{"count":220212,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=884","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=882","results":[{"created":"2022-04-14T16:28:23.863150+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.259","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RIT1 were set to ","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-04-14T16:27:41.492311+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.258","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RIT1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-04-14T16:27:06.968121+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: RIT1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-04-14T16:26:35.669193+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SHOC2 as ready","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:26:35.659726+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: shoc2 has been classified as Green List (High Evidence).","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:26:32.647951+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.257","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SHOC2 were changed from  to Noonan syndrome-like with loose anagen hair 1, MIM: #607721","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:25:56.047379+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.256","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SHOC2 were set to ","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:25:25.060609+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.255","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SHOC2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:24:53.406641+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.254","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SHOC2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-14T16:22:38.923203+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12910","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCD as ready","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:22:38.901904+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12910","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcd has been classified as Green List (High Evidence).","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:22:29.696280+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12910","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCD were changed from  to Muscular dystrophy, limb-girdle, autosomal recessive 6, MIM# 601287; autosomal recessive limb-girdle muscular dystrophy MONDO:0015152","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:22:08.122471+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12909","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCD were set to ","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:21:46.465092+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12908","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SGCD was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:21:18.700756+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12907","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Association with LGMD is DEFINITIVE by ClinGen.; to: Association with LGMD is DEFINITIVE by ClinGen. More than 10 unrelated families reported.","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:21:02.153917+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12907","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SGCD: Rating: GREEN; Mode of pathogenicity: None; Publications: 8841194, 19259135, 20623375, 10838250, 10735275, 9832045, 30733730; Phenotypes: Muscular dystrophy, limb-girdle, autosomal recessive 6, MIM# 601287, autosomal recessive limb-girdle muscular dystrophy MONDO:0015152; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SGCD","entity_type":"gene"},{"created":"2022-04-14T16:18:09.611028+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12907","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCB as ready","entity_name":"SGCB","entity_type":"gene"},{"created":"2022-04-14T16:18:09.601009+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12907","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgcb has been classified as Green List (High Evidence).","entity_name":"SGCB","entity_type":"gene"},{"created":"2022-04-14T16:17:59.142700+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12907","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCB were changed from  to Muscular dystrophy, limb-girdle, autosomal recessive 4 MIM#604286; autosomal recessive limb-girdle muscular dystrophy, MONDO:0015152","entity_name":"SGCB","entity_type":"gene"},{"created":"2022-04-14T16:17:26.805041+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12906","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCB were set to ","entity_name":"SGCB","entity_type":"gene"},{"created":"2022-04-14T16:17:04.340147+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12905","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SGCB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SGCB","entity_type":"gene"},{"created":"2022-04-14T16:16:26.923136+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCA as ready","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:16:26.911164+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgca has been classified as Green List (High Evidence).","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:16:17.643091+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCA were changed from Limb-girdle muscular dystrophy; Muscular dystrophy, limb-girdle, type 2D, 608099 to Limb-girdle muscular dystrophy; Muscular dystrophy, limb-girdle, type 2D, 608099; autosomal recessive limb-girdle muscular dystrophy, MONDO:0015152","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:15:58.946779+10:00","panel_name":"Limb Girdle Muscular Dystrophy","panel_id":3071,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCA were set to ","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:15:27.070239+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12904","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SGCA as ready","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:15:27.051907+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12904","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sgca has been classified as Green List (High Evidence).","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:15:17.484878+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12904","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SGCA were changed from  to Muscular dystrophy, limb-girdle, autosomal recessive 3 MIM#608099; autosomal recessive limb-girdle muscular dystrophy, MONDO:0015152","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:14:53.396529+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12903","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SGCA were set to ","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:14:31.903536+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12902","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SGCA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SGCA","entity_type":"gene"},{"created":"2022-04-14T16:13:46.253748+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12901","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SFXN4 as ready","entity_name":"SFXN4","entity_type":"gene"},{"created":"2022-04-14T16:13:46.240656+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12901","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sfxn4 has been classified as Green List (High Evidence).","entity_name":"SFXN4","entity_type":"gene"},{"created":"2022-04-14T16:13:26.189937+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12901","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SFXN4 were changed from  to Combined oxidative phosphorylation deficiency 