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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1076",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1074",
"results": [
{
"created": "2021-12-20T17:13:51.341874+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PRDM6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Patent ductus arteriosus 3 - MIM#617039; Mode of inheritance: None",
"entity_name": "PRDM6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:12:56.043128+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAM126A as ready",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:12:56.020795+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fam126a has been classified as Green List (High Evidence).",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:12:40.542290+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1508",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAM126A were changed from LEUKODYSTROPHY HYPOMYELINATING TYPE 5 to Leukodystrophy, hypomyelinating, 5 MIM#610532",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:12:28.192205+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1507",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FAM126A were set to ",
"entity_name": "FAM126A",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:11:02.084882+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NKX2-6 as ready",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:11:02.073687+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nkx2-6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:10:56.874905+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1506",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NKX2-6 were changed from to Conotruncal heart malformations - MIM#217095; Persistent truncus arteriosus - MIM#217095",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:10:42.601175+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1505",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: NKX2-6 as Amber List (moderate evidence)",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:10:42.590048+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1505",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nkx2-6 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:10:30.214999+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: NKX2-6: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Conotruncal heart malformations - MIM#217095, Persistent truncus arteriosus - MIM#217095; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "NKX2-6",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:09:29.886790+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT74 as ready",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:09:29.876673+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Red List (Low Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:09:25.949895+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1504",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT74 were changed from HYPOTRICHOSIS SIMPLEX OF THE SCALP 2 to Woolly hair, autosomal dominant (MIM#194300)",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:09:13.523840+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1503",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: KRT74 were set to ",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:09:02.449258+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1502",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KRT74 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:51.399295+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KRT74 as Red List (low evidence)",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:51.388188+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1501",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt74 has been classified as Red List (Low Evidence).",
"entity_name": "KRT74",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:19.951714+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FAH as ready",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:19.935916+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fah has been classified as Red List (Low Evidence).",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:14.285583+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1500",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Marked gene: YY1 as ready",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:14.273297+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1500",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Gene: yy1 has been classified as Green List (High Evidence).",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:13.442110+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1500",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: FAH were changed from TYROSINEMIA TYPE 1 to Tyrosinemia, type I, MIM#276700",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:00.747809+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1499",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: FAH were set to ",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:08:00.178509+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1499",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Phenotypes for gene: YY1 were changed from INTELLECTUAL DISABILITY to Gabriele-de Vries syndrome, OMIM #617557",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:07:47.771811+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FAH as Red List (low evidence)",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:07:47.759617+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1498",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fah has been classified as Red List (Low Evidence).",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:07:38.540103+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1497",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "Mode of inheritance for gene: YY1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:07:36.625064+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FAH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Tyrosinemia, type I, MIM#276700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "FAH",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:06:28.137489+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "reviewed gene: YY1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575647; Phenotypes: Gabriele-de Vries syndrome, OMIM #617557; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:05:14.907226+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MYBPC3 as ready",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:05:14.896203+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mybpc3 has been classified as Green List (High Evidence).",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:05:07.765515+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MYBPC3 as Green List (high evidence)",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:05:07.754675+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1496",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mybpc3 has been classified as Green List (High Evidence).",
"entity_name": "MYBPC3",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:04:11.054766+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KCNJ8 as ready",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:04:11.044309+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Green List (High Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:04:03.144798+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1495",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: KCNJ8 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:03:20.656960+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Alison Yeung",
"item_type": "entity",
"text": "reviewed gene: YY1: Rating: GREEN; Mode of pathogenicity: None; Publications: 28575647; Phenotypes: Gabriele-de Vries syndrome, OMIM #617557; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "YY1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:02:33.011455+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: KCNJ8 as Green List (high evidence)",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:02:32.993987+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1494",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: kcnj8 has been classified as Green List (High Evidence).",
"entity_name": "KCNJ8",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:58.548777+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMP15 as ready",
"entity_name": "MMP15",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:58.537662+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmp15 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MMP15",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:51.700906+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MMP15 as Amber List (moderate evidence)",
"entity_name": "MMP15",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:51.691108+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1493",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmp15 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MMP15",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:21.087718+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MIB1 as ready",
"entity_name": "MIB1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:21.077422+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mib1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MIB1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:14.037788+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MIB1 as Amber List (moderate evidence)",
"entity_name": "MIB1",
"entity_type": "gene"
},
{
"created": "2021-12-20T17:00:14.023937+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1492",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mib1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MIB1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:59:39.307995+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MESP1 as ready",
"entity_name": "MESP1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:59:39.289014+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mesp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MESP1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:59:33.300233+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: MESP1 as Amber List (moderate evidence)",
"entity_name": "MESP1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:59:33.290681+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1491",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mesp1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "MESP1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:58:38.398677+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: HSPA9 as ready",
"entity_name": "HSPA9",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:58:38.388832+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspa9 has been classified as Green List (High Evidence).",
