{"count":221416,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=441","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=439","results":[{"created":"2024-05-30T13:16:48.027771+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGM6 as ready","entity_name":"TGM6","entity_type":"gene"},{"created":"2024-05-30T13:16:48.011482+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm6 has been classified as Red List (Low Evidence).","entity_name":"TGM6","entity_type":"gene"},{"created":"2024-05-30T13:16:42.208492+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TGM6 as Red List (low evidence)","entity_name":"TGM6","entity_type":"gene"},{"created":"2024-05-30T13:16:42.193977+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.230","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgm6 has been classified as Red List (Low Evidence).","entity_name":"TGM6","entity_type":"gene"},{"created":"2024-05-30T13:15:53.108694+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.229","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOR1A as ready","entity_name":"TOR1A","entity_type":"gene"},{"created":"2024-05-30T13:15:53.089027+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1a has been classified as Red List (Low Evidence).","entity_name":"TOR1A","entity_type":"gene"},{"created":"2024-05-30T13:15:48.252680+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.229","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOR1A as Red List (low evidence)","entity_name":"TOR1A","entity_type":"gene"},{"created":"2024-05-30T13:15:48.228278+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.229","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tor1a has been classified as Red List (Low Evidence).","entity_name":"TOR1A","entity_type":"gene"},{"created":"2024-05-30T13:15:00.925453+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSC2 as ready","entity_name":"TSC2","entity_type":"gene"},{"created":"2024-05-30T13:15:00.904871+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc2 has been classified as Red List (Low Evidence).","entity_name":"TSC2","entity_type":"gene"},{"created":"2024-05-30T13:14:56.430422+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TSC2 as Red List (low evidence)","entity_name":"TSC2","entity_type":"gene"},{"created":"2024-05-30T13:14:56.408805+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.228","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tsc2 has been classified as Red List (Low Evidence).","entity_name":"TSC2","entity_type":"gene"},{"created":"2024-05-30T13:14:07.251789+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.227","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TSHR as ready","entity_name":"TSHR","entity_type":"gene"},{"created":"2024-05-30T13:14:07.236539+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.227","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tshr has been classified as Red List (Low Evidence).","entity_name":"TSHR","entity_type":"gene"},{"created":"2024-05-30T13:14:02.196540+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.227","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TSHR as Red List (low evidence)","entity_name":"TSHR","entity_type":"gene"},{"created":"2024-05-30T13:14:02.164558+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.227","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tshr has been classified as Red List (Low Evidence).","entity_name":"TSHR","entity_type":"gene"},{"created":"2024-05-30T12:22:45.816785+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: AAAS: Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"AAAS","entity_type":"gene"},{"created":"2024-05-30T12:22:38.549740+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: AAAS: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"AAAS","entity_type":"gene"},{"created":"2024-05-30T12:22:17.946752+10:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.6","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AAAS: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Achalasia-addisonianism-alacrimia syndrome, MIM# 231550; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"AAAS","entity_type":"gene"},{"created":"2024-05-30T07:20:52.632536+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6019","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SSR4 as ready","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:20:52.618289+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6019","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ssr4 has been classified as Green List (High Evidence).","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:20:48.080869+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6019","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SSR4 were changed from  to Congenital disorder of glycosylation, type Iy, MIM# 300934","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:20:13.115353+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6018","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SSR4 were set to ","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:19:35.460950+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6017","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SSR4 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:18:43.800610+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6016","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SSR4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Iy, MIM# 300934; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"SSR4","entity_type":"gene"},{"created":"2024-05-30T07:17:09.284356+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6016","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RELN as ready","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-30T07:17:09.269748+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6016","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: