{"count":221415,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1809","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1807","results":[{"created":"2020-05-04T20:54:52.410560+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC28B were set to ","entity_name":"CCDC28B","entity_type":"gene"},{"created":"2020-05-04T20:54:19.252465+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC28B as Amber List (moderate evidence)","entity_name":"CCDC28B","entity_type":"gene"},{"created":"2020-05-04T20:54:19.243929+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc28b has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC28B","entity_type":"gene"},{"created":"2020-05-04T20:53:10.088691+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C21orf59 as ready","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:53:10.084577+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: p.Tyr245* recurrent in the Ashkenazi Jewish population","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:53:10.064371+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c21orf59 has been classified as Green List (High Evidence).","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:52:33.226444+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:52:05.053441+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C21orf59 as ready","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:52:05.048375+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: p.Tyr245* recurring in the Ashkenazi Jewish population","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:52:05.022656+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c21orf59 has been classified as Green List (High Evidence).","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:51:33.858163+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:50:50.478716+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: C21orf59.","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:50:41.871203+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C21orf59 were set to 24094744","entity_name":"C21orf59","entity_type":"gene"},{"created":"2020-05-04T20:49:08.534866+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VPS13B as ready","entity_name":"VPS13B","entity_type":"gene"},{"created":"2020-05-04T20:49:08.529288+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Agree retinopathy, obesity and ID overlap significantly with typical phenotypic features of ciliopathies, therefore reasonable to include in this panel even though not strictly a ciliopathy.","entity_name":"VPS13B","entity_type":"gene"},{"created":"2020-05-04T20:49:08.486586+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps13b has been classified as Amber List (Moderate Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2020-05-04T20:47:58.627516+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: VPS13B as Amber List (moderate evidence)","entity_name":"VPS13B","entity_type":"gene"},{"created":"2020-05-04T20:47:58.615613+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vps13b has been classified as Amber List (Moderate Evidence).","entity_name":"VPS13B","entity_type":"gene"},{"created":"2020-05-04T20:45:40.827176+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C11orf70 as ready","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:45:40.818375+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c11orf70 has been classified as Green List (High Evidence).","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:45:29.957104+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C11orf70.","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:45:14.800246+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2729","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C11orf70 were changed from  to Ciliary dyskinesia, primary, 38, MIM# 618063","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:44:50.796924+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2728","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C11orf70 were set to ","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:44:31.305234+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2727","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C11orf70 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:44:09.652209+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2726","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C11orf70: Rating: GREEN; Mode of pathogenicity: None; Publications: 29727693, 29727692; Phenotypes: Ciliary dyskinesia, primary, 38, MIM# 618063; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:43:18.762777+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C11orf70.","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:43:11.635854+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C11orf70 as ready","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:43:11.624388+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c11orf70 has been classified as Green List (High Evidence).","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:43:09.247136+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C11orf70 were changed from  to Ciliary dyskinesia, primary, 38, MIM# 618063","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:42:40.339753+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C11orf70 were set to ","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:42:10.690240+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C11orf70 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:41:40.324726+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: C11orf70: Rating: GREEN; Mode of pathogenicity: None; Publications: 29727693, 29727692; Phenotypes: Ciliary dyskinesia, primary, 38, MIM# 618063; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:40:49.725273+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Tag new gene name tag was added to gene: C11orf70.","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:39:42.709288+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C11orf70 as ready","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:39:42.699138+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c11orf70 has been classified as Green List (High Evidence).","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:38:59.003175+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: C11orf70 as Green List (high evidence)","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:38:58.990171+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c11orf70 has been classified as Green List (High Evidence).","entity_name":"C11orf70","entity_type":"gene"},{"created":"2020-05-04T20:38:25.516615+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2618","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARMC9 were changed from  to Joubert syndrome 30, MIM# 617622","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:37:52.035919+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2617","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARMC9 were set to ","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:37:19.818699+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2616","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARMC9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:36:44.880585+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2615","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC9: Rating: GREEN; Mode of pathogenicity: None; Publications: 28625504; Phenotypes: Joubert syndrome 30, MIM# 617622; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:36:36.489771+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC9 as ready","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:36:36.480955+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc9 has been classified as Green List (High Evidence).","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:36:18.260056+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC9 as Green List (high evidence)","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:36:18.248981+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc9 has been classified as Green List (High Evidence).","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:35:21.501888+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2726","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC9 as ready","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:35:21.493074+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2726","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc9 has been classified as Green List (High Evidence).","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:35:10.780252+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2726","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARMC9 were changed from  to Joubert syndrome 30, MIM#617622","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:34:49.075750+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2725","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARMC9 were set to ","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:34:29.416160+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2724","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARMC9 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:34:06.778843+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their