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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2062",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2060",
"results": [
{
"created": "2019-12-07T18:10:55.202188+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.818",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndn has been classified as Red List (Low Evidence).",
"entity_name": "NDN",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:10:43.671917+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NDN: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "NDN",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:08:17.733170+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NAGS as ready",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:08:17.725693+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nags has been classified as Red List (Low Evidence).",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:08:08.051510+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.817",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NAGS were changed from to N-acetylglutamate synthase deficiency, MIM#237310",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:07:58.931234+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.816",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: NAGS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:07:51.985689+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NAGS as Red List (low evidence)",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:07:51.976903+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.815",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nags has been classified as Red List (Low Evidence).",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:07:39.295717+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NAGS: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: N-acetylglutamate synthase deficiency, MIM#237310; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NAGS",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:03:28.910971+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS16 as ready",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:03:28.903729+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:03:25.198690+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.36",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPS16 were changed from to Combined oxidative phosphorylation deficiency 2; OMIM #610498",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:03:03.318536+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.35",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRPS16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:02:41.522795+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.34",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPS16 were set to ",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:02:20.217464+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS16 as Amber List (moderate evidence)",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T18:02:20.208755+11:00",
"panel_name": "Callosome_VCGS",
"panel_id": 205,
"panel_version": "0.33",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:52.990834+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS16 as ready",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:52.982898+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:52.741933+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS16 as ready",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:52.733732+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:45.441115+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.182",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPS16 were changed from to Combined oxidative phosphorylation deficiency 2; OMIM #610498",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:32.086240+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.181",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPS16 were set to ",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:59:10.319727+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.180",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRPS16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:58:54.621555+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS16 as Amber List (moderate evidence)",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:58:54.610871+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.179",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:53.346967+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPS16 as ready",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:53.338698+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:52.903693+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS16 as Amber List (moderate evidence)",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:52.898355+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Amber for mitochondrial.",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:52.875429+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:35.624228+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.23",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPS16 were changed from to Combined oxidative phosphorylation deficiency 2; OMIM #610498",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:18.471354+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPS16 were set to ",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:54:01.919372+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRPS16 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:53:45.579282+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPS16 as Amber List (moderate evidence)",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:53:45.566099+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Amber for mitochondrial.",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:53:45.355527+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.22",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrps16 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPS16",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:40:14.785733+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPL3 as ready",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:40:14.778341+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrpl3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:40:07.173631+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.177",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPL3 were changed from to Combined oxidative phosphorylation deficiency 9; OMIM #614582",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:39:52.706533+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.176",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPL3 were set to ",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:39:37.547201+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.175",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRPL3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:39:24.227007+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPL3 as Amber List (moderate evidence)",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:39:24.219088+11:00",
"panel_name": "Mendeliome_VCGS",
"panel_id": 137,
"panel_version": "0.174",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrpl3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:33:20.256242+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MRPL3 as ready",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:33:20.247657+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrpl3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:33:17.161084+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.19",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MRPL3 were changed from to Combined oxidative phosphorylation deficiency 9; OMIM #614582",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:32:57.209755+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.18",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MRPL3 were set to ",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:32:36.517076+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.17",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: MRPL3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:32:11.207491+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MRPL3 as Amber List (moderate evidence)",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:32:11.193169+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.16",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mrpl3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T17:31:44.464460+11:00",
"panel_name": "Mitochondrial_AustralianGenomics_VCGS",
"panel_id": 203,