18, MIM#615578","entity_name":"SFXN4","entity_type":"gene"},{"created":"2022-04-14T16:13:05.352400+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12900","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SFXN4 were set to ","entity_name":"SFXN4","entity_type":"gene"},{"created":"2022-04-14T16:12:27.766307+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12899","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SFXN4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SFXN4","entity_type":"gene"},{"created":"2022-04-14T16:11:35.081489+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12898","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SFRP4 as ready","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:11:35.070192+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12898","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sfrp4 has been classified as Green List (High Evidence).","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:11:26.016522+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12898","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SFRP4 were changed from  to Pyle disease, MIM#265900","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:11:04.016285+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12897","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SFRP4 were set to ","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:10:41.934735+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12896","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SFRP4 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:10:18.188997+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12895","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SFRP4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyle disease, MIM#265900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:09:38.215820+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SFRP4 as ready","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:09:38.200438+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: sfrp4 has been classified as Green List (High Evidence).","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:09:34.498270+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SFRP4 were changed from PYL; Pyle disease 265900; Metaphyseal dysplasia to Pyle disease, MIM#265900","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:09:09.232840+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.162","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SFRP4 were set to 28100910; 27355534; 26273529; 27117872; 20174869; 24096177; 22965941; 22387305","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:08:27.924043+10:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.161","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SFRP4: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Pyle disease, MIM# 265900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SFRP4","entity_type":"gene"},{"created":"2022-04-14T16:07:01.577478+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12895","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RASGRP1 as ready","entity_name":"RASGRP1","entity_type":"gene"},{"created":"2022-04-14T16:07:01.564294+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12895","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rasgrp1 has been classified as Green List (High Evidence).","entity_name":"RASGRP1","entity_type":"gene"},{"created":"2022-04-14T16:06:41.590390+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12895","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RASGRP1 were changed from  to Immunodeficiency 64 (MIM#618534)","entity_name":"RASGRP1","entity_type":"gene"},{"created":"2022-04-14T16:06:13.955334+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12894","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RASGRP1 were set to ","entity_name":"RASGRP1","entity_type":"gene"},{"created":"2022-04-14T16:05:50.146616+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12893","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RASGRP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RASGRP1","entity_type":"gene"},{"created":"2022-04-14T16:03:00.995336+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12892","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDCD1 as ready","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T16:03:00.977397+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12892","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdcd1 has been classified as Red List (Low Evidence).","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T16:02:51.113928+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12892","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDCD1 were changed from PDCD1 deficiency to PDCD1 deficiency; Inborn errors of immunity, MONDO:0003778","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T16:00:09.390383+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12891","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PDCD1 were changed from  to PDCD1 deficiency","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T15:59:45.554752+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12890","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDCD1 were set to ","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T15:57:23.507982+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12889","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PDCD1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T15:57:02.517819+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12888","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDCD1 as Red List (low evidence)","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T15:57:02.508104+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12888","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdcd1 has been classified as Red List (Low Evidence).","entity_name":"PDCD1","entity_type":"gene"},{"created":"2022-04-14T15:55:57.550014+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12887","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCK2 as ready","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:55:57.533267+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12887","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pck2 has been classified as Red List (Low Evidence).","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:55:48.339246+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12887","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCK2 were changed from  to PEPCK deficiency, mitochondrial - MIM#261650","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:55:25.559238+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12886","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCK2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:55:04.170082+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12885","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PCK2 as Red List (low evidence)","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:55:04.157495+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12885","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pck2 has been classified as Red List (Low Evidence).","entity_name":"PCK2","entity_type":"gene"},{"created":"2022-04-14T15:53:50.333401+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CD79A as ready","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:53:50.320404+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cd79a has been classified as Green List (High Evidence).","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:53:38.936232+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD79A were changed from  to Agammaglobulinaemia 3, MIM#613501","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:53:08.637028+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CD79A