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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1136",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=1134",
"results": [
{
"created": "2021-11-09T16:08:58.805702+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BMP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25402547, 22052668, 22482805, 25214535; Phenotypes: Osteogenesis imperfecta, type XIII , MIM#614856; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BMP1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:05:56.393826+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BLM as ready",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:05:56.380326+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: blm has been classified as Green List (High Evidence).",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:05:51.304286+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.322",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BLM were changed from BLOOM SYNDROME to Bloom Syndrome MIM# 210900",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:05:38.999182+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.321",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BLM were set to ",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:05:09.836440+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.320",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BLM: Rating: GREEN; Mode of pathogenicity: None; Publications: 17407155, 9285778, 7585968, 8079989, 12242442, 11101838; Phenotypes: Bloom Syndrome MIM# 210900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BLM",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:03:32.550753+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BIN1 as ready",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:03:32.541487+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bin1 has been classified as Green List (High Evidence).",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:03:23.038474+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9673",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BIN1 were changed from to Centronuclear myopathy 2, MIM# 255200",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:03:04.533777+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9672",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BIN1 were set to ",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:02:45.858785+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9671",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BIN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:02:18.546584+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BIN1: Rating: GREEN; Mode of pathogenicity: None; Publications: 17676042; Phenotypes: Centronuclear myopathy 2, MIM# 255200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:01:45.832883+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.320",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BIN1 were set to 17676042; 17676042",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:58.040886+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.319",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BIN1 as ready",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:58.030066+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.319",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bin1 has been classified as Green List (High Evidence).",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:54.449956+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.319",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BIN1 were changed from CENTRONUCLEAR MYOPATHY 2 to Centronuclear myopathy 2, MIM# 255200",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:42.921339+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.318",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BIN1 were set to ",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:27.565344+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "changed review comment from: ID is generally not part of the phenotype of this myopathy, mild ID reported in one individual only.; to: Variable onset from congenital to childhood. Congenital contractures reported.",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T16:00:02.282622+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BIN1: Changed publications: 17676042, 17676042",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:59:33.969617+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: BIN1: Changed rating: GREEN",
"entity_name": "BIN1",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:57:02.246789+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BHLHA9 as ready",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:57:02.236187+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bhlha9 has been classified as Green List (High Evidence).",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:55:43.283866+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.242",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BHLHA9 were changed from to Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:55:14.379662+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.241",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BHLHA9 were set to ",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:54:48.436233+11:00",
"panel_name": "Polydactyly",
"panel_id": 159,
"panel_version": "0.240",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BHLHA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25466284, 34272776, 31912643, 31152918, 30107244; Phenotypes: Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:54:13.423449+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BHLHA9 as ready",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:54:13.412364+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bhlha9 has been classified as Green List (High Evidence).",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:54:02.175509+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9670",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BHLHA9 were changed from to Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:53:42.342420+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9669",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BHLHA9 were set to ",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:53:19.505520+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9668",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BHLHA9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:52:59.703164+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BHLHA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25466284, 34272776, 31912643, 31152918, 30107244; Phenotypes: Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:52:07.860828+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BHLHA9 as ready",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:52:07.850215+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bhlha9 has been classified as Green List (High Evidence).",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:52:03.902038+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.317",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BHLHA9 were changed from ?Camptosynpolydactyly, complex, OMIM:607539; Syndactyly, mesoaxial synostotic, with phalangeal reduction, OMIM:609432; SPLIT HAND AND FOOT MALFORMATION; MESOAXIAL SYNOSTOTIC SYNDACTYLY WITH PHALANGEAL REDUCTION, MALIK-PERCIN TYPE to Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:51:31.282702+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.316",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BHLHA9 were set to ",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:51:21.218152+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.315",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BHLHA9 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:51:06.527058+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BHLHA9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25466284, 34272776, 31912643, 31152918, 30107244; Phenotypes: Syndactyly, mesoaxial synostotic, with phalangeal reduction, MIM# 609432; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BHLHA9",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:37.873255+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BGN as ready",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:37.863886+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bgn has been classified as Red List (Low Evidence).",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:33.795173+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.314",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BGN were changed from Meester-Loeys syndrome, 300989; X-Linked Spondyloepimetaphyseal Dysplasia; Severe syndromic form of thoracic aortic aneurysm & dissection; Spondyloepimetaphyseal dysplasia, X-linked, 300106 to Spondyloepimetaphyseal dysplasia, X-linked, MIM# 300106",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:19.379048+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.313",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BGN were set to 27236923; 27632686",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:03.698775+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: BGN as Red List (low evidence)",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:47:03.682050+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.312",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bgn has been classified as Red List (Low Evidence).",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:46:49.616155+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.311",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BGN: Rating: RED; Mode of pathogenicity: None; Publications: 27236923; Phenotypes: Spondyloepimetaphyseal dysplasia, X-linked, MIM# 300106; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females",
"entity_name": "BGN",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:56.697955+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLL4 as ready",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:56.687035+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dll4 has been classified as Green List (High Evidence).",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:53.896363+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.56",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLL4 were set to ",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:41.832983+11:00",
"panel_name": "Hand and foot malformations",
"panel_id": 3729,
