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{
"count": 220324,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=827",
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"results": [
{
"created": "2022-05-20T16:17:57.765964+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AVPR2 as ready",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:17:57.754050+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avpr2 has been classified as Green List (High Evidence).",
"entity_name": "AVPR2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:17:32.555495+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14774",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DPY19L2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DPY19L2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:17:23.250848+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: AVP as ready",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:17:23.233712+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: avp has been classified as Green List (High Evidence).",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:46.953628+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14773",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: AVP were changed from to Diabetes insipidus, neurohypophyseal MIM#125700",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:46.534193+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DRAM2 as ready",
"entity_name": "DRAM2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:46.517099+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dram2 has been classified as Green List (High Evidence).",
"entity_name": "DRAM2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:36.767085+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14772",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DRAM2 were changed from to Cone-rod dystrophy 21 - MIM#616502",
"entity_name": "DRAM2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:16.412887+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14771",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: AVP were set to ",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:16:00.443016+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14770",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DRAM2 were set to ",
"entity_name": "DRAM2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:15:36.402582+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14769",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DRAM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DRAM2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:15:23.932942+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14768",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: AVP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "AVP",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:14:16.849700+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DRD2 as ready",
"entity_name": "DRD2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:14:16.836934+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: drd2 has been classified as Red List (Low Evidence).",
"entity_name": "DRD2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:14:03.573616+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP6V1E1 as ready",
"entity_name": "ATP6V1E1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:14:03.548648+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp6v1e1 has been classified as Green List (High Evidence).",
"entity_name": "ATP6V1E1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:13:55.354277+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14767",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP6V1E1 were changed from to Cutis laxa, autosomal recessive, type IIC MIM#617402",
"entity_name": "ATP6V1E1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:12:51.449244+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14766",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATP6V1E1 were set to ",
"entity_name": "ATP6V1E1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:12:35.216700+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DRD2 as Red List (low evidence)",
"entity_name": "DRD2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:12:35.193146+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14765",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: drd2 has been classified as Red List (Low Evidence).",
"entity_name": "DRD2",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:11:59.685316+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DRD3 as ready",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:11:59.672913+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: drd3 has been classified as Red List (Low Evidence).",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:11:55.750667+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14764",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP6V1E1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATP6V1E1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:11:41.804721+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14763",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DRD3 were changed from to {Essential tremor, hereditary, 1} - MIM#190300; {Schizophrenia, susceptibility to} - MIM#181500",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:11:03.867530+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14762",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DRD3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:10:44.034991+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DRD3 as Red List (low evidence)",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:10:44.021795+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14761",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: drd3 has been classified as Red List (Low Evidence).",
"entity_name": "DRD3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:10:40.937524+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ATP2A1 as ready",
"entity_name": "ATP2A1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:10:40.922746+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: atp2a1 has been classified as Green List (High Evidence).",
"entity_name": "ATP2A1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:10:14.061111+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14760",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ATP2A1 were changed from to Brody myopathy, OMIM # 601003",
"entity_name": "ATP2A1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:09:50.706170+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14759",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ATP2A1 were set to ",
"entity_name": "ATP2A1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:09:43.441107+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSC3 as ready",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:09:43.427466+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dsc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:09:34.037260+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14758",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DSC3 were changed from to Hypotrichosis and recurrent skin vesicles MIM#613102",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:09:24.821357+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14757",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ATP2A1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ATP2A1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:07:38.825357+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14756",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DSC3 were set to ",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:07:26.669109+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ADD1 as ready",
"entity_name": "ADD1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:07:26.652023+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: add1 has been classified as Green List (High Evidence).",
"entity_name": "ADD1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:07:20.271406+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DSC3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:07:08.444347+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14755",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ADD1 were changed from Intellectual disability, corpus callosum dysgenesis, and ventriculomegaly; no OMIM # to Neurodevelopmental disorder MONDO:0700092, ADD1-related",
"entity_name": "ADD1",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:04:57.338020+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DSC3 as Amber List (moderate evidence)",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:04:57.324014+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14754",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dsc3 has been classified as Amber List (Moderate Evidence).",
"entity_name": "DSC3",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:04:11.019932+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSCAM as ready",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:04:10.998408+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dscam has been classified as Green List (High Evidence).",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:04:00.871450+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14753",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DSCAM were changed from to Autism MONDO:0005260",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:03:17.267967+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14752",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DSCAM were set to ",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:02:55.938028+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DSCAM as Green List (high evidence)",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:02:55.926762+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14751",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dscam has been classified as Green List (High Evidence).",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:02:05.076210+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14750",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DSCAM was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:01:44.468520+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: DSCAM as Amber List (moderate evidence)",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:01:44.456746+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14749",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dscam has been classified as Amber List (Moderate Evidence).",
