{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2018","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2016","results":[{"created":"2019-12-31T14:29:35.982028+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.493","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIABLO were set to ","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:29:15.908217+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.492","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIABLO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:29:01.399142+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.491","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DIABLO as Red List (low evidence)","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:29:01.387544+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.491","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: diablo has been classified as Red List (Low Evidence).","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:28:43.761480+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DIABLO: Rating: RED; Mode of pathogenicity: None; Publications: 21722859, 10929711; Phenotypes: Deafness, autosomal dominant 64, MIM# 614152; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:27:06.770650+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIABLO as ready","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:27:06.757650+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: diablo has been classified as Red List (Low Evidence).","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:27:02.358657+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.116","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIABLO was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:26:18.327794+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIABLO were set to ","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:25:53.806188+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIABLO were changed from  to Deafness, autosomal dominant 64, MIM#\t614152","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:25:17.125930+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DIABLO as Red List (low evidence)","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:25:17.113676+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: diablo has been classified as Red List (Low Evidence).","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:24:27.185513+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIAPH3 as ready","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:24:27.173965+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: diaph3 has been classified as Red List (Low Evidence).","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:24:19.063135+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.490","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIAPH3 were changed from  to Auditory neuropathy, autosomal dominant, 1, MIM#609129","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:24:05.353031+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.489","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DIAPH3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:23:44.881872+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.488","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DIAPH3 were set to ","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:23:29.258818+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.487","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DIAPH3 as Red List (low evidence)","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:23:29.246349+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.487","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: diaph3 has been classified as Red List (Low Evidence).","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:23:11.739045+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DIAPH3: Rating: RED; Mode of pathogenicity: None; Publications: 23441200, 20624953; Phenotypes: Auditory neuropathy, autosomal dominant, 1, MIM#609129; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DIAPH3","entity_type":"gene"},{"created":"2019-12-31T14:20:37.527067+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1452","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DMXL2 as ready","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:20:37.514047+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1452","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:20:31.266665+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1452","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DMXL2 as Green List (high evidence)","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:20:31.254291+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1452","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:20:19.842152+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1451","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DMXL2 was added\ngene: DMXL2 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: DMXL2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DMXL2 were set to 31688942; 30237576\nPhenotypes for gene: DMXL2 were set to Epileptic encephalopathy, early infantile, 81, MIM#\t618663\nReview for gene: DMXL2 was set to GREEN\nAdded comment: Four unrelated families reported. \nSources: Literature","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:50.774959+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DMXL2 as ready","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:50.762774+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:46.832558+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DMXL2 as Green List (high evidence)","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:46.818976+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:06.937764+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DMXL2 as ready","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:18:06.924591+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:17:58.340326+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DMXL2 as Green List (high evidence)","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:17:58.327105+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.486","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:17:40.747796+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.485","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DMXL2 was added\ngene: DMXL2 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: DMXL2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DMXL2 were set to 31688942; 30237576\nPhenotypes for gene: DMXL2 were set to Epileptic encephalopathy, early infantile, 81, MIM#\t618663\nReview for gene: DMXL2 was set to GREEN\nAdded comment: Four unrelated families reported. \nSources: Literature","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:16:20.093791+11:00","panel_name":"Genetic Epilepsy_AustralianGenomics_VCGS","panel_id":202,"panel_version":"0.58","user_name":"Zornitza Stark","item_type":"entity","text":"gene: DMXL2 was added\ngene: DMXL2 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: DMXL2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: DMXL2 were set to 31688942; 30237576\nPhenotypes for gene: DMXL2 were set to Epileptic encephalopathy, early infantile, 81, MIM#\t618663\nReview for gene: DMXL2 was set to GREEN\nAdded comment: Four unrelated families reported. \nSources: Literature","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:11:54.412929+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: DMXL2 as Green List (high evidence)","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:11:54.401140+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dmxl2 has been classified as Green List (High Evidence).","entity_name":"DMXL2","entity_type":"gene"},{"created":"2019-12-31T14:11:46.557369+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ELMOD3 as ready","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:11:46.543815+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: elmod3 has been classified as Amber List (Moderate Evidence).","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:11:00.908581+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.484","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ELMOD3 were changed from  to Deafness, autosomal recessive 88, MIM# 615429; Deafness, autosomal dominant","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:10:40.383848+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.483","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ELMOD3 were set to ","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:10:26.931956+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.482","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ELMOD3 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:10:18.856364+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.481","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ELMOD3 as Amber List (moderate evidence)","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:10:18.843728+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.481","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: elmod3 has been classified as Amber List (Moderate Evidence).","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:10:01.295084+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ELMOD3: Rating: AMBER; Mode of pathogenicity: None; Publications: 24039609, 31628468, 30284680, 29713870; Phenotypes: Deafness, autosomal recessive 88, MIM# 615429, Deafness, autosomal dominant; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"ELMOD3","entity_type":"gene"},{"created":"2019-12-31T14:08:04.462540+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPS8 as ready","entity_name":"EPS8","entity_type":"gene"},{"created":"2019-12-31T14:08:04.450722+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eps8 has been classified as Green List (High Evidence).","entity_name":"EPS8","entity_type":"gene"},{"created":"2019-12-31T14:07:57.717638+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: EPS8 were changed from  to Deafness, autosomal