence)",
"entity_name": "CFHR1",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:43.699356+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.792",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfhr1 has been classified as Red List (Low Evidence).",
"entity_name": "CFHR1",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:06.208273+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFH as ready",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:06.201216+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfh has been classified as Red List (Low Evidence).",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:37:01.776346+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.791",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFH were changed from to Complement factor H deficiency, MIM#609814",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:49.017165+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.790",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CFH was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:37.785124+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CFH as Red List (low evidence)",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:37.777608+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.789",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfh has been classified as Red List (Low Evidence).",
"entity_name": "CFH",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:05.969878+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP89 as ready",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:05.962421+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep89 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:36:01.421339+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.788",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP89 were changed from to Mitochondrial complex IV deficiency",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:35:40.872860+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.787",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP89 were set to ",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:35:30.987239+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.786",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP89 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:35:24.483374+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CEP89 as Amber List (moderate evidence)",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:35:24.475340+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.785",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep89 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CEP89",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:34:25.069666+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CEP63 as ready",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:34:25.062057+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep63 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:34:19.627571+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.784",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CEP63 were changed from to Seckel syndrome 6, MIM#614728",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:34:06.772588+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.783",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CEP63 were set to ",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:33:52.872871+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.782",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CEP63 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:33:45.679645+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CEP63 as Amber List (moderate evidence)",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:33:45.669559+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.781",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cep63 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CEP63",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:57:32.707463+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.172",
"user_name": "Seb L",
"item_type": "entity",
"text": "Marked gene: WDR91 as ready",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:57:32.698654+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.172",
"user_name": "Seb L",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Red List (Low Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:56:21.996543+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.172",
"user_name": "Seb L",
"item_type": "entity",
"text": "Classified gene: WDR91 as Red List (low evidence)",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:56:21.989042+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.172",
"user_name": "Seb L",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Red List (Low Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:52:14.025219+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia_VCGS",
"panel_id": 72,
"panel_version": "0.2",
"user_name": "Seb L",
"item_type": "entity",
"text": "Classified gene: WDR91 as Red List (low evidence)",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:52:14.010808+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia_VCGS",
"panel_id": 72,
"panel_version": "0.2",
"user_name": "Seb L",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Red List (Low Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:51:40.295310+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia_VCGS",
"panel_id": 72,
"panel_version": "0.1",
"user_name": "Seb L",
"item_type": "entity",
"text": "Marked gene: WDR91 as ready",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:51:40.286597+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia_VCGS",
"panel_id": 72,
"panel_version": "0.1",
"user_name": "Seb L",
"item_type": "entity",
"text": "Gene: wdr91 has been classified as Green List (High Evidence).",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T09:51:19.560316+11:00",
"panel_name": "Cerebellar and Pontocerebellar hypoplasia_VCGS",
"panel_id": 72,
"panel_version": "0.1",
"user_name": "Seb L",
"item_type": "entity",
"text": "reviewed gene: WDR91: Rating: RED; Mode of pathogenicity: None; Publications: 28969387; Phenotypes: ; Mode of inheritance: Unknown",
"entity_name": "WDR91",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:46.821065+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDT1 as ready",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:46.813743+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdt1 has been classified as Red List (Low Evidence).",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:41.936988+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.780",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDT1 were changed from to Meier-Gorlin syndrome 4, MIM#613804",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:28.995329+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.779",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:21.362126+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CDT1 as Red List (low evidence)",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:23:21.355371+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.778",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdt1 has been classified as Red List (Low Evidence).",
"entity_name": "CDT1",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:22:38.072711+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDK6 as ready",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:22:38.065822+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:22:32.711017+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.777",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDK6 were changed from to Microcephaly 12, primary, autosomal recessive, MIM#616080",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:22:16.866206+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.776",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CDK6 were set to ",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:22:01.788370+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.775",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDK6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:21:49.567581+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CDK6 as Amber List (moderate evidence)",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:21:49.560402+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK6",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:21:04.009568+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDK16 as