{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1725","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1723","results":[{"created":"2020-07-18T20:18:36.253896+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: NSMF as Red List (low evidence)","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:18:36.243750+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsmf has been classified as Red List (Low Evidence).","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:18:09.892306+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: NSMF: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypogonadotropic hypogonadism 9 with or without anosmia, MIM# 614838; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:17:20.796856+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: NSMF as ready","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:17:20.789915+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: nsmf has been classified as Red List (Low Evidence).","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:17:12.916201+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.157","user_name":"Zornitza Stark","item_type":"entity","text":"gene: NSMF was added\ngene: NSMF was added to Disorders of Sex Differentiation. Sources: Expert list\nMode of inheritance for gene: NSMF was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: NSMF were set to 15362570; 17235395; 21700882\nPhenotypes for gene: NSMF were set to Hypogonadotropic hypogonadism 9 with or without anosmia, MIM#\t614838\nReview for gene: NSMF was set to RED\nAdded comment: Rare variants reported in individuals with IHH; however, variants in other IHH genes also present, and at least one of the variants has a very high population frequency in gnomad (intronic 8-bp deletion ending 14 bp before exon 10 (1159-14_-22del), present in 258 individuals). \nSources: Expert list","entity_name":"NSMF","entity_type":"gene"},{"created":"2020-07-18T20:10:07.960870+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: SPRY4.","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:59.408909+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3408","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPRY4 as ready","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:59.402471+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3408","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Amber List (Moderate Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:52.207075+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3408","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: SPRY4.","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:40.548277+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3408","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SPRY4 were changed from  to Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:23.914014+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3407","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SPRY4 were set to ","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:09:08.867199+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3406","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SPRY4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:08:49.485769+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3405","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPRY4 as Amber List (moderate evidence)","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:08:49.475428+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3405","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Amber List (Moderate Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:08:33.845016+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3404","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SPRY4: Rating: AMBER; Mode of pathogenicity: None; Publications: 23643382; Phenotypes: Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:07:37.836492+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPRY4 as ready","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:07:37.829073+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Red List (Low Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:07:35.000160+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SPRY4 were changed from  to Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:07:10.730906+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SPRY4 were set to ","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:06:48.663545+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SPRY4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:06:28.020985+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPRY4 as Red List (low evidence)","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:06:28.011608+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Red List (Low Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:06:04.146761+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SPRY4: Rating: RED; Mode of pathogenicity: None; Publications: 23643382; Phenotypes: Hypogonadotropic hypogonadism 17 with or without anosmia, MIM# 615266; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:05:09.157364+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SPRY4 as ready","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:05:09.147464+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Amber List (Moderate Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:05:04.650516+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SPRY4 as Amber List (moderate evidence)","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:05:04.641256+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.156","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: spry4 has been classified as Amber List (Moderate Evidence).","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T20:04:41.031969+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.155","user_name":"Zornitza Stark","item_type":"entity","text":"gene: SPRY4 was added\ngene: SPRY4 was added to Disorders of Sex Differentiation. Sources: Expert list\nMode of inheritance for gene: SPRY4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: SPRY4 were set to 23643382\nPhenotypes for gene: SPRY4 were set to Hypogonadotropic hypogonadism 17 with or without anosmia, MIM#\t615266\nReview for gene: SPRY4 was set to AMBER\nAdded comment: 14 unrelated individuals reported originally. Three of these had variants in other IHH genes. The p.Lys177Arg variant is present in 454 individuals in gnomad, p.Ser241Tyr is present in 1279 individuals including 6 homozygotes, p.Val304Ile is present in 457 individuals. These population frequencies cast doubt on the gene-disease relationship. \nSources: Expert list","entity_name":"SPRY4","entity_type":"gene"},{"created":"2020-07-18T19:57:58.051207+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3404","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KISS1 as ready","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:57:58.042055+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3404","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Amber List (Moderate Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:57:51.509625+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3404","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KISS1 were changed from  to Hypogonadotropic hypogonadism 13 with or without anosmia, MIM# 614842","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:57:33.709784+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3403","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KISS1 were set to ","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:57:16.667281+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3402","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KISS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:56:59.916909+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3401","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KISS1 as Amber List (moderate evidence)","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:56:59.907496+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3401","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Amber List (Moderate Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:56:44.637871+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3400","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KISS1: Rating: AMBER; Mode of pathogenicity: None; Publications: 22335740, 25783047, 22766261, 17563351; Phenotypes: Hypogonadotropic hypogonadism 13 with or without anosmia, MIM# 614842; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:55:50.474866+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KISS1 as ready","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:55:50.466421+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Red List (Low Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:55:47.261854+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.165","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KISS1 were changed from  to Hypogonadotropic hypogonadism 13 with or without anosmia, MIM# 614842","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:55:25.840655+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.164","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KISS1 were set to ","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:55:03.829507+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KISS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:54:43.044153+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KISS1 as Red List (low evidence)","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:54:43.037942+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Red List (Low Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:54:19.373834+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KISS1: Rating: RED; Mode of pathogenicity: None; Publications: 22335740, 25783047, 22766261, 17563351; Phenotypes: Hypogonadotropic hypogonadism 13 with or without anosmia, MIM# 614842; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:53:29.532327+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KISS1 as ready","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:53:29.522487+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Amber List (Moderate Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:53:15.364415+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KISS1 as Amber List (moderate evidence)","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:53:15.357209+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.154","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kiss1 has been classified as Amber List (Moderate Evidence).","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:52:50.453892+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.153","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KISS1 was added\ngene: KISS1 was added to Disorders of Sex Differentiation. Sources: Expert list\nMode of inheritance for