{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2017","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=2015","results":[{"created":"2019-12-31T15:58:05.190521+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn9 has been classified as Amber List (Moderate Evidence).","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:57:57.316285+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLDN9 as Amber List (moderate evidence)","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:57:57.304581+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.512","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn9 has been classified as Amber List (Moderate Evidence).","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:57:36.596542+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.511","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLDN9 was added\ngene: CLDN9 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: CLDN9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLDN9 were set to 31175426; 19696885\nPhenotypes for gene: CLDN9 were set to Deafness, autosomal recessive\nReview for gene: CLDN9 was set to AMBER\nAdded comment: Single family with multiple sibs reported; mouse model exhibits deafness. \nSources: Literature","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:57:04.573290+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CLDN9 as ready","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:57:04.561543+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn9 has been classified as Amber List (Moderate Evidence).","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:55:19.046183+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.142","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLDN9 were changed from  to Deafness, autosomal recessive","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:54:50.491467+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLDN9 as Amber List (moderate evidence)","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:54:50.478815+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.141","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cldn9 has been classified as Amber List (Moderate Evidence).","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:54:19.636378+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.140","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CLDN9 was added\ngene: CLDN9 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: CLDN9 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CLDN9 were set to 31175426; 19696885\nReview for gene: CLDN9 was set to AMBER\nAdded comment: Single family with multiple sibs reported; mouse model exhibits deafness. \nSources: Literature","entity_name":"CLDN9","entity_type":"gene"},{"created":"2019-12-31T15:49:50.184329+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOP2B as ready","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:50.171046+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: top2b has been classified as Amber List (Moderate Evidence).","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:40.902354+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TOP2B as ready","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:40.886101+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: top2b has been classified as Amber List (Moderate Evidence).","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:40.590631+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOP2B as Amber List (moderate evidence)","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:40.575202+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.510","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: top2b has been classified as Amber List (Moderate Evidence).","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:36.943994+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: TOP2B as Amber List (moderate evidence)","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:36.928474+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.139","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: top2b has been classified as Amber List (Moderate Evidence).","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:49:08.822784+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.509","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TOP2B was added\ngene: TOP2B was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: TOP2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TOP2B were set to 31198993\nPhenotypes for gene: TOP2B were set to Autosomal dominant deafness\nReview for gene: TOP2B was set to AMBER\nAdded comment: One multigenerational family where variant in this gene segregated; two additional variants identified in a cohort; supportive animal model data. \nSources: Literature","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:46:54.427238+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.138","user_name":"Zornitza Stark","item_type":"entity","text":"gene: TOP2B was added\ngene: TOP2B was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: TOP2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: TOP2B were set to 31198993\nPhenotypes for gene: TOP2B were set to Autosomal dominant deafness\nReview for gene: TOP2B was set to AMBER\nAdded comment: One multigenerational family where variant in this gene segregated; two additional variants identified in a cohort; supportive animal model data. \nSources: Literature","entity_name":"TOP2B","entity_type":"gene"},{"created":"2019-12-31T15:39:39.240447+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BCAP31 as ready","entity_name":"BCAP31","entity_type":"gene"},{"created":"2019-12-31T15:39:39.227378+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bcap31 has been classified as Green List (High Evidence).","entity_name":"BCAP31","entity_type":"gene"},{"created":"2019-12-31T15:39:09.781277+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BCAP31 as Green List (high evidence)","entity_name":"BCAP31","entity_type":"gene"},{"created":"2019-12-31T15:39:09.753836+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.137","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bcap31 has been classified as Green List (High Evidence).","entity_name":"BCAP31","entity_type":"gene"},{"created":"2019-12-31T15:38:33.963225+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.136","user_name":"Zornitza Stark","item_type":"entity","text":"gene: BCAP31 was added\ngene: BCAP31 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: BCAP31 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPublications for gene: BCAP31 were set to 24011989; 31330203; 28332767\nPhenotypes for gene: BCAP31 were set to Deafness, dystonia, and cerebral hypomyelination, MIM#\t300475\nReview for gene: BCAP31 was set to GREEN\nAdded comment: Five unrelated families reported, deafness is part of the phenotype. \nSources: Literature","entity_name":"BCAP31","entity_type":"gene"},{"created":"2019-12-31T15:28:27.474408+11:00","panel_name":"Ichthyosis_VCGS","panel_id":124,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AP1B1 as ready","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:28:27.463605+11:00","panel_name":"Ichthyosis_VCGS","panel_id":124,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:28:22.806712+11:00","panel_name":"Ichthyosis_VCGS","panel_id":124,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP1B1 as Green List (high