recessive 102, MIM#\t615974","entity_name":"EPS8","entity_type":"gene"},{"created":"2019-12-31T14:07:30.847116+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: EPS8 were set to ","entity_name":"EPS8","entity_type":"gene"},{"created":"2019-12-31T14:06:53.556317+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: EPS8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"EPS8","entity_type":"gene"},{"created":"2019-12-31T14:06:05.090767+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: EPS8L2 as ready","entity_name":"EPS8L2","entity_type":"gene"},{"created":"2019-12-31T14:06:05.079560+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eps8l2 has been classified as Green List (High Evidence).","entity_name":"EPS8L2","entity_type":"gene"},{"created":"2019-12-31T14:05:55.105743+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: EPS8L2 as Green List (high evidence)","entity_name":"EPS8L2","entity_type":"gene"},{"created":"2019-12-31T14:05:55.087079+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.480","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: eps8l2 has been classified as Green List (High Evidence).","entity_name":"EPS8L2","entity_type":"gene"},{"created":"2019-12-31T14:05:38.191735+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.479","user_name":"Zornitza Stark","item_type":"entity","text":"gene: EPS8L2 was added\ngene: EPS8L2 was added to Mendeliome_VCGS. Sources: Expert list\nMode of inheritance for gene: EPS8L2 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: EPS8L2 were set to 26282398; 23918390; 28281779\nPhenotypes for gene: EPS8L2 were set to Deafness autosomal recessive 106, MIM#\t617637\nReview for gene: EPS8L2 was set to GREEN\nAdded comment: Two unrelated families and a mouse model. \nSources: Expert list","entity_name":"EPS8L2","entity_type":"gene"},{"created":"2019-12-31T13:57:09.571027+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRXCR2 as ready","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:57:09.558678+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grxcr2 has been classified as Amber List (Moderate Evidence).","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:57:01.855898+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.478","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GRXCR2 were changed from  to Deafness, autosomal recessive 101, MIM# 615837","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:55:54.778508+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXI1 were set to 29242249; 9843211","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:55:39.380320+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FOXI1 as ready","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:55:39.365938+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: foxi1 has been classified as Green List (High Evidence).","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:55:19.867261+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.477","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GRXCR2 were set to ","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:55:06.619522+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GRXCR2 as Amber List (moderate evidence)","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:55:06.608034+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.476","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grxcr2 has been classified as Amber List (Moderate Evidence).","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:54:48.175258+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.475","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GRXCR2: Rating: AMBER; Mode of pathogenicity: None; Publications: 24619944; Phenotypes: Deafness, autosomal recessive 101, MIM# 615837; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:53:40.153761+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXI1 were set to 29242249; 9843211","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:53:19.894547+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FOXI1 were set to ","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:52:55.998548+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GRXCR2 were set to 24619944","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:52:34.654478+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXI1 were changed from sensorineural deafness and distal renal tubular acidosis to Enlarged vestibular aqueduct, MIM#\t600791","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:52:26.841081+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GRXCR2 as ready","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:52:26.828392+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grxcr2 has been classified as Amber List (Moderate Evidence).","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:51:49.410453+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: FOXI1 were changed from  to sensorineural deafness and distal renal tubular acidosis","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:51:19.978705+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: FOXI1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"FOXI1","entity_type":"gene"},{"created":"2019-12-31T13:49:53.002133+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GRXCR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:49:24.362209+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GRXCR2 were set to ","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:48:50.497347+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GRXCR2 were changed from  to Deafness, autosomal recessive 101, MIM#\t615837","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:48:08.910972+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GRXCR2 as Amber List (moderate evidence)","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:48:08.897977+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: grxcr2 has been classified as Amber List (Moderate Evidence).","entity_name":"GRXCR2","entity_type":"gene"},{"created":"2019-12-31T13:46:58.900429+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.475","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HARS were changed from  to Charcot-Marie-Tooth disease, axonal, type 2W, MIM# 616625","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T13:46:41.219654+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.474","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HARS were set to ","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T13:46:30.471667+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.474","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HARS was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T13:46:00.442310+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.473","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: HARS: Rating: GREEN; Mode of pathogenicity: None; Publications: 26072516; Phenotypes: Charcot-Marie-Tooth disease, axonal, type 2W, MIM# 616625; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"HARS","entity_type":"gene"},{"created":"2019-12-31T13:37:12.870137+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HARS2 as ready","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:37:12.856318+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hars2 has been classified as Green List (High Evidence).","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:37:09.098716+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HARS2 were changed from Perrault syndrome 2, MIM#\t614926 to Perrault syndrome 2, MIM#\t614926","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:36:38.602889+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: HARS2 were changed from  to Perrault syndrome 2, MIM#\t614926","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:36:17.642373+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: HARS2 were set to ","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:35:53.218957+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: HARS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"HARS2","entity_type":"gene"},{"created":"2019-12-31T13:34:12.515373+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KARS as ready","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T13:34:12.503577+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kars has been classified as Green List (High Evidence).","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T13:33:57.657325+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KARS were changed from  to Deafness, autosomal recessive 89, MIM#\t613916","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T13:33:33.450555+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KARS were set to ","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T13:33:09.789373+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KARS was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KARS","entity_type":"gene"},{"created":"2019-12-31T13:30:22.940992+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KCNJ10 as ready","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:30:22.935351+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Note that it is the association with isolated deafness that is disputed. There is ample evidence that bi-allelic variants cause syndromic deafness.","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:30:22.890377+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kcnj10 has been classified as Green List (High Evidence).","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:30:19.417904+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KCNJ10 were changed from  to SESAME syndrome, MIM#\t612780","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:29:53.101008+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KCNJ10 were set to ","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:28:19.605749+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KCNJ10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2019-12-31T13:25:01.573351+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LARS2 as ready","entity_name":"LARS2","entity_type":"gene"}]}