{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=881","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=879","results":[{"created":"2022-04-18T11:25:38.200648+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13004","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkcg has been classified as Green List (High Evidence).","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:25:33.865738+10:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKCG as ready","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:25:33.854107+10:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkcg has been classified as Amber List (Moderate Evidence).","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:25:28.954875+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKCG as ready","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:25:28.925372+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkcg has been classified as Red List (Low Evidence).","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:25:10.738647+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.469","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKCG were changed from  to Spinocerebellar ataxia 14, MIM# 605361","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:24:41.245297+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.468","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRKCG were set to ","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:24:18.649070+10:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRKCG as Amber List (moderate evidence)","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:24:18.639268+10:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.334","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkcg has been classified as Amber List (Moderate Evidence).","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:24:08.724971+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13004","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKCG were changed from  to Spinocerebellar ataxia 14, MIM# 605361","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:24:05.680527+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.467","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKCG was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:23:37.186267+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.466","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRKCG as Red List (low evidence)","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:23:37.173397+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.466","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkcg has been classified as Red List (Low Evidence).","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:23:15.053067+10:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.333","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PRKCG was added\ngene: PRKCG was added to Ataxia - paediatric. Sources: Expert Review\nMode of inheritance for gene: PRKCG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: PRKCG were set to 34292398\nPhenotypes for gene: PRKCG were set to Spinocerebellar ataxia 14, MIM# 605361\nReview for gene: PRKCG was set to AMBER\nAdded comment: Typically adult onset, but note two individuals reported with severe paediatric onset. \nSources: Expert Review","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:22:42.012382+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13003","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRKCG were set to ","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:22:21.817133+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13002","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKCG was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:21:29.626468+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1561","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRMT7 as ready","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:21:29.613127+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1561","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prmt7 has been classified as Green List (High Evidence).","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:21:26.043408+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1561","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRMT7 were changed from  to Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:20:43.257890+10:00","panel_name":"Regression","panel_id":206,"panel_version":"0.465","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRKCG: Rating: RED; Mode of pathogenicity: None; Publications: 12644968, 14676051, 14694043, 16193476, 33739604, 34292398; Phenotypes: Spinocerebellar ataxia 14, MIM# 605361; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:19:43.305136+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13001","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRKCG: Rating: GREEN; Mode of pathogenicity: None; Publications: 12644968, 14676051, 14694043, 16193476, 33739604, 34292398; Phenotypes: Spinocerebellar ataxia 14, MIM# 605361; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKCG","entity_type":"gene"},{"created":"2022-04-18T11:16:32.586747+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1560","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRMT7 were set to ","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:14:49.062056+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13001","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKG1 as ready","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:14:49.049586+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13001","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkg1 has been classified as Green List (High Evidence).","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:14:35.705367+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13001","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKG1 were changed from  to Aortic aneurysm, familial thoracic 8, MIM# 615436","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:14:12.717662+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.13000","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRKG1 were set to ","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:13:51.947902+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12999","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:13:32.184925+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12998","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRKG1: Rating: GREEN; Mode of pathogenicity: None; Publications: 30071989, 23910461, 30577811; Phenotypes: Aortic aneurysm, familial thoracic 8, MIM# 615436; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKG1","entity_type":"gene"},{"created":"2022-04-18T11:11:48.486927+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1559","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRMT7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:11:10.906366+10:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1558","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRMT7: Rating: GREEN; Mode of pathogenicity: None; Publications: 26437029, 27718516, 30513135; Phenotypes: Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:10:32.988694+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4680","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRMT7 as ready","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:10:32.977723+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4680","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prmt7 has been classified as Green List (High Evidence).","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:10:27.920846+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4680","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRMT7 were changed from  to Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:10:00.418349+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12998","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRMT7 as