{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1136","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&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"}]}