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{
"count": 220363,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1479",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1477",
"results": [
{
"created": "2020-12-11T15:27:36.809753+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WEE2 as ready",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:27:36.799132+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wee2 has been classified as Green List (High Evidence).",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:27:18.162932+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TUBB8 as ready",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:27:18.152723+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tubb8 has been classified as Red List (Low Evidence).",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:27:15.917184+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.116",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TUBB8 were changed from to Oocyte maturation defect 2, MIM# 616780",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:27:06.607092+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.115",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: TUBB8 were set to ",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:26:57.767104+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.114",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: TUBB8 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:26:47.541919+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.113",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TUBB8: Rating: RED; Mode of pathogenicity: None; Publications: 26789871, 27273344; Phenotypes: Oocyte maturation defect 2, MIM# 616780; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "TUBB8",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:24:48.824232+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5619",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WEE2 were changed from to Oocyte maturation defect 5, MIM# 617996",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:23:23.838238+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.113",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: MRPS22 as ready",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:23:23.827852+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.113",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: mrps22 has been classified as Green List (High Evidence).",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:23:20.072245+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.113",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: MRPS22 as Green List (high evidence)",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:23:20.063404+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.113",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: mrps22 has been classified as Green List (High Evidence).",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:23:11.167884+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.112",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: MRPS22: Rating: GREEN; Mode of pathogenicity: None; Publications: 29566152, 31042289; Phenotypes: Ovarian dysgenesis 7 MIM#618117; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:20:10.319228+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5618",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WEE2 were set to ",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:19:37.324013+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5617",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WEE2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:19:19.537675+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WEE2: Rating: GREEN; Mode of pathogenicity: None; Publications: 29606300, 30628060; Phenotypes: Oocyte maturation defect 5, MIM# 617996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:19:17.526185+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.112",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Deleted their review",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:28.304082+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: WEE2 as ready",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:28.292896+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: wee2 has been classified as Red List (Low Evidence).",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:25.912022+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.112",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: WEE2 were changed from to Oocyte maturation defect 5, MIM# 617996",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:18.411000+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.111",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: WEE2 were set to ",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:10.895108+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.110",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: WEE2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:18:01.616094+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.109",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: WEE2: Rating: RED; Mode of pathogenicity: None; Publications: 29606300, 30628060; Phenotypes: Oocyte maturation defect 5, MIM# 617996; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "WEE2",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:02:58.923701+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.109",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: MRPS22: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: Ovarian dysgenesis 7 618117; Mode of inheritance: None",
"entity_name": "MRPS22",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:43.344462+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.109",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: EIF4ENIF1 were changed from to Primary ovarian insufficiency",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:35.037284+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.108",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: EIF4ENIF1 were set to ",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:27.911593+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.107",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: EIF4ENIF1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:18.505015+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.106",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: EIF4ENIF1 as Amber List (moderate evidence)",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:18.494238+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.106",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: eif4enif1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T15:00:08.167827+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.105",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: EIF4ENIF1: Rating: AMBER; Mode of pathogenicity: None; Publications: 31810472, 23902945, 33095795; Phenotypes: Primary ovarian insufficiency; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "EIF4ENIF1",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:21:50.523852+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.105",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: DACH2 were changed from to Primary ovarian insufficiency",
"entity_name": "DACH2",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:21:43.059760+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.104",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: DACH2 were set to ",
"entity_name": "DACH2",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:21:34.398264+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.103",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: DACH2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DACH2",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:21:15.058315+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: DACH2: Rating: RED; Mode of pathogenicity: None; Publications: 15459172; Phenotypes: Primary ovarian insufficiency; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DACH2",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:00:25.093600+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: HNF1B as ready",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2020-12-11T14:00:25.080980+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: hnf1b has been classified as Red List (Low Evidence).",
"entity_name": "HNF1B",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:36.862477+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: GDF9 as ready",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:36.851484+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gdf9 has been classified as Green List (High Evidence).",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:32.678972+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.102",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: GDF9 were set to 29044499; 8849725",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:23.689921+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.101",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: GDF9 as Green List (high evidence)",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:23.677417+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.101",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: gdf9 has been classified as Green List (High Evidence).",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:55:05.024999+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.100",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "edited their review of gene: GDF9: Added comment: PMID: 33036707 - Additional compound het case with primary amenorrhea and was diagnosed with non-syndromic POI and supporting functional assays.; Changed rating: GREEN; Changed publications: 29044499, 8849725, 33036707",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:49:11.085974+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.100",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: FANCM as ready",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:49:11.052602+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.100",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: fancm has been classified as Green List (High Evidence).",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:49:07.785833+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.100",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: FANCM were changed from to Premature ovarian failure 15 MIM#618096",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:47:59.155280+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.99",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: FANCM were set to ",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:47:28.541080+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.98",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: FANCM was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:47:17.011628+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.97",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: FANCM as Green List (high evidence)",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:47:16.999447+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.97",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: fancm has been classified as Green List (High Evidence).",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:46:42.655160+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.96",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "reviewed