evidence)","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:28:22.795233+11:00","panel_name":"Ichthyosis_VCGS","panel_id":124,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:26:30.226407+11:00","panel_name":"Ichthyosis_VCGS","panel_id":124,"panel_version":"0.2","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP1B1 was added\ngene: AP1B1 was added to Ichthyosis_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:24:09.193297+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AP1B1 as ready","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:24:09.179394+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:24:00.124229+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1454","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP1B1 as Green List (high evidence)","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:24:00.112955+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1454","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:23:44.163466+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP1B1 as Green List (high evidence)","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:23:44.151581+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.508","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:23:29.335518+11:00","panel_name":"Intellectual disability, syndromic and non-syndromic_GHQ_VCGS","panel_id":250,"panel_version":"0.1453","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP1B1 was added\ngene: AP1B1 was added to Intellectual disability, syndromic and non-syndromic_GHQ_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:21:59.080857+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.507","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP1B1 was added\ngene: AP1B1 was added to Mendeliome_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four unrelated families with bi-allelic LoF variants in this gene. \nSources: Literature","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:18:59.284638+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AP1B1 as ready","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:18:59.272603+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:18:52.916696+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.135","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AP1B1 were changed from Intellectual disability; enteropathy; deafness; peripheral neuropathy; ichthyosis; keratoderma to Intellectual disability; enteropathy; deafness; ichthyosis; keratoderma","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:17:18.396633+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: AP1B1 as Green List (high evidence)","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:17:18.385664+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.134","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ap1b1 has been classified as Green List (High Evidence).","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:16:44.649147+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.133","user_name":"Zornitza Stark","item_type":"entity","text":"gene: AP1B1 was added\ngene: AP1B1 was added to Deafness_MelbourneGenomics_VCGS. Sources: Literature\nMode of inheritance for gene: AP1B1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: AP1B1 were set to 31630788; 31630791\nPhenotypes for gene: AP1B1 were set to Intellectual disability; enteropathy; deafness; peripheral neuropathy; ichthyosis; keratoderma\nReview for gene: AP1B1 was set to GREEN\nAdded comment: Four families reported with bi-allelic LoF variants in this gene. \nSources: Literature","entity_name":"AP1B1","entity_type":"gene"},{"created":"2019-12-31T15:08:32.965667+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADCY1 as ready","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:08:32.953307+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy1 has been classified as Red List (Low Evidence).","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:08:24.993517+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.506","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADCY1 were set to ","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:08:03.551892+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.505","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADCY1 were changed from  to Deafness, autosomal recessive 44, MIM# 610154","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:07:40.637195+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.504","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ADCY1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:06:51.548951+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ADCY1 as Red List (low evidence)","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:06:51.536039+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.503","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adcy1 has been classified as Red List (Low Evidence).","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:06:34.568396+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ADCY1: Rating: RED; Mode of pathogenicity: None; Publications: 24482543; Phenotypes: Deafness, autosomal recessive 44, MIM# 610154; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ADCY1","entity_type":"gene"},{"created":"2019-12-31T15:02:47.578255+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BDP1 as ready","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:02:47.565282+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdp1 has been classified as Red List (Low Evidence).","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:02:38.937058+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.502","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BDP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:02:24.471649+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.501","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BDP1 were changed from  to Deafness, autosomal recessive 112, MIM#618257","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:02:11.420849+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.500","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BDP1 were set to ","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:01:45.630655+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.499","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BDP1 as Red List (low evidence)","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:01:45.616816+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.499","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdp1 has been classified as Red List (Low Evidence).","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T15:01:27.132008+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BDP1: Rating: RED; Mode of pathogenicity: None; Publications: 24312468, 25060281; Phenotypes: Deafness, autosomal recessive 112, MIM#618257; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:58.820505+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BDP1 as ready","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:58.807958+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdp1 has been classified as Red List (Low Evidence).","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:55.807576+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.132","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BDP1 were changed from  to Deafness, autosomal recessive 112, MIM#618257","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:32.089481+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BDP1 