comment","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:33:54.699363+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ARMC9: Added comment: ARMC9 localizes to the ciliary basal body and daughter centriole and is predicted to function in ciliogenesis PMID: 28625504 - 8 families with Joubert syndrome, all variant types detected. Functional studies show protein localizes at the basal body and upregulates during ciliogenesis. Zebrafish with frameshift mutation recapitulated the human phenotype including a curved body, coloboma, retinal dystrophy and less cilia.; Changed rating: GREEN; Changed publications: 28625504","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:33:12.374368+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"gene: ARMC9 was added\ngene: ARMC9 was added to Joubert syndrome and other neurological ciliopathies. Sources: Expert list\nMode of inheritance for gene: ARMC9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: ARMC9 were set to 28625504\nPhenotypes for gene: ARMC9 were set to Joubert syndrome 30, MIM#\t617622\nReview for gene: ARMC9 was set to GREEN\nAdded comment: ARMC9 localizes to the ciliary basal body and daughter centriole and is predicted to function in ciliogenesis PMID: 28625504 - 8 families with Joubert syndrome, all variant types detected. Functional studies show protein localizes at the basal body and upregulates during ciliogenesis. Zebrafish with frameshift mutation recapitulated the human phenotype including a curved body, coloboma, retinal dystrophy and less cilia. \nSources: Expert list","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:32:29.983362+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC9 as ready","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:32:29.974842+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc9 has been classified as Green List (High Evidence).","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:31:40.693256+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC9 as Green List (high evidence)","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:31:40.679348+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc9 has been classified as Green List (High Evidence).","entity_name":"ARMC9","entity_type":"gene"},{"created":"2020-05-04T20:30:39.768833+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC8 as ready","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:30:39.760217+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:30:36.145827+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC8 as Red List (low evidence)","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:30:36.137246+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:30:06.562320+10:00","panel_name":"Polydactyly","panel_id":159,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:29:40.542760+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC8 as ready","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:29:40.528901+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:29:32.271476+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC8 as Red List (low evidence)","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:29:32.263028+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2723","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:29:12.458032+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2722","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:28:46.667407+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC8 as ready","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:28:46.653143+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:28:42.602298+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC8 as Red List (low evidence)","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:28:42.588582+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:28:13.119228+10:00","panel_name":"Joubert syndrome and other neurological ciliopathies","panel_id":129,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:27:32.808798+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2722","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC4 as ready","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:27:32.799838+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2722","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc4 has been classified as Green List (High Evidence).","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:27:29.416255+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC8 as ready","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:27:29.402936+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:26:52.459899+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ARMC8 as Red List (low evidence)","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:26:52.448513+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc8 has been classified as Red List (Low Evidence).","entity_name":"ARMC8","entity_type":"gene"},{"created":"2020-05-04T20:26:02.776446+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2722","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARMC4 were changed from  to Ciliary dyskinesia, primary, 23, MIM# 615451","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:47.792763+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ARMC4 as ready","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:47.784189+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: armc4 has been classified as Green List (High Evidence).","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:41.454587+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2721","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARMC4 were set to ","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:25.349484+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2720","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARMC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:05.280007+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2719","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 31765523, 23849778; Phenotypes: Ciliary dyskinesia, primary, 23, MIM# 615451; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:25:03.946112+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARMC4 were changed from  to Ciliary dyskinesia, primary, 23, MIM# 615451","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:24:18.467755+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARMC4 were set to ","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:23:54.999793+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARMC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:23:23.057811+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: ARMC4: Changed publications: 31765523, 23849778","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:23:12.341659+10:00","panel_name":"Heterotaxy","panel_id":108,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ARMC4: Rating: GREEN; Mode of pathogenicity: None; Publications: 31765523; Phenotypes: Ciliary dyskinesia, primary, 23, MIM# 615451; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:22:24.632346+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ARMC4 were changed from  to Ciliary dyskinesia, primary, 23, MIM# 615451","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:21:52.638691+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ARMC4 were set to ","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:21:29.726011+10:00","panel_name":"Ciliary Dyskinesia","panel_id":82,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ARMC4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ARMC4","entity_type":"gene"},{"created":"2020-05-04T20:20:26.809083+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZSWIM6 were changed from Acromelic frontonasal dysostosis (MIM#603671) to Acromelic frontonasal dysostosis (MIM#603671); Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features, MIM#\t617865","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:19:45.024699+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZSWIM6 as ready","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:19:45.020025+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Agree, link to cilia not well established.","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:19:44.978340+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zswim6 has been classified as Amber List (Moderate Evidence).","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:18:19.754831+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZSWIM6 as Amber List (moderate evidence)","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:18:19.743893+10:00","panel_name":"Ciliopathies","panel_id":84,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zswim6 has been classified as Amber List (Moderate Evidence).","entity_name":"ZSWIM6","entity_type":"gene"},{"created":"2020-05-04T20:17:14.731914+10:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ACVR2B were changed from  to Heterotaxy, visceral, 4, autosomal 613751","entity_name":"ACVR2B","entity_type":"gene"},{"created":"2020-05-04T20:16:40.962307+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.2719","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ACVR2B as ready","entity_name":"ACVR2B","entity_type":"gene"}]}