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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=2078",
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"results": [
{
"created": "2019-12-01T21:08:05.055425+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.2",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eomes has been classified as Red List (Low Evidence).",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:07:47.695415+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:07:30.489689+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EOMES were set to ",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:07:13.367229+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EOMES as Red List (low evidence)",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:07:12.496335+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.1",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eomes has been classified as Red List (Low Evidence).",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:06:45.364457+11:00",
"panel_name": "Polymicrogyria and schizencephaly_AustralianGenomics_VCGS",
"panel_id": 18,
"panel_version": "0.0",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EOMES: Rating: RED; Mode of pathogenicity: None; Publications: 17353897; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:06:12.170518+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EOMES as ready",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:06:12.163296+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eomes has been classified as Red List (Low Evidence).",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:52.488643+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.167",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EOMES were changed from to Microcephaly",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:43.658220+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.166",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EOMES were set to ",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:33.115725+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EOMES was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:26.733204+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EOMES as Red List (low evidence)",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:26.725944+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.164",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eomes has been classified as Red List (Low Evidence).",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T21:05:14.285487+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EOMES: Rating: RED; Mode of pathogenicity: None; Publications: 17353897; Phenotypes: Microcephaly; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOMES",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:58.755113+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EOGT as ready",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:58.747254+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eogt has been classified as Red List (Low Evidence).",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:53.909697+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.163",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EOGT were changed from to Adams-Oliver syndrome 4, MIM#615297",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:36.982335+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.162",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EOGT were set to ",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:21.099335+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.161",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EOGT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:05.679273+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EOGT as Red List (low evidence)",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:57:05.671225+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.160",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eogt has been classified as Red List (Low Evidence).",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:56:53.206857+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EOGT: Rating: RED; Mode of pathogenicity: None; Publications: 31368252; Phenotypes: Adams-Oliver syndrome 4, MIM#615297; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EOGT",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:53:01.849336+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.159",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EIF2B5 were changed from to Leukoencephalopathy with vanishing white matter, MIM#603896",
"entity_name": "EIF2B5",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:52:53.824733+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.158",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF2B5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B5",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:52:42.598310+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EIF2B5 as Red List (low evidence)",
"entity_name": "EIF2B5",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:52:42.590825+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.157",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b5 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B5",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:52:13.034252+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EIF2B5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B5",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:59.551899+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EIF2B4 as ready",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:59.544673+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b4 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:55.433005+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.156",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EIF2B4 were changed from to Leukoencephalopathy with vanishing white matter, MIM#603896",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:43.319321+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.155",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF2B4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:31.892235+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EIF2B4 as Red List (low evidence)",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:31.884915+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.154",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b4 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:50:14.596729+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EIF2B4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B4",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:49:03.543907+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EIF2B3 as ready",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:49:03.535866+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b3 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:48:58.314397+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.153",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EIF2B3 were changed from to Leukoencephalopathy with vanishing white matter, MIM#603896",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:48:49.502489+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.152",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF2B3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:48:42.392080+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EIF2B3 as Red List (low evidence)",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:48:42.385010+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.151",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b3 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:48:29.222062+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EIF2B3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B3",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:47:22.226021+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EIF2B2 as ready",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:47:22.218227+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b2 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:47:17.794606+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.150",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EIF2B2 were changed from to Leukoencephalopathy with vanishing white matter, MIM#603896",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:47:06.192895+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.149",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF2B2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:46:55.343167+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EIF2B2 as Red List (low evidence)",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:46:55.336194+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.148",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b2 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:46:41.910072+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EIF2B2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:26.458536+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EIF2B1 as ready",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:26.450902+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b1 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:21.824171+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.147",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EIF2B1 were changed from to Leukoencephalopathy with vanishing white