ready","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:10:00.396142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12998","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prmt7 has been classified as Green List (High Evidence).","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:09:53.445608+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4679","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRMT7 were set to ","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:09:51.208031+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12998","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRMT7 were changed from  to Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:09:30.949736+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12997","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRMT7 were set to ","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:09:18.718274+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4678","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRMT7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:08:51.335885+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12996","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRMT7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:08:35.462880+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4677","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRMT7: Rating: GREEN; Mode of pathogenicity: None; Publications: 26437029, 27718516, 30513135; Phenotypes: Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:07:50.104204+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12995","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRMT7: Rating: GREEN; Mode of pathogenicity: None; Publications: 26437029, 27718516, 30513135; Phenotypes: Short stature, brachydactyly, intellectual developmental disability, and seizures, MIM# 617157; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRMT7","entity_type":"gene"},{"created":"2022-04-18T11:06:11.051071+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12995","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRODH as ready","entity_name":"PRODH","entity_type":"gene"},{"created":"2022-04-18T11:06:11.041781+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12995","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prodh has been classified as Green List (High Evidence).","entity_name":"PRODH","entity_type":"gene"},{"created":"2022-04-18T11:05:50.605364+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12995","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRODH were changed from  to Hyperprolinaemia, type I 239500; Proline oxidase deficiency","entity_name":"PRODH","entity_type":"gene"},{"created":"2022-04-18T11:05:28.338395+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12994","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRODH were set to ","entity_name":"PRODH","entity_type":"gene"},{"created":"2022-04-18T11:05:05.723543+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12993","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRODH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRODH","entity_type":"gene"},{"created":"2022-04-18T11:03:59.038842+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12992","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROK2 as ready","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:03:59.027084+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12992","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prok2 has been classified as Green List (High Evidence).","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:03:41.063074+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROK2 as ready","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:03:41.049725+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prok2 has been classified as Red List (Low Evidence).","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:03:35.104102+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.435","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PROK2 were changed from  to Hypogonadotropic hypogonadism 4 with or without anosmia, MIM# 610628","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:03:01.595311+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.434","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PROK2 were set to ","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:02:24.853765+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.433","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PROK2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:01:56.278254+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PROK2 as Red List (low evidence)","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:01:56.267899+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.432","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prok2 has been classified as Red List (Low Evidence).","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:01:21.679017+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.431","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PROK2: Rating: RED; Mode of pathogenicity: None; Publications: 18559922, 17054399, 17959774, 18285834; Phenotypes: Hypogonadotropic hypogonadism 4 with or without anosmia, MIM# 610628; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T11:00:10.824659+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12992","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PROK2 were changed from  to Hypogonadotropic hypogonadism 4 with or without anosmia, MIM# 610628","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T10:59:14.403546+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12991","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PROK2 were set to ","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T10:58:36.650813+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12990","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PROK2 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T10:58:16.368077+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12989","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PROK2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18559922, 17054399, 17959774, 18285834; Phenotypes: Hypogonadotropic hypogonadism 4 with or without anosmia, MIM# 610628; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROK2","entity_type":"gene"},{"created":"2022-04-18T10:54:56.593539+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12989","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROM1 as ready","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-18T10:54:56.584431+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12989","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prom1 has been classified as Green List (High Evidence).","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-18T10:54:35.314296+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12989","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PROM1 were changed from  to Inherited retinal dystrophy, MONDO:0019118; Cone-rod dystrophy 12, MIM# 612657; Macular dystrophy, retinal, 2, MI# 608051; Retinitis pigmentosa 41, MIM# 612095; Stargardt disease 4, MIM# 603786","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-18T10:53:56.369362+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12988","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PROM1 were set to ","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-18T10:53:34.884473+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12987","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PROM1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-18T10:53:14.089116+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12986","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PROM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 10587575, 17605048, 18654668, 29416601, 31576780, 34664634, 32820593; Phenotypes: Inherited retinal dystrophy, MONDO:0019118, Cone-rod dystrophy 12, MIM# 612657, Macular dystrophy, retinal, 2, MI# 608051, Retinitis