{"count":221278,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1048","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1046","results":[{"created":"2022-01-14T16:24:40.805653+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2200","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: DCC: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 20431009, 31697046, 21242494, 28250454, 28250456; Phenotypes: Mirror movements 1 and/or agenesis of the corpus callosum, OMIM #157600, Gaze palsy, familial horizontal, with progressive scoliosis, 2,OMIM # 617542; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DCC","entity_type":"gene"},{"created":"2022-01-14T16:09:35.539559+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2200","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TAC3 as Red List (low evidence)","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-01-14T16:09:35.526529+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2200","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tac3 has been classified as Red List (Low Evidence).","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-01-14T16:09:16.431430+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2199","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TAC3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TAC3","entity_type":"gene"},{"created":"2022-01-14T16:07:18.409178+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2199","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TNFRSF13B as Red List (low evidence)","entity_name":"TNFRSF13B","entity_type":"gene"},{"created":"2022-01-14T16:07:18.398691+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2199","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tnfrsf13b has been classified as Red List (Low Evidence).","entity_name":"TNFRSF13B","entity_type":"gene"},{"created":"2022-01-14T16:07:17.382110+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2199","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TNFRSF13B as Red List (low evidence)","entity_name":"TNFRSF13B","entity_type":"gene"},{"created":"2022-01-14T16:07:17.369060+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2199","user_name":"Chirag Patel","item_type":"entity","text":"Gene: tnfrsf13b has been classified as Red List (Low Evidence).","entity_name":"TNFRSF13B","entity_type":"gene"},{"created":"2022-01-14T16:06:55.957605+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2198","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TNFRSF13B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TNFRSF13B","entity_type":"gene"},{"created":"2022-01-14T15:56:12.212892+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2198","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: NXN as Green List (high evidence)","entity_name":"NXN","entity_type":"gene"},{"created":"2022-01-14T15:56:12.201140+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2198","user_name":"Chirag Patel","item_type":"entity","text":"Gene: nxn has been classified as Green List (High Evidence).","entity_name":"NXN","entity_type":"gene"},{"created":"2022-01-14T15:55:57.272735+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2197","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: NXN: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 29276006, 32954672, 33048444; Phenotypes: Robinow syndrome, autosomal recessive 2, OMIM #618529; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NXN","entity_type":"gene"},{"created":"2022-01-14T15:36:23.002372+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2197","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SNX10 as Red List (low evidence)","entity_name":"SNX10","entity_type":"gene"},{"created":"2022-01-14T15:36:22.985447+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2197","user_name":"Chirag Patel","item_type":"entity","text":"Gene: snx10 has been classified as Red List (Low Evidence).","entity_name":"SNX10","entity_type":"gene"},{"created":"2022-01-14T15:36:13.358440+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2196","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SNX10: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SNX10","entity_type":"gene"},{"created":"2022-01-14T15:32:36.395053+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2196","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SOX11 as Green List (high evidence)","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:32:36.383681+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2196","user_name":"Chirag Patel","item_type":"entity","text":"Gene: sox11 has been classified as Green List (High Evidence).","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:32:27.663569+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4435","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SOX11: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 24886874, 33785884, 33430815, 33086258, 31530938; Phenotypes: Coffin-Siris syndrome 9, OMIM # 615866; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:32:04.204803+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2195","user_name":"Chirag Patel","item_type":"entity","text":"Deleted their comment","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:31:56.082184+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2195","user_name":"Chirag Patel","item_type":"entity","text":"edited their review of gene: SOX11: Added comment: Coffin-Siris syndrome is characterized by mild intellectual disability, dysmorphic facial features, hypertrichosis, microcephaly, growth deficiency, and hypoplastic fifth toenails. sox11a/b knockdown in zebrafish causes brain abnormalities, potentially explaining the brain phenotype of CSS. Numerous cases reported with heterozygous mutations. Can present with IUGR antenatally. Suitable for fetal anomalies panel.; Changed publications: PubMed: 24886874, 33785884, 33430815, 33086258,  31530938","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:26:30.945542+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2195","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SOX11: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 24886874, 33785884; Phenotypes: Coffin-Siris syndrome 9, OMIM # 615866; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SOX11","entity_type":"gene"},{"created":"2022-01-14T15:15:29.319285+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2195","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: MEOX1 as Green List (high evidence)","entity_name":"MEOX1","entity_type":"gene"},{"created":"2022-01-14T15:15:29.302906+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2195","user_name":"Chirag