matter, MIM#603896",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:08.671225+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.146",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF2B1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:02.200326+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EIF2B1 as Red List (low evidence)",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:45:02.192674+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.145",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eif2b1 has been classified as Red List (Low Evidence).",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:44:50.183344+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EIF2B1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Leukoencephalopathy with vanishing white matter, MIM#603896; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EIF2B1",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:48.772343+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EFNB2 as ready",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:48.762871+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: efnb2 has been classified as Red List (Low Evidence).",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:43.514931+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.144",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EFNB2 were changed from to Intellectual disability and congenital abnormalities",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:31.816806+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.143",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EFNB2 were set to ",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:20.627278+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EFNB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:09.741621+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: EFNB2 as Red List (low evidence)",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:42:09.733156+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: efnb2 has been classified as Red List (Low Evidence).",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:41:49.278826+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EFNB2: Rating: RED; Mode of pathogenicity: None; Publications: 29508392; Phenotypes: Intellectual disability and congenital abnormalities; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EFNB2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:37:41.083600+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EDNRB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Waardenburg syndrome, type 4A, MIM#277580; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "EDNRB",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:33:18.189107+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EARS2 as ready",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:33:18.181009+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ears2 has been classified as Green List (High Evidence).",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:33:13.481300+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EARS2 were changed from to Combined oxidative phosphorylation deficiency 12, MIM#614924",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:32:57.281912+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EARS2 were set to ",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:32:44.556963+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.138",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:32:31.219944+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: EARS2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22492562; Phenotypes: Combined oxidative phosphorylation deficiency 12, MIM#614924; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EARS2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:54.669620+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CLIP2 as ready",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:54.662692+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clip2 has been classified as Red List (Low Evidence).",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:48.244112+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.137",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLIP2 were changed from Intellectual disability; SCA to Intellectual disability",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:34.416665+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.136",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: CLIP2 were changed from to Intellectual disability; SCA",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:20.535245+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.135",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CLIP2 were set to ",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:09.089079+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.134",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: CLIP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:02.721609+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CLIP2 as Red List (low evidence)",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T20:26:02.712457+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.133",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: clip2 has been classified as Red List (Low Evidence).",
"entity_name": "CLIP2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:16:13.985692+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DYNC2H1 as ready",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:16:13.978728+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dync2h1 has been classified as Red List (Low Evidence).",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:16:07.957932+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.132",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DYNC2H1 were changed from to Short-rib thoracic dysplasia 3 with or without polydactyly, MIM#613091",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:15:54.227379+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.131",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DYNC2H1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:15:46.706865+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DYNC2H1 as Red List (low evidence)",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:15:46.698924+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.130",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dync2h1 has been classified as Red List (Low Evidence).",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:15:33.842125+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DYNC2H1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Short-rib thoracic dysplasia 3 with or without polydactyly, MIM#613091; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DYNC2H1",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:09:50.844567+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DYM as ready",
"entity_name": "DYM",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:09:50.837004+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dym has been classified as Green List (High Evidence).",
"entity_name": "DYM",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:09:46.263187+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.129",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DYM were changed from to Dyggve-Melchior-Clausen disease, MIM#223800",
"entity_name": "DYM",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:09:32.449360+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.128",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DYM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DYM",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:09:15.290664+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DYM: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dyggve-Melchior-Clausen disease, MIM#223800; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DYM",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:07:14.311947+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DUOXA2 as ready",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:07:14.303464+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: duoxa2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:07:08.414789+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.127",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DUOXA2 were changed from to Thyroid dyshormonogenesis 5, MIM#274900",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:06:55.304705+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.126",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DUOXA2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:06:43.642339+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DUOXA2 as Amber List (moderate evidence)",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:06:43.635096+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.125",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: duoxa2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:06:29.620607+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DUOXA2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Thyroid dyshormonogenesis 5, MIM#274900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:03:43.596878+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSE as ready",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2019-12-01T18:03:43.588828+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.124",
"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": "2019-12-01T18:03:38.687026+11:00",
"panel_name": "Intellectual disability, syndromic and non-syndromic_GHQ",
"panel_id": 250,
"panel_version": "0.124",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DSE were changed from to Ehlers-Danlos syndrome, musculocontractural type 2, MIM#615539",
"entity_name": "DSE",
"entity_type": "gene"
}
]
}