"entity_name": "HSPA9",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:58:29.264090+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: HSPA9 as Green List (high evidence)",
"entity_name": "HSPA9",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:58:29.252130+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1490",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: hspa9 has been classified as Green List (High Evidence).",
"entity_name": "HSPA9",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:54:12.371219+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GM2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 28417072, 28192816, 27402091; Phenotypes: GM2-gangliosidosis, AB variant MIM#272750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GM2A",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:53:49.446651+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: FOXH1: Rating: RED; Mode of pathogenicity: None; Publications: 32003456; Phenotypes: Congenital heart disease; Mode of inheritance: None",
"entity_name": "FOXH1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:52:18.887270+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GM2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 28417072, 28192816, 27402091, 33819415; Phenotypes: GM2-gangliosidosis, AB variant MIM#272750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GM2A",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:41.283045+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: FBRSL1 as ready",
"entity_name": "FBRSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:41.272515+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbrsl1 has been classified as Green List (High Evidence).",
"entity_name": "FBRSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:34.284959+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: FBRSL1 as Green List (high evidence)",
"entity_name": "FBRSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:34.272614+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1489",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: fbrsl1 has been classified as Green List (High Evidence).",
"entity_name": "FBRSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:03.431773+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OSTM1 as ready",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:45:03.409000+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ostm1 has been classified as Green List (High Evidence).",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:44:18.577586+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: CITED2 as ready",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:44:18.568364+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cited2 has been classified as Green List (High Evidence).",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:44:12.773869+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1488",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: CITED2 were set to 11694877; 16287139",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:43:58.020354+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: CITED2 as Green List (high evidence)",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:43:58.009995+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1487",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: cited2 has been classified as Green List (High Evidence).",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:43:37.721725+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: CITED2: Rating: GREEN; Mode of pathogenicity: None; Publications: 33706167, 33439552, 31515672, 29536580; Phenotypes: Atrial septal defect 8 - MIM#614433, Ventricular septal defect 2 - MIM#614431; Mode of inheritance: None",
"entity_name": "CITED2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:40:19.179748+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BMPR2 as ready",
"entity_name": "BMPR2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:40:19.169364+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bmpr2 has been classified as Red List (Low Evidence).",
"entity_name": "BMPR2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:40:11.103403+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BMPR2 as Red List (low evidence)",
"entity_name": "BMPR2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:40:11.091975+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1486",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bmpr2 has been classified as Red List (Low Evidence).",
"entity_name": "BMPR2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:39:56.975226+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BMPR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None",
"entity_name": "BMPR2",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:38:44.845806+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OPHN1 as ready",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:38:44.834968+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ophn1 has been classified as Green List (High Evidence).",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:38:44.365522+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1485",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OSTM1 were changed from Osteopetrosis 259720 to Osteopetrosis, autosomal recessive 5 (MIM#259720)",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:38:32.592621+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1484",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OSTM1 were set to ",
"entity_name": "OSTM1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:37:54.738742+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OCLN as ready",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:37:54.728920+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ocln has been classified as Green List (High Evidence).",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:37:52.540642+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1483",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OPHN1 were changed from Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance, 300486 to Intellectual developmental disorder, X-linked syndromic, Billuart type (MIM#300486)",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:37:38.863851+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1482",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OPHN1 were set to ",
"entity_name": "OPHN1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:55.902708+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: OBSL1 as ready",
"entity_name": "OBSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:55.887098+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: obsl1 has been classified as Green List (High Evidence).",
"entity_name": "OBSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:53.887945+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1481",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OCLN were changed from Band-like calcification with simplified gyration and polymicrogyria 251290 to Pseudo-TORCH syndrome 1 (MIM#251290)",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:40.181579+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1480",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OCLN were set to ",
"entity_name": "OCLN",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:09.947110+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1479",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: OBSL1 were changed from 3-M SYNDROME 2 to 3-M syndrome 2 (MIM#612921)",
"entity_name": "OBSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:01.538837+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.243",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "gene: GLI1 was added\ngene: GLI1 was added to Polydactyly. Sources: Literature\nMode of inheritance for gene: GLI1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GLI1 were set to 34721536; 31621941; 31549748; 30620395\nPhenotypes for gene: GLI1 were set to Polydactyly, postaxial, type A8 MIM#618123; Polydactyly, preaxial I MIM#174400\nPenetrance for gene: GLI1 were set to unknown\nReview for gene: GLI1 was set to GREEN\ngene: GLI1 was marked as current diagnostic\nAdded comment: >10 unrelated probands reported, both AD and AR reported \nSources: Literature",
"entity_name": "GLI1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:36:00.925987+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1478",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: OBSL1 were set to ",
"entity_name": "OBSL1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:18.158690+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NR0B1 as ready",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:18.144236+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nr0b1 has been classified as Amber List (Moderate Evidence).",
"entity_name": "NR0B1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:17.943969+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "reviewed gene: GLI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 34721536, 31621941, 31549748, 30620395; Phenotypes: Polydactyly, postaxial, type A8 MIM#618123, Polydactyly, preaxial I MIM#174400; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes",
"entity_name": "GLI1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:14.838181+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NUBPL as ready",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:14.809153+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nubpl has been classified as Green List (High Evidence).",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:13.804074+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.10312",
"user_name": "Ain Roesley",
"item_type": "entity",
"text": "gene: GLI1 was added\ngene: GLI1 was added to Mendeliome. Sources: Literature\nMode of inheritance for gene: GLI1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal\nPublications for gene: GLI1 were set to 34721536; 31621941; 31549748; 30620395\nPhenotypes for gene: GLI1 were set to Polydactyly, postaxial, type A8\tMIM#618123; Polydactyly, preaxial I\tMIM#174400\nPenetrance for gene: GLI1 were set to unknown\nReview for gene: GLI1 was set to GREEN\ngene: GLI1 was marked as current diagnostic\nAdded comment: >10 unrelated probands reported, both AD and AR reported \nSources: Literature",
"entity_name": "GLI1",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:35:07.860148+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1477",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NUBPL were changed from MITOCHONDRIAL COMPLEX I DEFICIENCY to Mitochondrial complex I deficiency, nuclear type 21 (MIM#618242)",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:34:55.343998+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1476",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NUBPL were set to ",
"entity_name": "NUBPL",
"entity_type": "gene"
},
{
"created": "2021-12-20T16:34:23.806985+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.1475",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NR5A1 as ready",
"entity_name": "NR5A1",
"entity_type": "gene"
}
]
}