reln has been classified as Green List (High Evidence).","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-30T07:17:01.601399+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6016","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RELN were set to ","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-30T07:16:12.453521+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6015","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RELN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lissencephaly 2 (Norman-Roberts type), MIM# 257320; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-30T07:15:49.595963+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6015","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RELN were changed from  to Lissencephaly 2 (Norman-Roberts type), MIM# 257320","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-30T07:15:11.257010+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6014","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RELN was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-29T22:29:02.765373+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6013","user_name":"Anissa Johnson","item_type":"entity","text":"Deleted their review","entity_name":"SLC35A1","entity_type":"gene"},{"created":"2024-05-29T20:37:25.514896+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6013","user_name":"Tashunka Taylor-Miller","item_type":"entity","text":"changed review comment from: 7 individuals from 4 families with biallelic variants, and 13 individuals from 7 families with monoallelic (heterozygous) variants of RELN and frontotemporal or temporal-predominant lissencephaly variant. Associated features: intellectual disability (16/20), seizures (5/20), unprovoked aggression (6/20), sleep disturbance (7/20)\r\nVariant spectrum includes: loss of function, missense, splice-site variants.\r\n\r\nMRI features include: anterior-predominant “thin”lisencephaly pachygyria with cerebellar hypoplasia\r\nBiallelic variants are associated with a severe phenotype that includes cerebellar hypoplasia. \r\nMonoallelic variants are associated with incomplete penetrance and variable expressivity (eg: one adult with abnormal MRI but normal intelligence and neurological profile).; to: 7 individuals from 4 families with biallelic variants, and 13 individuals from 7 families with monoallelic (heterozygous) variants of RELN and frontotemporal or temporal-predominant lissencephaly variant. Associated features: intellectual disability (16/20), seizures (5/20), unprovoked aggression (6/20), sleep disturbance (7/20)\r\nVariant spectrum includes: loss of function, missense, splice-site variants.\r\n\r\nMRI features include: anterior-predominant “thin” lisencephaly pachygyria with cerebellar hypoplasia.\r\nBiallelic variants are associated with a severe phenotype that includes cerebellar hypoplasia. \r\nMonoallelic variants are associated with incomplete penetrance and variable expressivity (eg: one adult with abnormal MRI but normal intelligence and neurological profile).","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-29T20:36:36.202469+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6013","user_name":"Tashunka Taylor-Miller","item_type":"entity","text":"edited their review of gene: RELN: Changed publications: PMID: 35769015, PMID: 29671837","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-29T20:36:10.364283+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.6013","user_name":"Tashunka Taylor-Miller","item_type":"entity","text":"reviewed gene: RELN: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 35769015, 29671837; Phenotypes: OMIM *600514, HP:0001339, DOID:0070338; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"RELN","entity_type":"gene"},{"created":"2024-05-29T18:03:43.248375+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CTCF as ready","entity_name":"CTCF","entity_type":"gene"},{"created":"2024-05-29T18:03:43.229537+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctcf has been classified as Red List (Low Evidence).","entity_name":"CTCF","entity_type":"gene"},{"created":"2024-05-29T18:03:37.579812+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CTCF as Red List (low evidence)","entity_name":"CTCF","entity_type":"gene"},{"created":"2024-05-29T18:03:37.566999+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.226","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ctcf has been classified as Red List (Low Evidence).","entity_name":"CTCF","entity_type":"gene"},{"created":"2024-05-29T18:02:40.183528+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.225","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLCN7 as ready","entity_name":"CLCN7","entity_type":"gene"},{"created":"2024-05-29T18:02:40.167483+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.225","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn7 has been classified as Red List (Low Evidence).","entity_name":"CLCN7","entity_type":"gene"},{"created":"2024-05-29T18:02:31.832428+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.225","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLCN7 as Red List (low evidence)","entity_name":"CLCN7","entity_type":"gene"},{"created":"2024-05-29T18:02:31.801006+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.225","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clcn7 has been classified as Red List (Low Evidence).","entity_name":"CLCN7","entity_type":"gene"},{"created":"2024-05-29T18:01:43.268678+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHD7 as ready","entity_name":"CHD7","entity_type":"gene"},{"created":"2024-05-29T18:01:43.253307+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd7 has been classified as Amber List (Moderate