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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1075",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1073",
"results": [
{
"created": "2021-12-20T17:41:55.090261+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1539",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Marked gene: WNT10B as ready",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:41:55.080235+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1539",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: wnt10b has been classified as Green List (High Evidence).",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:41:36.163910+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1539",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Classified gene: WNT10B as Green List (high evidence)",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:41:36.152196+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1539",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: wnt10b has been classified as Green List (High Evidence).",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:41:09.487410+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1538",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "reviewed gene: WNT10B: Rating: GREEN; Mode of pathogenicity: None; Publications: 20635353, 24211389, 27321946; Phenotypes: Split-hand/foot malformation 6, OMIM #601906; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:36:09.592724+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Marked gene: WNT10B as ready",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:36:09.582190+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: wnt10b has been classified as Green List (High Evidence).",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:35:32.377025+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "reviewed gene: WNT10B: Rating: GREEN; Mode of pathogenicity: None; Publications: 20635353, 24211389, 27321946; Phenotypes: Split-hand/foot malformation 6, OMIM #601906, Tooth agenesis, selective, 8, OMIM #617073; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal",
"entity_name": "WNT10B",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:32:27.485265+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GABRB2 as ready",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:32:27.473568+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gabrb2 has been classified as Green List (High Evidence).",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:32:23.743989+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1538",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GANAB was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GANAB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:32:13.289639+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GANAB as Red List (low evidence)",
"entity_name": "GANAB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:32:13.278093+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1537",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ganab has been classified as Red List (Low Evidence).",
"entity_name": "GANAB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:31:58.582727+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GANAB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Polycystic kidney disease 3, MIM#600666; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GANAB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:30:45.961462+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1536",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: GABRB2 were changed from Epilepsy and intellectual disability to Developmental and epileptic encephalopathy 92 MIM#617829",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:30:12.999626+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1535",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: GABRB2 were set to ",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:30:01.693273+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1534",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of pathogenicity for gene: GABRB2 was changed from to Other",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:49.508688+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1533",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: GABRB2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:39.734670+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GABRB2 as Green List (high evidence)",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:39.724183+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1532",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gabrb2 has been classified as Green List (High Evidence).",
"entity_name": "GABRB2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:14.663943+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZNF699 as ready",
"entity_name": "ZNF699",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:14.652886+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf699 has been classified as Green List (High Evidence).",
"entity_name": "ZNF699",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:08.616257+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZNF699 as Green List (high evidence)",
"entity_name": "ZNF699",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:29:08.606397+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1531",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: znf699 has been classified as Green List (High Evidence).",
"entity_name": "ZNF699",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:37.457173+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ZMYM2 as ready",
"entity_name": "ZMYM2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:37.440416+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmym2 has been classified as Green List (High Evidence).",
"entity_name": "ZMYM2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:26.395432+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ZMYM2 as Green List (high evidence)",
"entity_name": "ZMYM2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:26.384718+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1530",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: zmym2 has been classified as Green List (High Evidence).",
"entity_name": "ZMYM2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:01.429649+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: UBR7 as ready",
"entity_name": "UBR7",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:28:01.420000+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ubr7 has been classified as Green List (High Evidence).",
"entity_name": "UBR7",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:55.785459+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: UBR7 as Green List (high evidence)",
"entity_name": "UBR7",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:55.774864+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1529",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ubr7 has been classified as Green List (High Evidence).",
"entity_name": "UBR7",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:44.617844+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.165",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: TLL1 were changed from to Atrial septal defect 6 MIM#613087",
"entity_name": "TLL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:26.052630+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TLL1 as ready",
"entity_name": "TLL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:26.040445+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tll1 has been classified as Green List (High Evidence).",
"entity_name": "TLL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:04.346364+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TLL1 as Green List (high evidence)",
"entity_name": "TLL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:27:04.335210+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1528",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tll1 has been classified as Green List (High Evidence).",
"entity_name": "TLL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:26:28.789679+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: TBX2 as ready",
"entity_name": "TBX2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:26:28.778915+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TBX2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:26:20.792163+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: TBX2 as Amber List (moderate evidence)",
"entity_name": "TBX2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:26:20.782035+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1527",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: tbx2 has been classified as Amber List (Moderate Evidence).",
"entity_name": "TBX2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:26:08.676802+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: TBX2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Vertebral anomalies and variable endocrine and T-cell dysfunction - MIM#618223; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "TBX2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:25:10.149265+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM58A as ready",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:25:10.139514+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam58a has been classified as Green List (High Evidence).",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:25:05.841326+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1526",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM58A were changed from STAR SYNDROME to STAR syndrome MIM#300707",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:53.765585+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1525",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FAM58A were set to ",