"panel_version": "0.15",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: MRPL3: Rating: AMBER; Mode of pathogenicity: None; Publications: 27815843, 21786366; Phenotypes: Combined oxidative phosphorylation deficiency 9, OMIM #614582; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPL3",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:36:32.753547+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLCN2 as ready",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:36:32.745842+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:36:26.732930+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.814",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLCN2 were changed from to Leukoencephalopathy with ataxia, MIM#615651",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:36:18.326639+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.813",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLCN2 were set to ",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:36:09.589625+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.812",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLCN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:58.874497+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLCN2 as Amber List (moderate evidence)",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:58.866319+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.811",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clcn2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CLCN2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:36.925817+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CISD2 as ready",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:36.918542+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cisd2 has been classified as Red List (Low Evidence).",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:32.439079+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.810",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CISD2 were changed from to Wolfram syndrome 2, MIM#604928",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:21.912189+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.809",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CISD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:15.459948+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CISD2 as Red List (low evidence)",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:35:15.452117+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.808",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cisd2 has been classified as Red List (Low Evidence).",
"entity_name": "CISD2",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:48.644855+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CHST14 as ready",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:48.637868+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chst14 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:43.795807+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.807",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CHST14 were changed from to Ehlers-Danlos syndrome, musculocontractural type 1, MIM#601776",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:28.947712+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.806",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CHST14 were set to ",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:19.382665+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.805",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CHST14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:13.292654+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CHST14 as Amber List (moderate evidence)",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:34:13.284092+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.804",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: chst14 has been classified as Amber List (Moderate Evidence).",
"entity_name": "CHST14",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:33:40.149137+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CACNA1E as ready",
"entity_name": "CACNA1E",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:33:40.142210+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1e has been classified as Green List (High Evidence).",
"entity_name": "CACNA1E",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:33:34.610752+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CACNA1E as Green List (high evidence)",
"entity_name": "CACNA1E",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:33:34.600463+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.803",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cacna1e has been classified as Green List (High Evidence).",
"entity_name": "CACNA1E",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:59.160632+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATAD1 as ready",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:59.153685+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad1 has been classified as Green List (High Evidence).",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:53.847962+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ATAD1 as Green List (high evidence)",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:53.840171+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.802",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atad1 has been classified as Green List (High Evidence).",
"entity_name": "ATAD1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:18.453390+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ASTN1 as ready",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:18.446467+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: astn1 has been classified as Green List (High Evidence).",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:12.269174+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ASTN1 as Green List (high evidence)",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:32:12.262173+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.801",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: astn1 has been classified as Green List (High Evidence).",
"entity_name": "ASTN1",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:31:47.122294+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ASH1L as ready",
"entity_name": "ASH1L",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:31:47.115178+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ash1l has been classified as Green List (High Evidence).",
"entity_name": "ASH1L",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:31:41.393066+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ASH1L as Green List (high evidence)",
"entity_name": "ASH1L",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:31:41.383780+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.800",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ash1l has been classified as Green List (High Evidence).",
"entity_name": "ASH1L",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:25:25.732810+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AGO3 as ready",
"entity_name": "AGO3",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:25:25.725450+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ago3 has been classified as Red List (Low Evidence).",
"entity_name": "AGO3",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:25:16.790477+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.799",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: AGO3 was added\ngene: AGO3 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: AGO3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: AGO3 were set to 25271087\nPhenotypes for gene: AGO3 were set to Intellectual disability\nReview for gene: AGO3 was set to RED\nAdded comment: Five children with heterozygous deletions of AGO3 reported; however deletions also encompass AGO1 and therefore gene-disease association cannot be firmly established until SNVs reported/functional data becomes available. \nSources: Expert list",
"entity_name": "AGO3",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:21:47.386223+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADRA2B as ready",
"entity_name": "ADRA2B",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:21:47.379004+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: adra2b has been classified as Red List (Low Evidence).",
"entity_name": "ADRA2B",
"entity_type": "gene"
},
{
"created": "2019-12-07T13:21:37.926979+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.798",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ADRA2B was added\ngene: ADRA2B was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert list\nMode of inheritance for gene: ADRA2B was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ADRA2B were set to 24114805; 21937992\nPhenotypes for gene: ADRA2B were set to Cortical myoclonus and epilepsy; Intellectual disability\nReview for gene: ADRA2B was set to RED\nAdded comment: Two families reported but same mutation, ?founder effect. Most affected individuals had normal intellect.\r\nAnother paper linking to AR intellectual disability but as part of manuscript reporting multiple novel candidates. \nSources: Expert list",
"entity_name": "ADRA2B",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:39:09.735238+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CFHR3 as ready",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:39:09.728164+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfhr3 has been classified as Red List (Low Evidence).",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:39:03.354730+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.797",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CFHR3 were changed from to Hemolytic uremic syndrome, atypical, susceptibility to, MIM#235400",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:38:50.486874+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.796",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CFHR3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:38:43.361691+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.795",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CFHR3 as Red List (low evidence)",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:38:43.354634+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.795",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cfhr3 has been classified as Red List (Low Evidence).",
"entity_name": "CFHR3",
"entity_type": "gene"
},
{
"created": "2019-12-07T11:38:16.700872+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": "Marked gene: CFHR1 as ready",
"entity_name": "CFHR1",
"entity_type": "gene"
}
]
}