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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2081",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2079",
"results": [
{
"created": "2019-11-30T11:26:14.922080+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.65",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ctnna2 has been classified as Green List (High Evidence).",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:25:52.984453+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.64",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: CTNNA2 was added\ngene: CTNNA2 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: CTNNA2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CTNNA2 were set to 30013181\nPhenotypes for gene: CTNNA2 were set to Cortical dysplasia, complex, with other brain malformations 9, MIM#618174\nReview for gene: CTNNA2 was set to GREEN\nAdded comment: 13 children from three unrelated families reported, severe ID as part of the phenotype. \nSources: Expert list",
"entity_name": "CTNNA2",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:14:17.719440+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRTAP as ready",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:14:17.712523+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crtap has been classified as Red List (Low Evidence).",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:14:13.073679+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.63",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRTAP were changed from to Osteogenesis imperfecta, type VII, MIM#610682",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:13:58.562752+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.62",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRTAP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:13:47.478069+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CRTAP as Red List (low evidence)",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:13:47.471104+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.61",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crtap has been classified as Red List (Low Evidence).",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:13:34.612752+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRTAP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Osteogenesis imperfecta, type VII, MIM#610682; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CRTAP",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:43.239702+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRLF1 as ready",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:43.228185+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crlf1 has been classified as Red List (Low Evidence).",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:28.333495+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.60",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CRLF1 were changed from to Cold-induced sweating syndrome 1, MIM#272430",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:16.596774+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.59",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRLF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:05.366131+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CRLF1 as Red List (low evidence)",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:10:05.356048+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.58",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crlf1 has been classified as Red List (Low Evidence).",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T11:09:52.674744+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRLF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cold-induced sweating syndrome 1, MIM#272430; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CRLF1",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:45.724583+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CRKL as ready",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:45.717586+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crkl has been classified as Red List (Low Evidence).",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:40.637488+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.57",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CRKL were set to ",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:31.123251+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CRKL was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:23.799485+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CRKL as Red List (low evidence)",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:23.791041+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: crkl has been classified as Red List (Low Evidence).",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:29:03.610748+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CRKL: Rating: RED; Mode of pathogenicity: None; Publications: 28121514, 25565927; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CRKL",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:24:48.705855+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CPA6: Rating: GREEN; Mode of pathogenicity: None; Publications: 25875328, 21922598, 23105115; Phenotypes: Epilepsy, familial temporal lobe, 5, MIM#614417, Febrile seizures, familial, 11, MIM#614418; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:23:49.141773+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CPA6 as ready",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:23:49.134436+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cpa6 has been classified as Red List (Low Evidence).",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:23:37.163695+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.54",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CPA6 were changed from to Epilepsy, familial temporal lobe, 5, MIM#614417; Febrile seizures, familial, 11, MIM#614418",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:23:27.368983+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.53",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CPA6 were set to ",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:23:02.492241+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.52",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CPA6 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:51.952494+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CPA6 as Red List (low evidence)",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:51.943781+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.51",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cpa6 has been classified as Red List (Low Evidence).",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:33.156369+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CPA6 as ready",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:33.148885+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cpa6 has been classified as Green List (High Evidence).",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:27.358530+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CPA6 were changed from to Epilepsy, familial temporal lobe, 5, MIM#614417; Febrile seizures, familial, 11, MIM#614418",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:22:02.344175+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.13",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CPA6 were set to ",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:21:29.484062+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.12",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CPA6 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:20:59.887980+11:00",
"panel_name": "Genetic Epilepsy_AustralianGenomics_VCGS",
"panel_id": 202,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CPA6: Rating: GREEN; Mode of pathogenicity: None; Publications: 25875328, 21922598, 23105115; Phenotypes: Epilepsy, familial temporal lobe, 5, MIM#614417, Febrile seizures, familial, 11, MIM#614418; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:19:54.714568+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CPA6: Rating: RED; Mode of pathogenicity: None; Publications: 25875328, 21922598, 23105115; Phenotypes: Epilepsy, familial temporal lobe, 5, MIM#614417, Febrile seizures, familial, 11, MIM#614418; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CPA6",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:13:32.204420+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CP as ready",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:13:32.197290+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cp has been classified as Green List (High Evidence).",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:13:28.356132+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CP was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:12:48.173155+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CP were changed from to Aceruloplasminaemia, MIM#604290",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:12:30.342942+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:12:00.226871+11:00",
"panel_name": "Regression_VCGS",
"panel_id": 206,