"entity_name": "FAM58A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:50.897340+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1524",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Marked gene: WRAP53 as ready",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:50.886767+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1524",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: wrap53 has been classified as Red List (Low Evidence).",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:40.037043+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1524",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Classified gene: WRAP53 as Red List (low evidence)",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:40.031962+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1524",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Added comment: Comment on list classification: Not suitable for fetal anomalies list",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:39.994999+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1524",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: wrap53 has been classified as Red List (Low Evidence).",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:22.879675+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: STK4 as ready",
"entity_name": "STK4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:22.869670+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stk4 has been classified as Green List (High Evidence).",
"entity_name": "STK4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:16.671378+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: STK4 as Green List (high evidence)",
"entity_name": "STK4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:24:16.661837+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1523",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: stk4 has been classified as Green List (High Evidence).",
"entity_name": "STK4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:43.272294+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPRED2 as ready",
"entity_name": "SPRED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:43.236444+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spred2 has been classified as Green List (High Evidence).",
"entity_name": "SPRED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:36.681096+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SPRED2 as Green List (high evidence)",
"entity_name": "SPRED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:36.671661+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1522",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spred2 has been classified as Green List (High Evidence).",
"entity_name": "SPRED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:10.761721+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SPEN as ready",
"entity_name": "SPEN",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:10.750372+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spen has been classified as Green List (High Evidence).",
"entity_name": "SPEN",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:03.728097+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SPEN as Green List (high evidence)",
"entity_name": "SPEN",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:23:03.713623+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1521",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: spen has been classified as Green List (High Evidence).",
"entity_name": "SPEN",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:22:34.956536+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: SMAD6 as ready",
"entity_name": "SMAD6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:22:34.938658+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smad6 has been classified as Green List (High Evidence).",
"entity_name": "SMAD6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:22:28.378271+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: SMAD6 as Green List (high evidence)",
"entity_name": "SMAD6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:22:28.368176+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1520",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: smad6 has been classified as Green List (High Evidence).",
"entity_name": "SMAD6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:21:42.657651+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM20C as ready",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:21:42.647792+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam20c has been classified as Green List (High Evidence).",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:21:38.883996+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1519",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM20C were changed from RAINE SYNDROME to Raine syndrome MIM#259775",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:21:27.054814+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1518",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FAM20C were set to ",
"entity_name": "FAM20C",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:20:46.747465+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: ROBO4 as ready",
"entity_name": "ROBO4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:20:46.735689+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: robo4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ROBO4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:20:39.395252+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: ROBO4 as Amber List (moderate evidence)",
"entity_name": "ROBO4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:20:39.384171+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1517",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: robo4 has been classified as Amber List (Moderate Evidence).",
"entity_name": "ROBO4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:20:26.554939+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: ROBO4: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "ROBO4",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:51.741695+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKACB as ready",
"entity_name": "PRKACB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:51.732217+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkacb has been classified as Green List (High Evidence).",
"entity_name": "PRKACB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:46.281318+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRKACB as Green List (high evidence)",
"entity_name": "PRKACB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:46.267696+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1516",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkacb has been classified as Green List (High Evidence).",
"entity_name": "PRKACB",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:23.750804+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRKACA as ready",
"entity_name": "PRKACA",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:23.740216+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkaca has been classified as Green List (High Evidence).",
"entity_name": "PRKACA",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:19.344149+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1515",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "reviewed gene: WRAP53: Rating: RED; Mode of pathogenicity: None; Publications: 21205863, 32303682, 29514627; Phenotypes: Dyskeratosis congenita, autosomal recessive 3, OMIM #613988; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "WRAP53",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:16.078219+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRKACA as Green List (high evidence)",
"entity_name": "PRKACA",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:18:16.064538+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1515",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prkaca has been classified as Green List (High Evidence).",
"entity_name": "PRKACA",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:43.746407+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM20A as ready",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:43.732951+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam20a has been classified as Red List (Low Evidence).",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:39.371496+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1514",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM20A were changed from AMELOGENESIS IMPERFECTA AND GINGIVAL FIBROMATOSIS SYNDROME to Amelogenesis imperfecta, type IG (enamel-renal syndrome) 204690",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:26.057522+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1513",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FAM20A were set to ",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:13.480025+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAM20A as Red List (low evidence)",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:17:13.466519+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1512",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam20a has been classified as Red List (Low Evidence).",
"entity_name": "FAM20A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:16:06.800841+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: FAM126A: Rating: GREEN; Mode of pathogenicity: None; Publications: 21911699, 17928815, 17683097, 16951682; Phenotypes: Leukodystrophy, hypomyelinating, 5 MIM#610532; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:15:51.352880+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: LINS1 as ready",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:15:51.343615+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: lins1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:15:45.793788+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1511",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: LINS1 were changed from AUTOSOMAL RECESSIVE MENTAL RETARDATION to Mental retardation, autosomal recessive 27 (MIM#614340); autosomal recessive intellectual disability (MIM#614340)",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:15:33.734617+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1510",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: LINS1 were set to ",
"entity_name": "LINS1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:14:12.694435+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PRDM6 as ready",
"entity_name": "PRDM6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:14:12.683242+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm6 has been classified as Red List (Low Evidence).",
"entity_name": "PRDM6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:14:04.850716+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: PRDM6 as Red List (low evidence)",
"entity_name": "PRDM6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:14:04.832065+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1509",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: prdm6 has been classified as Red List (Low Evidence).",
"entity_name": "PRDM6",
"entity_type": "gene"
}
]
}