gene: KISS1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KISS1 were set to 22335740; 25783047; 22766261; 17563351\nPhenotypes for gene: KISS1 were set to Hypogonadotropic hypogonadism 13 with or without anosmia, MIM#\t614842\nReview for gene: KISS1 was set to AMBER\nAdded comment: Reported in Turkish families, supportive mouse model, but no variants identified in other cohorts. Role of KISS1 receptor much more established. \nSources: Expert list","entity_name":"KISS1","entity_type":"gene"},{"created":"2020-07-18T19:42:35.914019+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TACR3 as ready","entity_name":"TACR3","entity_type":"gene"},{"created":"2020-07-18T19:42:35.903591+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tacr3 has been classified as Green List (High Evidence).","entity_name":"TACR3","entity_type":"gene"},{"created":"2020-07-18T19:42:31.870382+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TACR3 as Green List (high evidence)","entity_name":"TACR3","entity_type":"gene"},{"created":"2020-07-18T19:42:31.860790+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.152","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tacr3 has been classified as Green List (High Evidence).","entity_name":"TACR3","entity_type":"gene"},{"created":"2020-07-18T19:42:08.368415+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.151","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TACR3 was added\ngene: TACR3 was added to Disorders of Sex Differentiation. Sources: Expert list\nMode of inheritance for gene: TACR3 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: TACR3 were set to 20332248; 19079066\nPhenotypes for gene: TACR3 were set to Hypogonadotropic hypogonadism 11 with or without anosmia, MIM#\t614840\nReview for gene: TACR3 was set to GREEN\nAdded comment: Multiple families reported. \nSources: Expert list","entity_name":"TACR3","entity_type":"gene"},{"created":"2020-07-18T18:15:58.189217+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3400","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INSL3 as ready","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:58.181708+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3400","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insl3 has been classified as Amber List (Moderate Evidence).","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:51.926533+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3400","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INSL3 were changed from  to Cryptorchidism, MIM# 219050","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:35.508322+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3399","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INSL3 were set to ","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:19.642696+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3398","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INSL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:04.605272+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3397","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INSL3 as Amber List (moderate evidence)","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:15:04.598517+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3397","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insl3 has been classified as Amber List (Moderate Evidence).","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:14:47.302508+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3396","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INSL3: Rating: AMBER; Mode of pathogenicity: None; Publications: 12601553, 12970298, 11095425; Phenotypes: Cryptorchidism, MIM# 219050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:13:59.084687+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: INSL3 as ready","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:13:59.075808+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insl3 has been classified as Amber List (Moderate Evidence).","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:13:56.721848+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.150","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: INSL3 were changed from  to Cryptorchidism, MIM# 219050","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:13:35.743434+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.149","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: INSL3 were set to ","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:13:15.093279+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.148","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: INSL3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:12:54.333108+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: INSL3 as Amber List (moderate evidence)","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:12:54.326726+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.147","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: insl3 has been classified as Amber List (Moderate Evidence).","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:12:32.562396+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: INSL3: Rating: AMBER; Mode of pathogenicity: None; Publications: 12601553, 12970298, 11095425; Phenotypes: Cryptorchidism, MIM# 219050; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"INSL3","entity_type":"gene"},{"created":"2020-07-18T18:08:44.538024+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL17RD as ready","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:08:44.528448+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Red List (Low Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:08:42.328146+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL17RD were changed from  to Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:08:19.767091+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL17RD as Red List (low evidence)","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:08:19.760623+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.160","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Red List (Low Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:07:57.730783+10:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.159","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL17RD: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267; Mode of inheritance: None","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:07:30.702603+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3396","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL17RD as ready","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:07:30.690142+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3396","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Amber List (Moderate Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:07:23.580987+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3396","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL17RD were changed from  to Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:07:06.423570+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3395","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL17RD were set to ","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:06:50.266859+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3394","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL17RD was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:06:36.051898+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3393","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL17RD as Amber List (moderate evidence)","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:06:36.044543+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3393","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Amber List (Moderate Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:06:18.052765+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3392","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL17RD: Rating: AMBER; Mode of pathogenicity: None; Publications: 23643382, 32389901; Phenotypes: Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:05:05.170813+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Tag disputed tag was added to gene: IL17RD.","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:04:58.824554+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: IL17RD as ready","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:04:58.817740+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Amber List (Moderate Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:04:49.754002+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.146","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: IL17RD were changed from  to Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:04:10.026590+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.145","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: IL17RD were set to ","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:03:53.508441+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.144","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: IL17RD was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:03:35.963902+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: IL17RD as Amber List (moderate evidence)","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:03:35.954358+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.143","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: il17rd has been classified as Amber List (Moderate Evidence).","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:02:34.056117+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: IL17RD: Changed rating: AMBER","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T18:02:24.460712+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: IL17RD: Rating: GREEN; Mode of pathogenicity: None; Publications: 23643382, 32389901; Phenotypes: Hypogonadotropic hypogonadism 18 with or without anosmia, MIM# 615267; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"IL17RD","entity_type":"gene"},{"created":"2020-07-18T17:49:33.448877+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HSD17B4 as ready","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2020-07-18T17:49:33.442138+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hsd17b4 has been classified as Green List (High Evidence).","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2020-07-18T17:49:31.312597+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HSD17B4 were changed from  to Perrault syndrome 1, MIM# 233400","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2020-07-18T17:49:09.565134+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HSD17B4 were set to ","entity_name":"HSD17B4","entity_type":"gene"},{"created":"2020-07-18T17:48:48.788934+10:00","panel_name":"Disorders of Sex Differentiation","panel_id":99,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HSD17B4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HSD17B4","entity_type":"gene"}]}