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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2079",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2077",
"results": [
{
"created": "2019-12-01T18:03:15.696127+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.123",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DSE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:03:08.425748+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DSE as Red List (low evidence)",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:03:08.418329+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.122",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dse has been classified as Red List (Low Evidence).",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:02:54.794367+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DSE: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ehlers-Danlos syndrome, musculocontractural type 2, MIM#615539; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:31:39.165776+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DPYS as ready",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:31:39.158441+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dpys has been classified as Green List (High Evidence).",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:31:29.666919+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DPYS were changed from to Dihydropyrimidinuria, MIM#222748",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:31:12.757648+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DPYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:30:52.575565+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DPYS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dihydropyrimidinuria, MIM#222748; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:28:28.540976+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DPYS as ready",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:28:28.533405+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dpys has been classified as Green List (High Evidence).",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:28:20.583383+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.121",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DPYS were changed from to Dihydropyrimidinuria, MIM#222748",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:28:09.124949+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.120",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DPYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:27:50.579184+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DPYS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dihydropyrimidinuria, MIM#222748; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPYS",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:25:19.723752+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: DPP10: Added comment: Link to autism based on CNV data.; Changed publications: 28670437",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:24:19.500029+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DPP10 as ready",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:24:19.492272+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dpp10 has been classified as Red List (Low Evidence).",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:24:13.874029+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.119",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DPP10 were set to ",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:23:58.055477+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DPP10 as Red List (low evidence)",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:23:58.047775+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.118",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dpp10 has been classified as Red List (Low Evidence).",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:23:22.261087+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DPP10: Rating: RED; Mode of pathogenicity: None; Publications: 28670437; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DPP10",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:17:23.165712+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DPH1 as ready",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:17:23.157944+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dph1 has been classified as Green List (High Evidence).",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:17:16.505150+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.117",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DPH1 were changed from to Developmental delay with short stature, dysmorphic facial features, and sparse hair, MIM#616901",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:17:05.161619+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DPH1 were set to ",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:16:56.121033+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DPH1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:16:39.137357+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DPH1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25558065, 26220823; Phenotypes: Developmental delay with short stature, dysmorphic facial features, and sparse hair, MIM#616901; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPH1",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:47.528920+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DOK7 as ready",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:47.521722+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dok7 has been classified as Red List (Low Evidence).",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:40.684456+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DOK7 were changed from to Myasthenic syndrome, congenital, 10, MIM#254300",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:26.213850+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DOK7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:18.845518+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DOK7 as Red List (low evidence)",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:18.837352+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dok7 has been classified as Red List (Low Evidence).",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:08:02.831691+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DOK7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Myasthenic syndrome, congenital, 10, MIM#254300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DOK7",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:02:55.802567+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DOCK6 as ready",
"entity_name": "DOCK6",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:02:55.795012+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dock6 has been classified as Green List (High Evidence).",
"entity_name": "DOCK6",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:02:50.838983+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DOCK6 were changed from to Adams-Oliver syndrome 2, MIM#614219",
"entity_name": "DOCK6",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:02:33.258522+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DOCK6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DOCK6",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:02:18.568830+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DOCK6: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Adams-Oliver syndrome 2, MIM#614219; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DOCK6",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:00:41.003510+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DOCK4 as ready",
"entity_name": "DOCK4",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:00:40.996296+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dock4 has been classified as Red List (Low Evidence).",
"entity_name": "DOCK4",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:00:30.208401+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DOCK4 as Red List (low evidence)",
"entity_name": "DOCK4",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:00:30.201073+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dock4 has been classified as Red List (Low Evidence).",
"entity_name": "DOCK4",
"entity_type": "gene"
},
{
"created": "2019-12-01T17:00:16.516429+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DOCK4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DOCK4",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:55:15.411308+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNM1L as ready",
"entity_name": "DNM1L",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:55:15.403626+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnm1l has been classified as Green List (High Evidence).",
"entity_name": "DNM1L",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:55:03.740488+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.108",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNM1L were changed from to Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1, MIM#614388",