Patel","item_type":"entity","text":"Gene: meox1 has been classified as Green List (High Evidence).","entity_name":"MEOX1","entity_type":"gene"},{"created":"2022-01-14T15:15:19.926296+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.152","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: MEOX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 24073994, 23290072; Phenotypes: Klippel-Feil syndrome 2, OMIM #214300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEOX1","entity_type":"gene"},{"created":"2022-01-14T15:14:45.959672+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2194","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: MEOX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 24073994, 23290072; Phenotypes: Klippel-Feil syndrome 2, OMIM #214300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"MEOX1","entity_type":"gene"},{"created":"2022-01-14T15:08:11.007307+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2194","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: OTUD6B as Green List (high evidence)","entity_name":"OTUD6B","entity_type":"gene"},{"created":"2022-01-14T15:08:10.995273+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2194","user_name":"Chirag Patel","item_type":"entity","text":"Gene: otud6b has been classified as Green List (High Evidence).","entity_name":"OTUD6B","entity_type":"gene"},{"created":"2022-01-14T15:08:00.287190+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2193","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: OTUD6B: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 28343629, 32924626, 31147255; Phenotypes: Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies, OMIM #617452; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTUD6B","entity_type":"gene"},{"created":"2022-01-14T15:07:58.419310+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4435","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: OTUD6B: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 28343629, 32924626, 31147255; Phenotypes: Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies, OMIM #617452; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTUD6B","entity_type":"gene"},{"created":"2022-01-14T14:59:10.129070+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2193","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SGCG as Red List (low evidence)","entity_name":"SGCG","entity_type":"gene"},{"created":"2022-01-14T14:59:10.113252+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2193","user_name":"Chirag Patel","item_type":"entity","text":"Gene: sgcg has been classified as Red List (Low Evidence).","entity_name":"SGCG","entity_type":"gene"},{"created":"2022-01-14T14:58:58.015152+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2192","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SGCG: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SGCG","entity_type":"gene"},{"created":"2022-01-14T14:57:50.302317+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2192","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SLC6A17 as Red List (low evidence)","entity_name":"SLC6A17","entity_type":"gene"},{"created":"2022-01-14T14:57:50.289616+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2192","user_name":"Chirag Patel","item_type":"entity","text":"Gene: slc6a17 has been classified as Red List (Low Evidence).","entity_name":"SLC6A17","entity_type":"gene"},{"created":"2022-01-14T14:57:40.619551+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2191","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SLC6A17: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SLC6A17","entity_type":"gene"},{"created":"2022-01-14T14:57:03.424175+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2191","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: RAB33B as Red List (low evidence)","entity_name":"RAB33B","entity_type":"gene"},{"created":"2022-01-14T14:57:03.411841+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2191","user_name":"Chirag Patel","item_type":"entity","text":"Gene: rab33b has been classified as Red List (Low Evidence).","entity_name":"RAB33B","entity_type":"gene"},{"created":"2022-01-14T14:56:11.345145+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2190","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: RAB33B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"RAB33B","entity_type":"gene"},{"created":"2022-01-14T14:54:25.886189+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2190","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SERPINH1 as Red List (low evidence)","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2022-01-14T14:54:25.877364+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2190","user_name":"Chirag Patel","item_type":"entity","text":"Gene: serpinh1 has been classified as Red List (Low Evidence).","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2022-01-14T14:54:13.373748+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2189","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SERPINH1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SERPINH1","entity_type":"gene"},{"created":"2022-01-14T14:52:36.630009+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2189","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SERPINF1 as Red List (low evidence)","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:36.619873+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2189","user_name":"Chirag Patel","item_type":"entity","text":"Gene: serpinf1 has been classified as Red List (Low Evidence).","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:34.313949+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2188","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SERPINF1 as Red List (low evidence)","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:34.304761+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2188","user_name":"Chirag Patel","item_type":"entity","text":"Gene: serpinf1 has been classified as Red List (Low Evidence).","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:33.895115+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2188","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SERPINF1 as Red List (low evidence)","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:33.882934+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2188","user_name":"Chirag Patel","item_type":"entity","text":"Gene: serpinf1 has been classified as Red List (Low