"panel_version": "0.14",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aceruloplasminaemia, MIM#604290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:11:32.960247+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CP as ready",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:11:32.952821+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cp has been classified as Green List (High Evidence).",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:11:22.867183+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CP were changed from to Aceruloplasminaemia, MIM#604290",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:11:11.523909+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:10:45.269725+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aceruloplasminaemia, MIM#604290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:08:54.683812+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CP as ready",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:08:54.676702+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cp has been classified as Green List (High Evidence).",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:08:50.095916+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.4",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CP were changed from to Aceruloplasminaemia, MIM#604290",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:08:27.991869+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.3",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:08:00.830531+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aceruloplasminaemia, MIM#604290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:01:26.412924+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CP as ready",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:01:26.405806+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cp has been classified as Red List (Low Evidence).",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:01:20.193287+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.50",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CP were changed from to Aceruloplasminaemia, MIM#604290",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:01:06.183727+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.49",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:00:44.450940+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CP as Red List (low evidence)",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:00:44.443485+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.48",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cp has been classified as Red List (Low Evidence).",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T09:00:26.515490+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Aceruloplasminaemia, MIM#604290; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CP",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:50:21.784993+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX7B as ready",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:50:21.777606+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox7b has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:50:17.495062+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.47",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX7B were changed from to Linear skin defects with multiple congenital anomalies 2, MIM#300887",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:50:00.574221+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.46",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX7B were set to ",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:49:41.156353+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX7B as Amber List (moderate evidence)",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:49:41.148813+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.45",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox7b has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-30T07:49:26.849375+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX7B: Rating: AMBER; Mode of pathogenicity: None; Publications: 23122588; Phenotypes: Linear skin defects with multiple congenital anomalies 2, MIM#300887; Mode of inheritance: Other",
"entity_name": "COX7B",
"entity_type": "gene"
},
{
"created": "2019-11-29T20:31:43.517286+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX4I2 as ready",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T20:31:43.509394+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i2 has been classified as Green List (High Evidence).",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T20:31:35.195766+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX4I2 were changed from to Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, MIM#612714",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T20:31:17.190344+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX4I2 were set to ",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T20:31:00.332364+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COX4I2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:17:00.218077+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX4I2 as ready",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:17:00.210172+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i2 has been classified as Red List (Low Evidence).",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:16:55.648693+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.44",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX4I2 were changed from to Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, MIM#612714",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:16:44.474875+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.11",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX4I2: Rating: GREEN; Mode of pathogenicity: None; Publications: 19268275, 22730437; Phenotypes: Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, MIM#612714; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:16:16.790420+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.43",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX4I2 were set to ",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:14:57.442469+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX4I2 as Red List (low evidence)",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:14:57.434331+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.42",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox4i2 has been classified as Red List (Low Evidence).",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:14:42.334746+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX4I2: Rating: RED; Mode of pathogenicity: None; Publications: 19268275, 22730437; Phenotypes: Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis, MIM#612714; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX4I2",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:05:41.804065+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX20 as ready",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:05:41.796426+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:05:29.957095+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.41",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX20 were changed from to Mitochondrial complex IV deficiency, MIM#220110",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:05:15.280571+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.40",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: COX20 were set to ",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:04:58.615712+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.39",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: COX20 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:04:46.687219+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: COX20 as Amber List (moderate evidence)",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:04:46.678742+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.38",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox20 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T19:04:19.332030+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.37",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: COX20: Rating: RED; Mode of pathogenicity: None; Publications: 31079202, 30656193, 24202787; Phenotypes: Mitochondrial complex IV deficiency, MIM#220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "COX20",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:10:31.905767+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDIA2 as ready",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:10:31.898402+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdia2 has been classified as Red List (Low Evidence).",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:10:24.863089+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDIA2 were changed from to Bicuspid aortic valve",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:10:03.263293+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDIA2 were set to ",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:09:49.152083+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: PDIA2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:09:32.128527+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PDIA2 as Red List (low evidence)",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:09:32.120330+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdia2 has been classified as Red List (Low Evidence).",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T14:09:11.465526+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PDIA2: Rating: RED; Mode of pathogenicity: None; Publications: 20098615; Phenotypes: Bicuspid aortic valve; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "PDIA2",
"entity_type": "gene"
},
{
"created": "2019-11-29T13:38:49.687701+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: COX14 as ready",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2019-11-29T13:38:49.680398+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cox14 has been classified as Amber List (Moderate Evidence).",
"entity_name": "COX14",
"entity_type": "gene"
},
{
"created": "2019-11-29T13:38:41.522777+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: COX14 were changed from to Mitochondrial complex IV deficiency, MIM#220110",
"entity_name": "COX14",
"entity_type": "gene"
}
]
}