were set to ","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:52:38.606771+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CD79A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:52:04.641228+10:00","panel_name":"Predominantly Antibody Deficiency","panel_id":222,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CD79A: Rating: GREEN; Mode of pathogenicity: None; Publications: 29335801, 31696364, 24481606, 10525050, 11920841; Phenotypes: Agammaglobulinaemia 3, MIM#613501; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:51:22.746189+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12884","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CD79A were changed from Agammaglobulinemia 3 MIM#613501 to Agammaglobulinaemia 3 MIM#613501","entity_name":"CD79A","entity_type":"gene"},{"created":"2022-04-14T15:50:41.534141+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12883","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCCB as ready","entity_name":"PCCB","entity_type":"gene"},{"created":"2022-04-14T15:50:41.524388+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12883","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pccb has been classified as Green List (High Evidence).","entity_name":"PCCB","entity_type":"gene"},{"created":"2022-04-14T15:50:31.506961+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12883","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCCB were changed from  to Propionicacidaemia - MIM#606054","entity_name":"PCCB","entity_type":"gene"},{"created":"2022-04-14T15:49:57.832660+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12882","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCCB were set to ","entity_name":"PCCB","entity_type":"gene"},{"created":"2022-04-14T15:49:33.901525+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12881","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCCB was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PCCB","entity_type":"gene"},{"created":"2022-04-14T15:48:40.489182+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12880","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCCA as ready","entity_name":"PCCA","entity_type":"gene"},{"created":"2022-04-14T15:48:40.479643+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12880","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcca has been classified as Green List (High Evidence).","entity_name":"PCCA","entity_type":"gene"},{"created":"2022-04-14T15:48:15.456480+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12880","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCCA were changed from  to Propionicacidaemia - MIM#606054","entity_name":"PCCA","entity_type":"gene"},{"created":"2022-04-14T15:47:41.601735+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12879","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCCA were set to ","entity_name":"PCCA","entity_type":"gene"},{"created":"2022-04-14T15:47:19.941038+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12878","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCCA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PCCA","entity_type":"gene"},{"created":"2022-04-14T14:59:43.418544+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12877","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: FXR1 were changed from Congenital multi-minicore myopathy; multiminicore myopathy MONDO:0018948 to Congenital multi-minicore myopathy; myopathy, congenital proximal, with minicore lesions MONDO:0032937","entity_name":"FXR1","entity_type":"gene"},{"created":"2022-04-14T14:57:50.685724+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12876","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: FXR1 were changed from Congenital multi-minicore myopathy to Congenital multi-minicore myopathy; multiminicore myopathy MONDO:0018948","entity_name":"FXR1","entity_type":"gene"},{"created":"2022-04-14T14:51:53.629328+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12875","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: FZD5 were changed from Coloboma to Coloboma MONDO:0001476","entity_name":"FZD5","entity_type":"gene"},{"created":"2022-04-14T11:37:50.497202+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.254","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: RAF1: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 17603483, 17603482, 31145547, 31030682, 29271604, 24777450; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"RAF1","entity_type":"gene"},{"created":"2022-04-14T11:31:02.076796+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.254","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: RIT1: Rating: ; Mode of pathogenicity: None; Publications: 25124994, 24939608, 27101134, 23791108, 33082562; Phenotypes: Noonan syndrome-8, MIM:#615355; Mode of inheritance: None","entity_name":"RIT1","entity_type":"gene"},{"created":"2022-04-14T11:24:38.365967+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.254","user_name":"Abhijit Kulkarni","item_type":"entity","text":"reviewed gene: SHOC2: Rating: ; Mode of pathogenicity: None; Publications: 24458587, 33082562, 33027564; Phenotypes: Noonan syndrome-like with loose anagen hair 1, MIM: #607721; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SHOC2","entity_type":"gene"},{"created":"2022-04-13T17:44:53.868672+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12874","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PC as ready","entity_name":"PC","entity_type":"gene"},{"created":"2022-04-13T17:44:53.857276+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12874","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pc has been classified as Green List (High Evidence).","entity_name":"PC","entity_type":"gene"},{"created":"2022-04-13T17:44:38.540103+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12874","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PC were changed from  to Pyruvate carboxylase deficiency - MIM#266150","entity_name":"PC","entity_type":"gene"},{"created":"2022-04-13T17:44:11.305997+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12873","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PC were set to ","entity_name":"PC","entity_type":"gene"},{"created":"2022-04-13T17:41:47.402256+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12872","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PC was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PC","entity_type":"gene"},{"created":"2022-04-13T17:40:56.796587+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12871","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAX9 as ready","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:40:56.783869+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12871","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pax9 has been classified as Green List (High Evidence).","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:40:47.997531+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12871","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PAX9 were changed from  to Tooth agenesis, selective, 3 - MIM#604625","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:40:25.151692+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12870","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PAX9 were set to ","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:39:49.483533+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12869","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PAX9 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:39:08.273011+10:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PAX9 as ready","entity_name":"PAX9","entity_type":"gene"},{"created":"2022-04-13T17:39:08.263485+10:00","panel_name":"Oligodontia","panel_id":148,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pax9 has been classified as Green List (High Evidence).","entity_name":"PAX9","entity_type":"gene"}]}