{"count":220363,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=935","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=933","results":[{"created":"2022-03-16T18:28:31.775470+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11456","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndst1 has been classified as Green List (High Evidence).","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:28:22.975235+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11456","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDST1 were changed from  to Mental retardation, autosomal recessive 46 - MIM#616116","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:27:52.548629+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11455","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDST1 were set to ","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:27:28.044324+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11454","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDST1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:25:42.304874+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4575","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDST1 as ready","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:25:42.294128+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4575","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndst1 has been classified as Green List (High Evidence).","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:25:23.616145+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4575","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NDST1 were changed from  to Mental retardation, autosomal recessive 46 - MIM#616116","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:24:48.881654+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4574","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NDST1 were set to ","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:24:03.584073+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4573","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NDST1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:23:18.203064+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NDST1 as ready","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:23:18.193461+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndst1 has been classified as Green List (High Evidence).","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:23:15.087955+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDST1 as Green List (high evidence)","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:23:15.078608+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1483","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndst1 has been classified as Green List (High Evidence).","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:21:41.932155+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1482","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NDST1 as Green List (high evidence)","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:21:41.922359+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"0.1482","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ndst1 has been classified as Green List (High Evidence).","entity_name":"NDST1","entity_type":"gene"},{"created":"2022-03-16T18:20:08.983640+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11453","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCR3 as ready","entity_name":"NCR3","entity_type":"gene"},{"created":"2022-03-16T18:20:08.972552+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11453","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncr3 has been classified as Red List (Low Evidence).","entity_name":"NCR3","entity_type":"gene"},{"created":"2022-03-16T18:19:59.031123+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11453","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NCR3 as Red List (low evidence)","entity_name":"NCR3","entity_type":"gene"},{"created":"2022-03-16T18:19:59.021984+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11453","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncr3 has been classified as Red List (Low Evidence).","entity_name":"NCR3","entity_type":"gene"},{"created":"2022-03-16T18:18:53.649605+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11452","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCOA4 as ready","entity_name":"NCOA4","entity_type":"gene"},{"created":"2022-03-16T18:18:53.638458+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11452","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncoa4 has been classified as Red List (Low Evidence).","entity_name":"NCOA4","entity_type":"gene"},{"created":"2022-03-16T18:18:43.775293+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11452","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NCOA4 as Red List (low evidence)","entity_name":"NCOA4","entity_type":"gene"},{"created":"2022-03-16T18:18:43.764585+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11452","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncoa4 has been classified as Red List (Low Evidence).","entity_name":"NCOA4","entity_type":"gene"},{"created":"2022-03-16T17:21:21.969772+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11451","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCF4 as ready","entity_name":"NCF4","entity_type":"gene"},{"created":"2022-03-16T17:21:21.959477+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11451","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncf4 has been classified as Green List (High Evidence).","entity_name":"NCF4","entity_type":"gene"},{"created":"2022-03-16T17:20:31.071812+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11451","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCF4 were changed from  to Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960","entity_name":"NCF4","entity_type":"gene"},{"created":"2022-03-16T17:20:08.878797+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11450","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCF4 were set to ","entity_name":"NCF4","entity_type":"gene"},{"created":"2022-03-16T17:19:45.839244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11449","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCF4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCF4","entity_type":"gene"},{"created":"2022-03-16T17:15:16.606521+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCF2 as ready","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T17:15:16.588205+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncf2 has been classified as Green List (High Evidence).","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T17:11:30.344558+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCF2 were changed from  to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T17:10:56.199765+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCF2 were set to ","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T17:07:40.416266+11:00","panel_name":"Inflammatory bowel disease","panel_id":123,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:56:14.876261+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11448","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NCF2 as ready","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:56:14.865263+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11448","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ncf2 has been classified as Green List (High Evidence).","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:54:30.807256+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11448","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: NCF2 were changed from  to Chronic granulomatous disease 2, autosomal recessive, MIM# 233710","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:54:08.975819+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11447","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: NCF2 were set to ","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:53:48.867345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11446","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: NCF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"NCF2","entity_type":"gene"},{"created":"2022-03-16T16:52:48.731957+11:00","panel_name":"Amelogenesis imperfecta","panel_id":3564,"panel_version":"1.