Evidence).","entity_name":"CHD7","entity_type":"gene"},{"created":"2024-05-29T18:01:34.322962+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHD7 as Amber List (moderate evidence)","entity_name":"CHD7","entity_type":"gene"},{"created":"2024-05-29T18:01:34.309473+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.224","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd7 has been classified as Amber List (Moderate Evidence).","entity_name":"CHD7","entity_type":"gene"},{"created":"2024-05-29T18:00:48.353920+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.223","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHD4 as ready","entity_name":"CHD4","entity_type":"gene"},{"created":"2024-05-29T18:00:48.337424+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.223","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd4 has been classified as Red List (Low Evidence).","entity_name":"CHD4","entity_type":"gene"},{"created":"2024-05-29T18:00:43.882507+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.223","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHD4 as Red List (low evidence)","entity_name":"CHD4","entity_type":"gene"},{"created":"2024-05-29T18:00:43.869109+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.223","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chd4 has been classified as Red List (Low Evidence).","entity_name":"CHD4","entity_type":"gene"},{"created":"2024-05-29T17:59:57.426692+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHCHD10 as ready","entity_name":"CHCHD10","entity_type":"gene"},{"created":"2024-05-29T17:59:57.403247+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chchd10 has been classified as Red List (Low Evidence).","entity_name":"CHCHD10","entity_type":"gene"},{"created":"2024-05-29T17:59:52.148554+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHCHD10 as Red List (low evidence)","entity_name":"CHCHD10","entity_type":"gene"},{"created":"2024-05-29T17:59:52.134578+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.222","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chchd10 has been classified as Red List (Low Evidence).","entity_name":"CHCHD10","entity_type":"gene"},{"created":"2024-05-29T17:59:06.102977+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.221","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CAMK2G as ready","entity_name":"CAMK2G","entity_type":"gene"},{"created":"2024-05-29T17:59:06.090933+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.221","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: camk2g has been classified as Red List (Low Evidence).","entity_name":"CAMK2G","entity_type":"gene"},{"created":"2024-05-29T17:59:01.601145+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.221","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CAMK2G as Red List (low evidence)","entity_name":"CAMK2G","entity_type":"gene"},{"created":"2024-05-29T17:59:01.586302+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.221","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: camk2g has been classified as Red List (Low Evidence).","entity_name":"CAMK2G","entity_type":"gene"},{"created":"2024-05-29T17:58:16.552323+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CAMK2B as ready","entity_name":"CAMK2B","entity_type":"gene"},{"created":"2024-05-29T17:58:16.538786+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: camk2b has been classified as Red List (Low Evidence).","entity_name":"CAMK2B","entity_type":"gene"},{"created":"2024-05-29T17:58:11.532395+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CAMK2B as Red List (low evidence)","entity_name":"CAMK2B","entity_type":"gene"},{"created":"2024-05-29T17:58:11.507375+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.220","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: camk2b has been classified as Red List (Low Evidence).","entity_name":"CAMK2B","entity_type":"gene"},{"created":"2024-05-29T17:57:28.678095+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.219","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CACNA1G as ready","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2024-05-29T17:57:28.665492+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.219","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1g has been classified as Green List (High Evidence).","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2024-05-29T17:57:14.650254+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.219","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CACNA1G as Green List (high evidence)","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2024-05-29T17:57:14.613295+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.219","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1g has been classified as Green List (High Evidence).","entity_name":"CACNA1G","entity_type":"gene"},{"created":"2024-05-29T17:56:31.479151+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CACNA1D as ready","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2024-05-29T17:56:31.464465+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1d has been classified as Amber List (Moderate Evidence).","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2024-05-29T17:56:26.077735+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CACNA1D as Amber List (moderate evidence)","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2024-05-29T17:56:26.063628+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.218","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cacna1d has been classified as Amber List (Moderate Evidence).","entity_name":"CACNA1D","entity_type":"gene"},{"created":"2024-05-29T17:55:35.707384+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.217","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP6V1A as ready","entity_name":"ATP6V1A","entity_type":"gene"},{"created":"2024-05-29T17:55:35.694968+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.217","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp6v1a