"panel_version": "0.55",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLL4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26299364, 33899511, 31261205, 29924900; Phenotypes: Adams-Oliver syndrome 6 MIM#616589; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:04.591945+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLL4 as ready",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:04.577221+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dll4 has been classified as Green List (High Evidence).",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:41:01.885367+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.142",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLL4 were changed from to Adams-Oliver syndrome 6 MIM#616589",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:40:32.041867+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.141",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLL4 were set to ",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:39:23.867693+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.140",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DLL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:38:57.678719+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.139",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLL4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26299364, 33899511, 31261205, 29924900; Phenotypes: Adams-Oliver syndrome 6 MIM#616589; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:37:55.578067+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.311",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLL4 were set to 26299364",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:37:34.501492+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLL4 as ready",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:37:34.490360+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dll4 has been classified as Green List (High Evidence).",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:36:32.229786+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9667",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLL4 were changed from to Adams-Oliver syndrome 6, MIM#616589",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:36:08.448276+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9666",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLL4 were set to ",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:34:43.900549+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9665",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DLL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:34:25.778836+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: DLL4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26299364, 33899511, 31261205, 29924900; Phenotypes: Adams-Oliver syndrome 6 MIM#616589; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:31:55.989883+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: DLL4 as ready",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:31:55.980734+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: dll4 has been classified as Green List (High Evidence).",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:31:52.619986+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.310",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: DLL4 were changed from ADAMS-OLIVER SYNDROME 6 to Adams-Oliver syndrome 6, MIM#616589",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:31:37.361980+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.309",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: DLL4 were set to ",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T15:31:26.566884+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.308",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: DLL4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T14:08:51.352630+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.307",
"user_name": "Belinda Chong",
"item_type": "entity",
"text": "reviewed gene: DLL4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26299364; Phenotypes: Adams-Oliver syndrome 6 MIM#616589; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes",
"entity_name": "DLL4",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:51:17.675661+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BFSP2 as ready",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:51:17.662559+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bfsp2 has been classified as Green List (High Evidence).",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:51:14.648348+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.295",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BFSP2 were changed from to Cataract 12, multiple types, MIM# 611597",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:50:51.853817+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.294",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BFSP2 were set to ",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:50:23.221131+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.293",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BFSP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:49:57.854510+11:00",
"panel_name": "Cataract",
"panel_id": 66,
"panel_version": "0.292",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BFSP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10729115, 10739768, 15570218, 24654948, 21836522; Phenotypes: Cataract 12, multiple types, MIM# 611597; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:49:28.648544+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BFSP2 as ready",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:49:28.637521+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bfsp2 has been classified as Green List (High Evidence).",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:49:20.179513+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9664",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BFSP2 were changed from to Cataract 12, multiple types, MIM# 611597",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:49:01.532359+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9663",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BFSP2 were set to ",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:48:44.345042+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9662",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BFSP2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:48:27.866314+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "0.9661",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BFSP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10729115, 10739768, 15570218, 24654948, 21836522; Phenotypes: Cataract 12, multiple types, MIM# 611597; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:47.299357+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BFSP2 as ready",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:47.287349+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bfsp2 has been classified as Green List (High Evidence).",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:43.476839+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.307",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BFSP2 were changed from CATARACT AUTOSOMAL DOMINANT BFSP2-RELATED to Cataract 12, multiple types, MIM# 611597",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:31.867189+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BFSP2 were set to ",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:20.654788+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.305",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BFSP2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:47:09.598150+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BFSP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10729115, 10739768, 15570218, 24654948, 21836522; Phenotypes: Cataract 12, multiple types, MIM# 611597; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BFSP2",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:43:49.719304+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCS1L as ready",
"entity_name": "BCS1L",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:43:49.708836+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcs1l has been classified as Green List (High Evidence).",
"entity_name": "BCS1L",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:43:46.007395+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.304",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCS1L were changed from GRACILE syndrome, 603358; GRACILE SYNDROME to Bjornstad syndrome, MIM# 262000; Leigh syndrome, MIM# 256000; BCS1L-related mitochondrial disease",
"entity_name": "BCS1L",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:43:33.751904+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.303",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BCS1L were set to 30712880",
"entity_name": "BCS1L",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:43:19.120090+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: BCS1L: Rating: GREEN; Mode of pathogenicity: None; Publications: 26563427, 24172246, 17314340; Phenotypes: Bjornstad syndrome, MIM# 262000, Leigh syndrome, MIM# 256000, BCS1L-related mitochondrial disease; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "BCS1L",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:41:20.602244+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCOR as ready",
"entity_name": "BCOR",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:41:20.592920+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcor has been classified as Green List (High Evidence).",
"entity_name": "BCOR",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:41:16.885310+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCOR were changed from MICROPHTHALMIA SYNDROMIC TYPE 2 to Microphthalmia, syndromic 2, MIM# 300166; Oculofaciocardiodental syndrome; Lenz microphthalmia",
"entity_name": "BCOR",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:41:05.478131+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.301",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BCOR were set to ",
"entity_name": "BCOR",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:40:13.482507+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCL11A as ready",
"entity_name": "BCL11A",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:40:13.473319+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: bcl11a has been classified as Green List (High Evidence).",
"entity_name": "BCL11A",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:40:08.873617+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.300",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: BCL11A were changed from INTELLECTUAL DISABILITY to Dias-Logan syndrome, MIM# 617101",
"entity_name": "BCL11A",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:39:57.389064+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.299",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: BCL11A were set to ",
"entity_name": "BCL11A",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:39:46.107042+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.298",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Mode of inheritance for gene: BCL11A was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted",
"entity_name": "BCL11A",
"entity_type": "gene"
},
{
"created": "2021-11-09T13:39:09.979094+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "0.297",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: BCAP31 as ready",
"entity_name": "BCAP31",
"entity_type": "gene"
}
]
}