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DSPP as ready","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-03-16T16:52:48.721305+11:00","panel_name":"Amelogenesis imperfecta","panel_id":3564,"panel_version":"1.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dspp has been classified as Green List (High Evidence).","entity_name":"DSPP","entity_type":"gene"},{"created":"2022-03-16T16:52:08.184067+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11445","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SALL4 as ready","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:52:08.171174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11445","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sall4 has been classified as Green List (High Evidence).","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:51:58.363904+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11445","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SALL4 were changed from  to Duane-radial ray syndrome, MIM# 607323; MONDO:0011812; IVIC syndrome, MIM# 147750; MONDO:0007836","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:51:35.926069+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11444","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SALL4 were set to ","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:44:44.702209+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11443","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SALL4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:44:22.019411+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11442","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SALL4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Duane-radial ray syndrome, MIM# 607323, MONDO:0011812, IVIC syndrome, MIM# 147750, MONDO:0007836; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SALL4","entity_type":"gene"},{"created":"2022-03-16T16:39:14.890077+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11442","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TYROBP as ready","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:39:14.879632+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11442","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tyrobp has been classified as Green List (High Evidence).","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:38:59.884781+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11442","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TYROBP were changed from  to Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, MIM# 221770","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:38:29.868655+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11441","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TYROBP were set to ","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:37:36.665131+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11440","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TYROBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:37:12.785333+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11439","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TYROBP: Rating: GREEN; Mode of pathogenicity: None; Publications: 10888890, 12370476, 27904822; Phenotypes: Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1, MIM# 221770; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TYROBP","entity_type":"gene"},{"created":"2022-03-16T16:32:08.316336+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRAK4 as ready","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:32:08.306275+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irak4 has been classified as Green List (High Evidence).","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:30:26.985361+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRAK4 were changed from  to Immunodeficiency 67, MIM# 607676","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:29:48.231029+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRAK4 were set to ","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:29:18.503365+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IRAK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:28:47.373451+11:00","panel_name":"Defects of innate immunity","panel_id":231,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRAK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26825884, 17878374, 17544092, 16950813; Phenotypes: Immunodeficiency 67, MIM# 607676; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:28:00.964830+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11439","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IRAK4 as ready","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:28:00.951680+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11439","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: irak4 has been classified as Green List (High Evidence).","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:27:52.422213+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11439","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IRAK4 were changed from  to Immunodeficiency 67, MIM# 607676","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:27:29.913964+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11438","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IRAK4 were set to ","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:26:44.186387+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11437","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IRAK4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:26:25.971277+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11436","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IRAK4: Rating: GREEN; Mode of pathogenicity: None; Publications: 26825884, 17878374, 17544092, 16950813; Phenotypes: Immunodeficiency 67, MIM# 607676; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"IRAK4","entity_type":"gene"},{"created":"2022-03-16T16:24:40.551625+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11436","user_name":"Manny Jacobs","item_type":"entity","text":"reviewed gene: TYK2: Rating: GREEN; Mode of pathogenicity: None; Publications: 17088085, 17521577, 26304966; Phenotypes: # 611521 IMMUNODEFICIENCY 35; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TYK2","entity_type":"gene"},{"created":"2022-03-16T16:23:22.261378+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11436","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INSR as ready","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:23:22.247243+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11436","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insr has been classified as Green List (High Evidence).","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:22:36.397195+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11436","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INSR were changed from  to Hyperinsulinemic hypoglycemia, familial, 5, MIM# 