{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=908","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=906","results":[{"created":"2022-03-28T15:55:52.043598+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12148","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CASP10: Rating: GREEN; Mode of pathogenicity: None; Publications: 34329798, 34384744, 20301287; Phenotypes: Autoimmune lymphoproliferative syndrome, type II MIM#603909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"CASP10","entity_type":"gene"},{"created":"2022-03-28T15:55:03.150918+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUBPL as ready","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:55:03.138523+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nubpl has been classified as Green List (High Evidence).","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:50.237204+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.462","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUBPL as ready","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:50.224887+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.462","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nubpl has been classified as Green List (High Evidence).","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:45.415807+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12148","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NUBPL as ready","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:45.403893+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12148","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nubpl has been classified as Green List (High Evidence).","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:43.705335+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4634","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUBPL were changed from  to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:40.670772+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.462","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUBPL were changed from Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242 to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:20.612899+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.462","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUBPL were changed from  to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:54:07.557353+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12148","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NUBPL were changed from  to Mitochondrial complex I deficiency, nuclear type 21 - MIM#618242","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:53:15.074527+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.461","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUBPL were set to ","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:53:00.671993+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12147","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUBPL were set to ","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:52:50.471309+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4633","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NUBPL were set to ","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:52:17.436167+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12146","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:52:12.047602+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.460","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:51:45.944607+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4632","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NUBPL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NUBPL","entity_type":"gene"},{"created":"2022-03-28T15:50:55.372164+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LGI1 as ready","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:50:55.362004+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lgi1 has been classified as Green List (High Evidence).","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:50:52.221133+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1528","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LGI1 were changed from  to Epilepsy, familial temporal lobe, 1, MIM# 6000512","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:50:16.123154+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1527","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LGI1 were set to ","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:49:29.754619+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LGI1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:49:00.562715+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1526","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LGI1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:47:55.319504+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LGI1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18711109, 12205652, 15079010, 22496201; Phenotypes: Epilepsy, familial temporal lobe, 1, MIM# 6000512; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LGI1","entity_type":"gene"},{"created":"2022-03-28T15:45:54.312707+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12145","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTRK1 as ready","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:45:54.299533+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12145","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk1 has been classified as Green List (High Evidence).","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:45:45.536912+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12145","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NTRK1 were changed from  to Insensitivity to pain, congenital, with anhidrosis - MIM#256800","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:44:43.260026+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12144","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NTRK1 were set to ","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:44:04.903302+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12143","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NTRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:43:34.243158+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4631","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTRK1 as ready","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:43:34.232565+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4631","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntrk1 has been classified as Green List (High Evidence).","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:43:28.257657+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4631","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NTRK1 were changed from  to Insensitivity to pain, congenital, with anhidrosis - MIM#256800","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:41:48.108761+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4630","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NTRK1 were set to ","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:41:13.482627+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4629","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NTRK1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:40:43.279799+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4628","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NTRK1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NTRK1","entity_type":"gene"},{"created":"2022-03-28T15:39:46.618363+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12142","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NTF4 as ready","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:39:46.606848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12142","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntf4 has been classified as Red List (Low Evidence).","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:39:38.557683+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12142","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NTF4 were changed from  to Glaucoma 1, open angle, 1O - MIIM#613100","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:39:18.397980+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12141","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NTF4 were set to ","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:38:58.641332+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NTF4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:38:45.692809+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12139","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CASK were changed from FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422 to FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:39.560397+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NTF4 as Red List (low evidence)","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:38:39.550820+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ntf4 has been classified as Red List (Low Evidence).","entity_name":"NTF4","entity_type":"gene"},{"created":"2022-03-28T15:38:31.720589+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12138","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CASK were changed from  to FG syndrome 4 MIM#300422; Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749; Mental retardation, with or without nystagmus MIM#300422","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:14.454775+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12137","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CASK as ready","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:14.446578+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12137","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cask has been classified as Green List (High Evidence).","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:13.849192+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12137","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CASK as ready","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:13.839256+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12137","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cask has been classified as Green List (High Evidence).","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:38:04.856752+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12137","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CASK were set to ","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:37:50.764032+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12136","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CASK was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:37:41.341785+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSUN2 as ready","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:37:41.332437+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsun2 has been classified as Green List (High