Evidence).","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:52:18.609992+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2187","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SERPINF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SERPINF1","entity_type":"gene"},{"created":"2022-01-14T14:40:15.659272+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2187","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TMEM38B: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 23316006, 23054245,  26911354,  34902613; Phenotypes: Osteogenesis imperfecta, type XIV , OMIM #615066; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMEM38B","entity_type":"gene"},{"created":"2022-01-14T14:28:37.496088+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2187","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: POLR3A as Red List (low evidence)","entity_name":"POLR3A","entity_type":"gene"},{"created":"2022-01-14T14:28:37.484642+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2187","user_name":"Chirag Patel","item_type":"entity","text":"Gene: polr3a has been classified as Red List (Low Evidence).","entity_name":"POLR3A","entity_type":"gene"},{"created":"2022-01-14T14:28:26.740399+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2186","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: POLR3A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"POLR3A","entity_type":"gene"},{"created":"2022-01-14T14:26:38.849022+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2186","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: POLR3B as Red List (low evidence)","entity_name":"POLR3B","entity_type":"gene"},{"created":"2022-01-14T14:26:38.837431+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2186","user_name":"Chirag Patel","item_type":"entity","text":"Gene: polr3b has been classified as Red List (Low Evidence).","entity_name":"POLR3B","entity_type":"gene"},{"created":"2022-01-14T14:26:26.281165+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2185","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: POLR3B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"POLR3B","entity_type":"gene"},{"created":"2022-01-14T14:26:04.917245+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2185","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PYCR2 as Red List (low evidence)","entity_name":"PYCR2","entity_type":"gene"},{"created":"2022-01-14T14:26:04.903000+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2185","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pycr2 has been classified as Red List (Low Evidence).","entity_name":"PYCR2","entity_type":"gene"},{"created":"2022-01-14T14:25:53.799957+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2184","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PYCR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PYCR2","entity_type":"gene"},{"created":"2022-01-14T14:13:02.915361+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2184","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PITX1 as Green List (high evidence)","entity_name":"PITX1","entity_type":"gene"},{"created":"2022-01-14T14:13:02.899214+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2184","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pitx1 has been classified as Green List (High Evidence).","entity_name":"PITX1","entity_type":"gene"},{"created":"2022-01-14T14:12:51.943464+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2183","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PITX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 21775501, 22258522, 18950742; Phenotypes: Clubfoot, congenital, with or without deficiency of long bones and/or mirror-image polydactyly, OMIM #119800, Liebenberg syndrome , OMIM #186550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PITX1","entity_type":"gene"},{"created":"2022-01-14T14:08:49.650555+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10627","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: ICAM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes","entity_name":"ICAM1","entity_type":"gene"},{"created":"2022-01-14T14:06:15.049329+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10627","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: IRAK3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes","entity_name":"IRAK3","entity_type":"gene"},{"created":"2022-01-14T14:04:14.241507+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2183","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: FEZF1 as Red List (low evidence)","entity_name":"FEZF1","entity_type":"gene"},{"created":"2022-01-14T14:04:14.219721+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2183","user_name":"Chirag Patel","item_type":"entity","text":"Gene: fezf1 has been classified as Red List (Low Evidence).","entity_name":"FEZF1","entity_type":"gene"},{"created":"2022-01-14T14:04:01.927190+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2182","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: FEZF1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"FEZF1","entity_type":"gene"},{"created":"2022-01-14T13:51:09.286327+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2182","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: NAXE as Red List (low evidence)","entity_name":"NAXE","entity_type":"gene"},{"created":"2022-01-14T13:51:09.274708+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2182","user_name":"Chirag Patel","item_type":"entity","text":"Gene: naxe has been classified as Red List (Low Evidence).","entity_name":"NAXE","entity_type":"gene"},{"created":"2022-01-14T13:51:07.913743+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2182","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: NAXE as Red List (low evidence)","entity_name":"NAXE","entity_type":"gene"},{"created":"2022-01-14T13:51:07.901882+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2182","user_name":"Chirag Patel","item_type":"entity","text":"Gene: naxe has been classified as Red List (Low Evidence).","entity_name":"NAXE","entity_type":"gene"},{"created":"2022-01-14T13:50:53.653223+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2181","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: NAXE: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"NAXE","entity_type":"gene"},{"created":"2022-01-14T13:49:47.023304+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2181","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TRMT10C as Red List (low evidence)","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2022-01-14T13:49:47.011829+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2181","user_name":"Chirag Patel","item_type":"entity","text":"Gene: trmt10c has been classified as Red List (Low