"entity_name": "DSCAM",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:00:47.784198+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSE as ready",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:00:47.768785+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14748",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dse has been classified as Green List (High Evidence).",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2022-05-20T16:00:39.531408+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14748",
"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"
},
{
"created": "2022-05-20T16:00:18.893998+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14747",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DSE were set to ",
"entity_name": "DSE",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:59:58.063197+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14746",
"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": "2022-05-20T15:59:00.932866+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSG4 as ready",
"entity_name": "DSG4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:59:00.920246+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dsg4 has been classified as Green List (High Evidence).",
"entity_name": "DSG4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:58:51.996136+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14745",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DSG4 were changed from to Hypotrichosis 6 - MIM#607903",
"entity_name": "DSG4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:58:32.389823+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14744",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DSG4 were set to ",
"entity_name": "DSG4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:58:11.089597+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14743",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DSG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DSG4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:57:30.721941+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DSPP as ready",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:57:30.707725+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dspp has been classified as Green List (High Evidence).",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:57:21.811931+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14742",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DSPP were changed from to Deafness, autosomal dominant 39, with dentinogenesis - MIM#605594; Dentin dysplasia, type II - MIM#125420; Dentinogenesis imperfecta, Shields type II - MIM#125490; Dentinogenesis imperfecta, Shields type III - MIM#125500",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:57:01.724459+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14741",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DSPP was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DSPP",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:56:21.590036+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DUOX2 as ready",
"entity_name": "DUOX2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:56:21.572142+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: duox2 has been classified as Green List (High Evidence).",
"entity_name": "DUOX2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:56:13.045655+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14740",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DUOX2 were changed from to Thyroid dyshormonogenesis 6 - MIM#607200",
"entity_name": "DUOX2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:55:52.363727+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14739",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DUOX2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "DUOX2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:44:55.918371+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14738",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Marked gene: GDNF as ready",
"entity_name": "GDNF",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:44:55.902756+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14738",
"user_name": "Elena Savva",
"item_type": "entity",
"text": "Gene: gdnf has been classified as Red List (Low Evidence).",
"entity_name": "GDNF",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:41:26.369804+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DUOXA2 as ready",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:41:26.355726+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14738",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: duoxa2 has been classified as Green List (High Evidence).",
"entity_name": "DUOXA2",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:41:17.600260+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14738",
"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": "2022-05-20T15:40:55.773196+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14737",
"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": "2022-05-20T15:39:54.470398+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ENPP1 as ready",
"entity_name": "ENPP1",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:39:54.457112+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: enpp1 has been classified as Green List (High Evidence).",
"entity_name": "ENPP1",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:39:20.437195+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPOR as ready",
"entity_name": "EPOR",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:39:20.424510+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: epor has been classified as Green List (High Evidence).",
"entity_name": "EPOR",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:38:36.927177+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPRS as ready",
"entity_name": "EPRS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:38:36.915133+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eprs has been classified as Green List (High Evidence).",
"entity_name": "EPRS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:38:04.705167+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EPS8 as ready",
"entity_name": "EPS8",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:38:04.690128+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eps8 has been classified as Green List (High Evidence).",
"entity_name": "EPS8",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:37:55.970618+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14736",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EPS8 were changed from to Autosomal recessive nonsyndromic hearing loss 102 MONDO:0014428",
"entity_name": "EPS8",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:35:31.896521+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14735",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EPS8 were set to ",
"entity_name": "EPS8",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:35:11.686854+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14734",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EPS8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EPS8",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:34:20.665963+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ETFB as ready",
"entity_name": "ETFB",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:34:20.652577+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: etfb has been classified as Green List (High Evidence).",
"entity_name": "ETFB",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:34:11.019073+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14733",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ETFB were changed from to multiple acyl-CoA dehydrogenase deficiency MONDO:0009282",
"entity_name": "ETFB",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:33:23.782940+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EXT1 as ready",
"entity_name": "EXT1",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:33:23.769541+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ext1 has been classified as Green List (High Evidence).",
"entity_name": "EXT1",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:33:10.894985+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14732",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EXT1 were changed from to hereditary multiple osteochondromas MONDO:0005508; exostoses, multiple, type 1 MONDO:0007585",
"entity_name": "EXT1",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:32:27.373786+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EYA4 as ready",
"entity_name": "EYA4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:32:27.360861+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eya4 has been classified as Green List (High Evidence).",
"entity_name": "EYA4",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:31:45.627443+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: EYS as ready",
"entity_name": "EYS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:31:45.612108+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: eys has been classified as Green List (High Evidence).",
"entity_name": "EYS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:31:33.610055+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14731",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: EYS were changed from to Retinitis pigmentosa 25 MONDO:0011272",
"entity_name": "EYS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:31:10.604661+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14730",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: EYS were set to ",
"entity_name": "EYS",
"entity_type": "gene"
},
{
"created": "2022-05-20T15:30:35.367824+10:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.14729",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: EYS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "EYS",
"entity_type": "gene"
}
]
}