gene: FANCM: Rating: GREEN; Mode of pathogenicity: None; Publications: 29231814, 28837162, 33036707, 25010009; Phenotypes: Premature ovarian failure 15 MIM#618096; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FANCM",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:02:42.165603+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZP1 as ready",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:02:42.154185+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp1 has been classified as Green List (High Evidence).",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:02:32.642032+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZP1 as Green List (high evidence)",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:02:32.634378+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5616",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp1 has been classified as Green List (High Evidence).",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:02:01.209410+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5615",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZP1 was added\ngene: ZP1 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: ZP1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: ZP1 were set to 24670168; 30810869; 32573113; 33272616\nPhenotypes for gene: ZP1 were set to Oocyte maturation defect 1, MIM# 615774\nReview for gene: ZP1 was set to GREEN\nAdded comment: Multiple unrelated individuals reported, presents as primary infertility. \nSources: Expert list",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:00:06.195298+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZP1 as ready",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:00:06.183718+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp1 has been classified as Red List (Low Evidence).",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T13:00:03.706922+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.96",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZP1 were changed from to Oocyte maturation defect 1, MIM# 615774",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:59:55.100918+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.95",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZP1 were set to ",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:59:45.580017+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.94",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZP1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:59:34.924880+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZP1: Rating: RED; Mode of pathogenicity: None; Publications: 24670168, 30810869, 32573113, 33272616; Phenotypes: Oocyte maturation defect 1, MIM# 615774; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "ZP1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:56:15.824873+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5614",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZP2 were changed from Female infertility to Oocyte maturation defect 6, MIM# 618353; Female infertility",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:55:56.372321+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ZP2: Changed phenotypes: Oocyte maturation defect 6, MIM# 618353, Female infertility",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:55:17.643932+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZP2 as ready",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:55:17.634342+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp2 has been classified as Red List (Low Evidence).",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:55:14.267478+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.93",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZP2 were changed from to Oocyte maturation defect 6, MIM#\t618353; Female infertility",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:54:51.368947+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.92",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZP2 were set to ",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:54:42.535779+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.91",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:54:32.558707+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: Three unrelated individuals reported with bi-allelic variants in this gene and thin zona pellucida. \nSources: Literature; to: Three unrelated individuals reported with bi-allelic variants in this gene and thin zona pellucida. Presents with primary infertility rather than POI/POF.\r\nSources: Literature",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:54:13.832863+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: ZP2: Changed rating: RED",
"entity_name": "ZP2",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:53:31.680332+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZP3 as ready",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:53:31.668057+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp3 has been classified as Green List (High Evidence).",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:53:21.704861+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZP3 as Green List (high evidence)",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:53:21.696118+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5613",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp3 has been classified as Green List (High Evidence).",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:53:04.091293+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.5612",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "gene: ZP3 was added\ngene: ZP3 was added to Mendeliome. Sources: Expert list\nMode of inheritance for gene: ZP3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: ZP3 were set to 28886344; 30810869; 33272616; 32573113\nPhenotypes for gene: ZP3 were set to Oocyte maturation defect 3, MIM# 617712\nReview for gene: ZP3 was set to GREEN\nAdded comment: Oocyte maturation defect with normal ovarian reserves and menstrual cycles, presents as infertility. \nSources: Expert list",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:43:31.070138+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZP3 as ready",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:43:31.045757+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zp3 has been classified as Red List (Low Evidence).",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:43:28.501412+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.90",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: ZP3 were changed from to Oocyte maturation defect 3, MIM# 617712",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:43:19.806711+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.89",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: ZP3 were set to ",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:43:07.059002+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.88",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: ZP3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:42:55.613810+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.87",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ZP3: Rating: RED; Mode of pathogenicity: None; Publications: 28886344, 30810869; Phenotypes: Oocyte maturation defect 3, MIM# 617712; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "ZP3",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:45.915115+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.87",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: ERAL1 as ready",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:45.904519+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.87",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: eral1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:40.665964+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.87",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: ERAL1 were changed from to Perrault syndrome 6, MIM# 617565",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:33.187305+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.86",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: ERAL1 were set to ",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:24.090791+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.85",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: ERAL1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:17.816376+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.84",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: ERAL1 as Amber List (moderate evidence)",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:34:17.805462+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.84",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: eral1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ERAL1",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:33:10.611042+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.83",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: BTG4 as ready",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:33:10.603417+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.83",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: btg4 has been classified as Green List (High Evidence).",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:33:07.648691+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.83",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: BTG4 were set to ",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:33:01.534127+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.82",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: BTG4 were changed from to Oocyte maturation defect, MIM#619009",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:32:51.435839+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.81",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: BTG4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:32:44.181771+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.80",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Classified gene: BTG4 as Green List (high evidence)",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:32:44.170261+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.80",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Gene: btg4 has been classified as Green List (High Evidence).",
"entity_name": "BTG4",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:31:54.846660+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.79",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Phenotypes for gene: GDF9 were changed from to Premature ovarian failure 14 MIM#618014",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:31:46.101876+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.78",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Publications for gene: GDF9 were set to ",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:31:36.603913+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.77",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Mode of inheritance for gene: GDF9 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GDF9",
"entity_type": "gene"
},
{
"created": "2020-12-11T12:31:10.906098+11:00",
"panel_name": "Primary Ovarian Insufficiency_Premature Ovarian Failure",
"panel_id": 3166,
"panel_version": "0.76",
"user_name": "Bryony Thompson",
"item_type": "entity",
"text": "Marked gene: FEZF1 as ready",
"entity_name": "FEZF1",
"entity_type": "gene"
}
]
}