Evidence).","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:37:32.834220+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSUN2 were changed from  to Mental retardation, autosomal recessive 5 - MIM#611091","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:37:25.517531+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12134","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CASK: Rating: GREEN; Mode of pathogenicity: None; Publications: 24278995; Phenotypes: FG syndrome 4 MIM#300422, Intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia MIM#300749, Mental retardation, with or without nystagmus MIM#300422; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males); Current diagnostic: yes","entity_name":"CASK","entity_type":"gene"},{"created":"2022-03-28T15:37:11.896156+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12134","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSUN2 were set to ","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:36:48.332744+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12133","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSUN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:34:05.940134+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12132","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSUN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 22541559, 22541562, 21063731, 22577224, 35126837; Phenotypes: Mental retardation, autosomal recessive 5 - MIM#611091; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:32:46.006671+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4627","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSUN2 as ready","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:32:45.988567+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4627","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsun2 has been classified as Green List (High Evidence).","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:32:38.252589+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4627","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NSUN2 were changed from  to Mental retardation, autosomal recessive 5 - MIM#611091","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:31:46.752237+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4626","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NSUN2 were set to ","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:31:07.323354+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4625","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NSUN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:30:34.258568+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4624","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSUN2: Rating: GREEN; Mode of pathogenicity: None; Publications: 35126837; Phenotypes: Mental retardation, autosomal recessive 5 - MIM#611091; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"NSUN2","entity_type":"gene"},{"created":"2022-03-28T15:27:08.647107+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12132","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRXN1 as ready","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:27:08.635492+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nrxn1 has been classified as Green List (High Evidence).","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:26:51.656881+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12132","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRXN1 were changed from  to Pitt-Hopkins-like syndrome 2 - MIM#614325","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:26:23.751363+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12131","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NRXN1 were set to ","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:26:05.023688+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12130","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:25:34.997557+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.183","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRXN1 as ready","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:25:34.985186+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.183","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nrxn1 has been classified as Green List (High Evidence).","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:24:37.960081+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12129","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CARD11 were changed from Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638 to Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:24:18.676387+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.183","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRXN1 were changed from  to Pitt-Hopkins-like syndrome 2 - MIM#614325","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:24:10.816990+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12128","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CARD11 were changed from  to Immunodeficiency 11A, autosomal recessive, MIM# 615206; Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:24:10.060922+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12128","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CARD11 as ready","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:24:10.050564+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12128","user_name":"Ain Roesley","item_type":"entity","text":"Gene: card11 has been classified as Green List (High Evidence).","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:24:02.439709+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12128","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CARD11 were set to ","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:23:49.085670+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.182","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NRXN1 were set to ","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:23:38.436352+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12128","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CARD11 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:23:18.706586+11:00","panel_name":"Autism","panel_id":51,"panel_version":"0.181","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:23:11.948328+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.332","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CACNA2D2 as ready","entity_name":"CACNA2D2","entity_type":"gene"},{"created":"2022-03-28T15:23:11.904620+11:00","panel_name":"Ataxia - paediatric","panel_id":271,"panel_version":"0.332","user_name":"Ain Roesley","item_type":"entity","text":"Gene: cacna2d2 has been classified as Green List (High Evidence).","entity_name":"CACNA2D2","entity_type":"gene"},{"created":"2022-03-28T15:23:08.799581+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CARD11: Rating: GREEN; Mode of pathogenicity: None; Publications: 23561803, 12818158, 23374270, 28628108; Phenotypes: Immunodeficiency 11A, autosomal recessive, MIM# 615206, Immunodeficiency 11B with atopic dermatitis, autosomal dominant, MIM# 617638; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"CARD11","entity_type":"gene"},{"created":"2022-03-28T15:22:39.256988+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRXN1 were changed from Pitt-Hopkins-like syndrome 2 - MIM#614325 to Pitt-Hopkins-like syndrome 2 - MIM#614325","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:22:37.301882+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRXN1 as ready","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:22:37.290407+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nrxn1 has been classified as Green List (High Evidence).","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:22:06.679437+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1525","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRXN1 were changed from  to Pitt-Hopkins-like syndrome 2 - MIM#614325","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:21:44.981593+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CALM3 as ready","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:21:44.967550+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"Gene: calm3 has been classified as Green List (High Evidence).","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:21:31.859757+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"Phenotypes for gene: CALM3 were changed from  to Long QT syndrome 16 MIM#618782; CPVT","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:21:19.654016+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"Publications for gene: CALM3 were set to ","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:21:16.386895+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12127","user_name":"Ain Roesley","item_type":"entity","text":"Mode of inheritance for gene: CALM3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:21:10.337709+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1524","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NRXN1 were set to ","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:20:53.130901+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12126","user_name":"Ain Roesley","item_type":"entity","text":"reviewed gene: CALM3: Rating: GREEN; Mode of pathogenicity: None; Publications: 31983240; Phenotypes: Long QT syndrome 16 MIM#618782, CPVT; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes","entity_name":"CALM3","entity_type":"gene"},{"created":"2022-03-28T15:20:29.280753+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1523","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NRXN1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:19:56.267183+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1522","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NRXN1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:19:20.302338+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12126","user_name":"Ain Roesley","item_type":"entity","text":"Marked gene: CALM2 as ready","entity_name":"CALM2","entity_type":"gene"},{"created":"2022-03-28T15:19:20.289015+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12126","user_name":"Ain Roesley","item_type":"entity","text":"Gene: calm2 has been classified as Green List (High Evidence).","entity_name":"CALM2","entity_type":"gene"},{"created":"2022-03-28T15:18:56.061855+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4624","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NRXN1 as ready","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:18:56.052366+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4624","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nrxn1 has been classified as Green List (High Evidence).","entity_name":"NRXN1","entity_type":"gene"},{"created":"2022-03-28T15:18:51.386300+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4624","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NRXN1 were changed from  to Pitt-Hopkins-like syndrome 2 - MIM#614325","entity_name":"NRXN1","entity_type":"gene"}]}