pigmentosa 41, MIM# 612095, Stargardt disease 4, MIM# 603786; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROM1","entity_type":"gene"},{"created":"2022-04-16T16:00:38.243475+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12986","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PROS1 as ready","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T16:00:38.231551+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12986","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pros1 has been classified as Green List (High Evidence).","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T16:00:28.920845+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12986","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PROS1 were changed from  to Thrombophilia 5 due to protein S deficiency, autosomal dominant, MIM# 612336; Thrombophilia 5 due to protein S deficiency, autosomal recessive, MIM# 614514","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T16:00:07.371536+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12985","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PROS1 were set to ","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T15:59:46.455896+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12984","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PROS1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T15:59:26.812109+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12983","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PROS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 7545463, 19466456, 10063989, 20484936, 19729839; Phenotypes: Thrombophilia 5 due to protein S deficiency, autosomal dominant, MIM# 612336, Thrombophilia 5 due to protein S deficiency, autosomal recessive, MIM# 614514; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"PROS1","entity_type":"gene"},{"created":"2022-04-16T15:55:07.406078+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12983","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRPF3 as ready","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:55:07.389608+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12983","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prpf3 has been classified as Green List (High Evidence).","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:54:42.456518+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12983","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRPF3 were changed from  to Retinitis pigmentosa 18, MIM# 601414","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:54:27.430866+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12982","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRPF3 were set to ","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:54:06.175923+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12981","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRPF3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:53:45.340131+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12980","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRPF3: Rating: GREEN; Mode of pathogenicity: None; Publications: 11773002, 27886254; Phenotypes: Retinitis pigmentosa 18, MIM# 601414; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF3","entity_type":"gene"},{"created":"2022-04-16T15:50:19.754164+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12980","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRPF4 as ready","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:50:19.741867+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12980","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prpf4 has been classified as Green List (High Evidence).","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:50:09.966802+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12980","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRPF4 were changed from  to Retinitis pigmentosa 70, MIM# 615922","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:49:46.837270+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12979","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRPF4 were set to ","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:49:23.537775+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12978","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRPF4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:48:25.424306+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12977","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRPF4: Rating: GREEN; Mode of pathogenicity: None; Publications: 24419317, 25383878; Phenotypes: Retinitis pigmentosa 70, MIM# 615922; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF4","entity_type":"gene"},{"created":"2022-04-16T15:44:48.203151+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12977","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRPF6 as ready","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:44:48.177671+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12977","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prpf6 has been classified as Amber List (Moderate Evidence).","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:44:35.385363+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12977","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRPF6 were changed from  to Retinitis pigmentosa 60, MIM# 613983","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:43:59.912351+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12976","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRPF6 were set to ","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:43:37.585301+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12975","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRPF6 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:43:15.106559+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12974","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PRPF6 as Amber List (moderate evidence)","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:43:15.091717+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12974","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prpf6 has been classified as Amber List (Moderate Evidence).","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:42:39.755172+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12973","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRPF6: Rating: AMBER; Mode of pathogenicity: None; Publications: 21549338, 32335390; Phenotypes: Retinitis pigmentosa 60, MIM# 613983; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRPF6","entity_type":"gene"},{"created":"2022-04-16T15:37:28.790223+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRPH as ready","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:37:28.770753+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prph has been classified as Amber List (Moderate Evidence).","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:37:21.629545+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRPH were changed from  to {Amyotrophic lateral sclerosis, susceptibility to}, 105400","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:36:39.887598+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12973","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRPH as ready","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:36:39.875146+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12973","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prph has been classified as Amber List (Moderate Evidence).","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:36:30.413559+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12973","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRPH were changed from  to {Amyotrophic lateral sclerosis, susceptibility to}, 105400","entity_name":"PRPH","entity_type":"gene"},{"created":"2022-04-16T15:36:30.014251+10:00","panel_name":"Motor Neurone Disease","panel_id":25,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRPH were set to ","entity_name":"PRPH","entity_type":"gene"}]}