"entity_name": "DNM1L",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:54:47.475274+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.107",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DNM1L was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DNM1L",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:54:28.332853+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DNM1L: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1, MIM#614388; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "DNM1L",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:51:12.154338+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJC6 as ready",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:51:12.147126+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc6 has been classified as Red List (Low Evidence).",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:51:05.756857+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.106",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAJC6 were changed from to Parkinson disease 19a, juvenile-onset, MIM#615528",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:50:51.371278+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.105",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DNAJC6 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:50:40.222757+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJC6 as Red List (low evidence)",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:50:40.215175+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.104",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc6 has been classified as Red List (Low Evidence).",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T16:50:23.723864+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DNAJC6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Parkinson disease 19a, juvenile-onset, MIM#615528; Mode of inheritance: None",
"entity_name": "DNAJC6",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:18:25.320467+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJC12 as ready",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:18:25.311730+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc12 has been classified as Green List (High Evidence).",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:18:14.744656+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DNAJC12 were changed from to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:18:06.552733+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DNAJC12 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:15:44.857745+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJC12 as ready",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:15:44.850037+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc12 has been classified as Green List (High Evidence).",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:15:40.191874+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJC12 as Green List (high evidence)",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:15:40.184397+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.103",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc12 has been classified as Green List (High Evidence).",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:14:54.558522+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DNAJC12 was added\ngene: DNAJC12 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: DNAJC12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DNAJC12 were set to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384\nReview for gene: DNAJC12 was set to GREEN\nAdded comment: Highly variable neurological phenotype, including ID, dystonia, parkinsonism. Treatable. \nSources: Expert list",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:12:49.285716+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DNAJC12 as ready",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:12:49.278103+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc12 has been classified as Green List (High Evidence).",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:12:39.590310+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DNAJC12 as Green List (high evidence)",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:12:39.581849+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.6",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dnajc12 has been classified as Green List (High Evidence).",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:12:09.925266+11:00",
"panel_name": "Early onset Parkinson disease_MelbourneGenomics_VCGS",
"panel_id": 26,
"panel_version": "0.5",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: DNAJC12 was added\ngene: DNAJC12 was added to Early onset Parkinson disease_MelbourneGenomics_VCGS. Sources: Expert Review\nMode of inheritance for gene: DNAJC12 was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: DNAJC12 were set to Hyperphenylalaninemia, mild, non-BH4-deficient, MIM#617384\nReview for gene: DNAJC12 was set to GREEN\nAdded comment: Highly variable neurological phenotype, including ID, dystonia, parkinsonism. \nSources: Expert Review",
"entity_name": "DNAJC12",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:04:39.359528+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DMPK as ready",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:04:39.350368+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dmpk has been classified as Green List (High Evidence).",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:04:35.272938+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DMPK were changed from to Myotonic dystrophy 1, MIM#160900",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:04:25.249969+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.100",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DMPK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:04:09.189163+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DMPK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Myotonic dystrophy 1, MIM#160900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DMPK",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:01:27.666758+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLK1 as ready",
"entity_name": "DLK1",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:01:27.659275+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlk1 has been classified as Red List (Low Evidence).",
"entity_name": "DLK1",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:01:20.177634+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DLK1 as Red List (low evidence)",
"entity_name": "DLK1",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:01:20.169600+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.99",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlk1 has been classified as Red List (Low Evidence).",
"entity_name": "DLK1",
"entity_type": "gene"
},
{
"created": "2019-12-01T11:01:06.623887+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLK1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DLK1",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:55:54.932364+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLGAP2 as ready",
"entity_name": "DLGAP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:55:54.925420+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlgap2 has been classified as Red List (Low Evidence).",
"entity_name": "DLGAP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:55:48.601602+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DLGAP2 as Red List (low evidence)",
"entity_name": "DLGAP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:55:48.594395+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.98",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlgap2 has been classified as Red List (Low Evidence).",
"entity_name": "DLGAP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:55:35.730852+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLGAP2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DLGAP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:49:50.850594+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLG4 as ready",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:49:50.843527+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlg4 has been classified as Red List (Low Evidence).",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:49:41.827069+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DLG4 as Red List (low evidence)",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:49:41.819963+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlg4 has been classified as Red List (Low Evidence).",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:49:23.790372+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLG4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:48:56.451588+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLG4 as ready",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:48:56.444163+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlg4 has been classified as Red List (Low Evidence).",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:48:51.590679+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DLG4 as Red List (low evidence)",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:48:51.583150+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.97",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlg4 has been classified as Red List (Low Evidence).",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:48:37.776845+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLG4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "DLG4",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:42:22.032417+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLAT as ready",
"entity_name": "DLAT",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:42:22.018348+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dlat has been classified as Green List (High Evidence).",
"entity_name": "DLAT",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:42:15.809237+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLAT were changed from to Pyruvate dehydrogenase E2 deficiency, MIM#245348",
"entity_name": "DLAT",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:42:00.127590+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DLAT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DLAT",
"entity_type": "gene"
},
{
"created": "2019-12-01T10:41:44.698972+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLAT: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyruvate dehydrogenase E2 deficiency, MIM#245348; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DLAT",
"entity_type": "gene"
}
]
}