has been classified as Red List (Low Evidence).","entity_name":"ATP6V1A","entity_type":"gene"},{"created":"2024-05-29T17:55:31.188695+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.217","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATP6V1A as Red List (low evidence)","entity_name":"ATP6V1A","entity_type":"gene"},{"created":"2024-05-29T17:55:31.171194+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.217","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp6v1a has been classified as Red List (Low Evidence).","entity_name":"ATP6V1A","entity_type":"gene"},{"created":"2024-05-29T17:54:40.603872+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ATP1A2 as ready","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2024-05-29T17:54:40.592110+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp1a2 has been classified as Red List (Low Evidence).","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2024-05-29T17:54:36.035025+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ATP1A2 as Red List (low evidence)","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2024-05-29T17:54:36.019260+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.216","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: atp1a2 has been classified as Red List (Low Evidence).","entity_name":"ATP1A2","entity_type":"gene"},{"created":"2024-05-29T17:53:55.465278+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.215","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARID1B as ready","entity_name":"ARID1B","entity_type":"gene"},{"created":"2024-05-29T17:53:55.452453+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.215","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arid1b has been classified as Red List (Low Evidence).","entity_name":"ARID1B","entity_type":"gene"},{"created":"2024-05-29T17:53:48.380261+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.215","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARID1B as Red List (low evidence)","entity_name":"ARID1B","entity_type":"gene"},{"created":"2024-05-29T17:53:48.369081+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.215","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: arid1b has been classified as Red List (Low Evidence).","entity_name":"ARID1B","entity_type":"gene"},{"created":"2024-05-29T16:58:25.607642+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DNM2 as ready","entity_name":"DNM2","entity_type":"gene"},{"created":"2024-05-29T16:58:25.593548+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnm2 has been classified as Red List (Low Evidence).","entity_name":"DNM2","entity_type":"gene"},{"created":"2024-05-29T16:58:17.938399+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DNM2 as Red List (low evidence)","entity_name":"DNM2","entity_type":"gene"},{"created":"2024-05-29T16:58:17.922475+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.214","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dnm2 has been classified as Red List (Low Evidence).","entity_name":"DNM2","entity_type":"gene"},{"created":"2024-05-29T16:44:16.911848+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.213","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TUBB4A were set to 34531397; 33528536","entity_name":"TUBB4A","entity_type":"gene"},{"created":"2024-05-29T16:43:29.901310+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TUBG1 as ready","entity_name":"TUBG1","entity_type":"gene"},{"created":"2024-05-29T16:43:29.888185+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubg1 has been classified as Red List (Low Evidence).","entity_name":"TUBG1","entity_type":"gene"},{"created":"2024-05-29T16:43:24.668407+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TUBG1 as Red List (low evidence)","entity_name":"TUBG1","entity_type":"gene"},{"created":"2024-05-29T16:43:24.652607+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.212","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tubg1 has been classified as Red List (Low Evidence).","entity_name":"TUBG1","entity_type":"gene"},{"created":"2024-05-29T16:42:40.763058+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.211","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE3A were set to PMID: 33528536","entity_name":"UBE3A","entity_type":"gene"},{"created":"2024-05-29T16:41:53.327916+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZBTB18 as ready","entity_name":"ZBTB18","entity_type":"gene"},{"created":"2024-05-29T16:41:53.310767+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb18 has been classified as Red List (Low Evidence).","entity_name":"ZBTB18","entity_type":"gene"},{"created":"2024-05-29T16:41:47.257217+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZBTB18 as Red List (low evidence)","entity_name":"ZBTB18","entity_type":"gene"},{"created":"2024-05-29T16:41:47.233413+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.210","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zbtb18 has been classified as Red List (Low Evidence).","entity_name":"ZBTB18","entity_type":"gene"},{"created":"2024-05-29T16:40:58.124655+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.209","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZEB2 were set to 33528536; 33098801","entity_name":"ZEB2","entity_type":"gene"},{"created":"2024-05-29T16:40:07.291849+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.208","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ITPR1 were set to 28826917; 25981959; 22986007","entity_name":"ITPR1","entity_type":"gene"},{"created":"2024-05-29T16:39:14.042124+10:00","panel_name":"Cerebral Palsy","panel_id":73,"panel_version":"1.207","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SPTBN2 were set to 31066025; 25981959; 31721007","entity_name":"SPTBN2","entity_type":"gene"}]}