609968; Leprechaunism, MIM# 246200; Rabson-Mendenhall syndrome, MIM# 262190","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:22:15.223541+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11435","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INSR were set to ","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:21:56.530601+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11434","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INSR was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:21:35.700493+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11433","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INSR: Rating: GREEN; Mode of pathogenicity: None; Publications: 34965699; Phenotypes: Hyperinsulinemic hypoglycemia, familial, 5, MIM# 609968, Leprechaunism, MIM# 246200, Rabson-Mendenhall syndrome, MIM# 262190; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"INSR","entity_type":"gene"},{"created":"2022-03-16T16:17:54.326718+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11433","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INS as ready","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:17:54.316517+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11433","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ins has been classified as Green List (High Evidence).","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:17:40.134945+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11433","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INS were changed from  to Diabetes mellitus, insulin-dependent, 2, MIM# 125852; Diabetes mellitus, permanent neonatal 4, MIM# 618858; Maturity-onset diabetes of the young, type 10, MIM# 613370","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:17:17.617111+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11432","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INS were set to ","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:16:55.622731+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11431","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INS was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:16:37.186488+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11430","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INS: Rating: GREEN; Mode of pathogenicity: None; Publications: 18162506; Phenotypes: Diabetes mellitus, insulin-dependent, 2, MIM# 125852, Diabetes mellitus, permanent neonatal 4, MIM# 618858, Maturity-onset diabetes of the young, type 10, MIM# 613370; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"INS","entity_type":"gene"},{"created":"2022-03-16T16:14:08.784277+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INO80 as ready","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:14:08.772710+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ino80 has been classified as Amber List (Moderate Evidence).","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:13:58.036083+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INO80 were changed from  to Primary immunodeficiency, MONDO:0003778","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:13:28.745043+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INO80 were set to ","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:12:49.530355+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INO80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:10:03.355866+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INO80 as Amber List (moderate evidence)","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:10:03.341836+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ino80 has been classified as Amber List (Moderate Evidence).","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:09:02.390766+11:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INO80: Rating: AMBER; Mode of pathogenicity: None; Publications: 25312759; Phenotypes: Primary immunodeficiency, MONDO:0003778; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:08:39.572351+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11430","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INO80 as ready","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:08:39.562392+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11430","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ino80 has been classified as Amber List (Moderate Evidence).","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:08:25.784066+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11430","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INO80 were changed from  to Primary immunodeficiency, MONDO:0003778","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:08:00.529250+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11429","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INO80 were set to ","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:07:39.052860+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11428","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INO80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:07:20.535100+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11427","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INO80 as Amber List (moderate evidence)","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:07:20.523640+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11427","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ino80 has been classified as Amber List (Moderate Evidence).","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:07:17.361803+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11426","user_name":"Manny Jacobs","item_type":"entity","text":"reviewed gene: TYMP: Rating: GREEN; Mode of pathogenicity: None; Publications: 21933806; Phenotypes: # 603041 MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TYMP","entity_type":"gene"},{"created":"2022-03-16T16:06:56.549791+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11426","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INO80: Rating: AMBER; Mode of pathogenicity: None; Publications: 25312759; Phenotypes: Primary immunodeficiency, MONDO:0003778; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"INO80","entity_type":"gene"},{"created":"2022-03-16T16:02:29.657327+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11426","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IMPAD1 as ready","entity_name":"IMPAD1","entity_type":"gene"},{"created":"2022-03-16T16:02:29.647611+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11426","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: impad1 has been classified as Green List (High Evidence).","entity_name":"IMPAD1","entity_type":"gene"},{"created":"2022-03-16T16:02:12.409327+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11426","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IMPAD1 were changed from  to Chondrodysplasia with joint dislocations, GPAPP type MIM#614078","entity_name":"IMPAD1","entity_type":"gene"},{"created":"2022-03-16T16:01:45.137245+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11425","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IMPAD1 were set to ","entity_name":"IMPAD1","entity_type":"gene"},{"created":"2022-03-16T16:01:24.343186+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11424","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IMPAD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"IMPAD1","entity_type":"gene"},{"created":"2022-03-16T16:01:02.161695+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.11423","user_name":"Zornitza Stark","item_type":"entity","text":"Deleted their review","entity_name":"IMPAD1","entity_type":"gene"}]}