Evidence).","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2022-01-14T13:49:37.627910+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2180","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TRMT10C: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TRMT10C","entity_type":"gene"},{"created":"2022-01-14T13:47:52.702333+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2180","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PBX1 as Green List (high evidence)","entity_name":"PBX1","entity_type":"gene"},{"created":"2022-01-14T13:47:52.687808+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2180","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pbx1 has been classified as Green List (High Evidence).","entity_name":"PBX1","entity_type":"gene"},{"created":"2022-01-14T13:47:39.307643+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2179","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PBX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 28566479, 29036646; Phenotypes: Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay, OMIM #617641; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PBX1","entity_type":"gene"},{"created":"2022-01-14T13:47:37.850075+11:00","panel_name":"Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic","panel_id":63,"panel_version":"0.102","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PBX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 28566479, 29036646; Phenotypes: Congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay, OMIM #617641; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PBX1","entity_type":"gene"},{"created":"2022-01-14T13:42:28.148109+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2179","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PFKM as Red List (low evidence)","entity_name":"PFKM","entity_type":"gene"},{"created":"2022-01-14T13:42:28.137150+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2179","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pfkm has been classified as Red List (Low Evidence).","entity_name":"PFKM","entity_type":"gene"},{"created":"2022-01-14T13:42:16.861921+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2178","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PFKM: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PFKM","entity_type":"gene"},{"created":"2022-01-14T13:41:20.863553+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2178","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: TRPM7 as Red List (low evidence)","entity_name":"TRPM7","entity_type":"gene"},{"created":"2022-01-14T13:41:20.852325+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2178","user_name":"Chirag Patel","item_type":"entity","text":"Gene: trpm7 has been classified as Red List (Low Evidence).","entity_name":"TRPM7","entity_type":"gene"},{"created":"2022-01-14T13:41:09.804558+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2177","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: TRPM7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"TRPM7","entity_type":"gene"},{"created":"2022-01-14T13:40:07.931506+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2177","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: PTH as Red List (low evidence)","entity_name":"PTH","entity_type":"gene"},{"created":"2022-01-14T13:40:07.919964+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2177","user_name":"Chirag Patel","item_type":"entity","text":"Gene: pth has been classified as Red List (Low Evidence).","entity_name":"PTH","entity_type":"gene"},{"created":"2022-01-14T13:39:54.631748+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2176","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: PTH: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"PTH","entity_type":"gene"},{"created":"2022-01-14T13:38:53.432117+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2176","user_name":"Chirag Patel","item_type":"entity","text":"Classified gene: SET as Red List (low evidence)","entity_name":"SET","entity_type":"gene"},{"created":"2022-01-14T13:38:53.410134+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2176","user_name":"Chirag Patel","item_type":"entity","text":"Gene: set has been classified as Red List (Low Evidence).","entity_name":"SET","entity_type":"gene"},{"created":"2022-01-14T13:38:42.650137+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2175","user_name":"Chirag Patel","item_type":"entity","text":"reviewed gene: SET: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SET","entity_type":"gene"},{"created":"2022-01-14T12:35:11.715182+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.10627","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CAPN10: Rating: RED; Mode of pathogenicity: None; Publications: 31791003, 31292430; Phenotypes: ; Mode of inheritance: None; Current diagnostic: yes","entity_name":"CAPN10","entity_type":"gene"},{"created":"2022-01-14T10:18:16.792768+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2175","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:ZNF750 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:17:24.221173+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2174","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:UVSSA from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:16:47.089473+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2173","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:USB1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:16:17.022034+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2172","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:UROS from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:15:56.714341+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2171","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:UGT1A1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:15:20.669449+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2170","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TYRP1 from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:15:06.371413+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2169","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TYR from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:14:42.692019+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2168","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TSHR from the panel","entity_name":null,"entity_type":null},{"created":"2022-01-14T10:14:25.867173+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"0.2167","user_name":"Zornitza Stark","item_type":"panel","text":"removed gene:TSHB from the panel","entity_name":null,"entity_type":null}]}