were set to ","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:07.296510+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: BDP1 as Red List (low evidence)","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:07.290803+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment on list classification: Single family, nonstop variant.","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:59:07.242651+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.130","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: bdp1 has been classified as Red List (Low Evidence).","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:54:46.980679+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.129","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BDP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BDP1","entity_type":"gene"},{"created":"2019-12-31T14:52:23.593718+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CCDC50 as ready","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:52:23.582513+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc50 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:52:15.204042+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.128","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CCDC50 were set to ","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:51:45.947987+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.127","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CCDC50 were changed from  to Deafness, autosomal dominant 44, MIM#\t607453; Childhood onset deafness, progressive","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:51:06.081950+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.126","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CCDC50 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:50:28.832815+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CCDC50 as Amber List (moderate evidence)","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:50:28.819936+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.125","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ccdc50 has been classified as Amber List (Moderate Evidence).","entity_name":"CCDC50","entity_type":"gene"},{"created":"2019-12-31T14:49:21.231156+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.498","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CLIC5 were changed from  to Deafness, autosomal recessive 103, MIM# 616042","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:48:35.104310+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.497","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLIC5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:47:48.241622+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.496","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CLIC5 were set to ","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:47:29.773345+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.495","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CLIC5 as Amber List (moderate evidence)","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:47:29.761172+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.495","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: clic5 has been classified as Amber List (Moderate Evidence).","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:47:10.255543+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLIC5: Rating: AMBER; Mode of pathogenicity: None; Publications: 24781754, 17021174; Phenotypes: Deafness, autosomal recessive 103, MIM# 616042; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CLIC5","entity_type":"gene"},{"created":"2019-12-31T14:44:52.471151+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP78 as ready","entity_name":"CEP78","entity_type":"gene"},{"created":"2019-12-31T14:44:52.458691+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep78 has been classified as Green List (High Evidence).","entity_name":"CEP78","entity_type":"gene"},{"created":"2019-12-31T14:44:45.383235+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.124","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CEP78 were changed from Cone-rod dystrophy and hearing loss to Cone-rod dystrophy and hearing loss, MIM#617236","entity_name":"CEP78","entity_type":"gene"},{"created":"2019-12-31T14:44:14.924790+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CEP78 as Green List (high evidence)","entity_name":"CEP78","entity_type":"gene"},{"created":"2019-12-31T14:44:14.912964+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.123","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep78 has been classified as Green List (High Evidence).","entity_name":"CEP78","entity_type":"gene"},{"created":"2019-12-31T14:40:10.626155+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CRYM as ready","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:40:10.613707+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crym has been classified as Amber List (Moderate Evidence).","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:40:06.660241+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.122","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYM was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:38:55.505546+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.121","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYM were changed from Deafness, autosomal dominant 40, MIM#\t616357 to Deafness, autosomal dominant 40, MIM#\t616357","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:32:52.197915+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYM was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:32:30.983751+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.120","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CRYM was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:32:07.326898+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CRYM were changed from  to Deafness, autosomal dominant 40, MIM#\t616357","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:31:43.123036+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.119","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYM were set to 12471561; 16740909; 18448257; 24676347; 26915689","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:31:30.529388+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DIABLO as ready","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:31:30.516499+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.494","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":"2019-12-31T14:31:19.548122+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.118","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CRYM were set to ","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:31:16.242187+11:00","panel_name":"Mendeliome_VCGS","panel_id":137,"panel_version":"0.494","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DIABLO were changed from  to Deafness, autosomal dominant 64, MIM# 614152","entity_name":"DIABLO","entity_type":"gene"},{"created":"2019-12-31T14:30:42.536572+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CRYM as Amber List (moderate evidence)","entity_name":"CRYM","entity_type":"gene"},{"created":"2019-12-31T14:30:42.523382+11:00","panel_name":"Deafness_MelbourneGenomics_VCGS","panel_id":209,"panel_version":"0.117","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: crym has been classified as Amber List (Moderate Evidence).","entity_name":"CRYM","entity_type":"gene"}]}