ready",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:21:04.000316+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:20:54.253315+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CDK16 as Amber List (moderate evidence)",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:20:54.245714+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.170",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:20:33.920603+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.169",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CDK16 was added\ngene: CDK16 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: CDK16 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: CDK16 were set to 25644381\nPhenotypes for gene: CDK16 were set to Intellectual disability\nReview for gene: CDK16 was set to AMBER\nAdded comment: Single family described in this manuscript describing multiple candidate genes for XLID. \nSources: Expert list",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:16:15.191243+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CDK16 as ready",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:16:15.184051+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:16:10.483152+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CDK16 were changed from to Intellectual disability",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:15:52.818008+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CDK16 were set to ",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:15:39.156117+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CDK16 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:15:25.474642+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CDK16 as Amber List (moderate evidence)",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:15:25.465160+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cdk16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CDK16",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:48.943935+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CD96 as ready",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:48.936416+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd96 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:44.547347+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CD96 were changed from to C syndrome, MIM#211750",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:32.122259+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CD96 were set to ",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:19.904823+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CD96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:07.161391+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CD96 as Amber List (moderate evidence)",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-07T07:14:07.153089+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cd96 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CD96",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:38:31.404359+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CCDC8 as ready",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:38:31.397054+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc8 has been classified as Red List (Low Evidence).",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:38:26.709004+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CCDC8 were changed from to 3-M syndrome 3, MIM#614205",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:38:17.893727+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CCDC8 were set to ",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:38:08.892032+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCDC8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:58.117201+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CCDC8 as Red List (low evidence)",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:58.109681+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc8 has been classified as Red List (Low Evidence).",
"entity_name": "CCDC8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:24.620479+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CCDC78 as ready",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:24.613282+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc78 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:19.850442+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CCDC78 were changed from to Centronuclear myopathy 4, MIM#614807",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:37:07.334885+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CCDC78 were set to ",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:58.655452+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CCDC78 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:47.892790+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CCDC78 as Amber List (moderate evidence)",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:47.877347+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ccdc78 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CCDC78",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:16.522975+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNA1G as ready",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:16.515818+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1g has been classified as Green List (High Evidence).",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:36:11.891715+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CACNA1G were changed from to Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits, MIM#618087",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:35:59.471178+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.756",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CACNA1G were set to ",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:35:50.327140+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CACNA1G was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CACNA1G",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:35:13.953930+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CA8 as ready",
"entity_name": "CA8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:35:13.946744+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ca8 has been classified as Green List (High Evidence).",
"entity_name": "CA8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:35:09.630566+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CA8 were changed from to Cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3, MIM#613227",
"entity_name": "CA8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:34:56.384274+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CA8 were set to ",
"entity_name": "CA8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:34:43.004193+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CA8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CA8",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:34:13.959518+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CA2 as ready",
"entity_name": "CA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:34:13.951660+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ca2 has been classified as Green List (High Evidence).",
"entity_name": "CA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:34:09.198121+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CA2 were changed from to Osteopetrosis, autosomal recessive 3, with renal tubular acidosis, MIM#259730",
"entity_name": "CA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:33:56.074207+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CA2",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:43.823741+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: C3orf58 as ready",
"entity_name": "C3orf58",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:43.816517+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c3orf58 has been classified as Red List (Low Evidence).",
"entity_name": "C3orf58",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:38.791170+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: C3orf58 as Red List (low evidence)",
"entity_name": "C3orf58",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:38.782660+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c3orf58 has been classified as Red List (Low Evidence).",
"entity_name": "C3orf58",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:00.516212+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: C19orf12 as ready",
"entity_name": "C19orf12",
"entity_type": "gene"
},
{
"created": "2019-12-06T21:07:00.509028+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: c19orf12 has been classified as Red List (Low Evidence).",
"entity_name": "C19orf12",
"entity_type": "gene"
}
]
}