{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1672","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1670","results":[{"created":"2020-08-15T16:39:56.198839+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.115","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MFAP5 were set to ","entity_name":"MFAP5","entity_type":"gene"},{"created":"2020-08-15T16:39:30.980495+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.114","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MFAP5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MFAP5","entity_type":"gene"},{"created":"2020-08-15T16:39:06.139558+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MFAP5 as Amber List (moderate evidence)","entity_name":"MFAP5","entity_type":"gene"},{"created":"2020-08-15T16:39:06.131191+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.113","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mfap5 has been classified as Amber List (Moderate Evidence).","entity_name":"MFAP5","entity_type":"gene"},{"created":"2020-08-15T16:38:39.809686+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MFAP5: Rating: AMBER; Mode of pathogenicity: None; Publications: 25434006, 30763214; Phenotypes: Aortic aneurysm, familial thoracic MIM# 616166; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MFAP5","entity_type":"gene"},{"created":"2020-08-15T16:37:18.792598+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED12 as ready","entity_name":"MED12","entity_type":"gene"},{"created":"2020-08-15T16:37:18.784164+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: med12 has been classified as Green List (High Evidence).","entity_name":"MED12","entity_type":"gene"},{"created":"2020-08-15T16:37:15.069866+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.112","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED12 were changed from  to Lujan-Fryns syndrome, MIM# 309520","entity_name":"MED12","entity_type":"gene"},{"created":"2020-08-15T16:36:48.685212+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.111","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MED12 was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"MED12","entity_type":"gene"},{"created":"2020-08-15T16:36:23.315112+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MED12: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Lujan-Fryns syndrome, MIM# 309520; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"MED12","entity_type":"gene"},{"created":"2020-08-15T16:34:17.864307+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MECOM as ready","entity_name":"MECOM","entity_type":"gene"},{"created":"2020-08-15T16:34:17.852764+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecom has been classified as Green List (High Evidence).","entity_name":"MECOM","entity_type":"gene"},{"created":"2020-08-15T16:34:13.651399+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MECOM as Green List (high evidence)","entity_name":"MECOM","entity_type":"gene"},{"created":"2020-08-15T16:34:13.643180+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.110","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mecom has been classified as Green List (High Evidence).","entity_name":"MECOM","entity_type":"gene"},{"created":"2020-08-15T16:33:51.886700+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.109","user_name":"Zornitza Stark","item_type":"entity","text":"gene: MECOM was added\ngene: MECOM was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: MECOM was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPhenotypes for gene: MECOM were set to Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, MIM#\t616738\nReview for gene: MECOM was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list","entity_name":"MECOM","entity_type":"gene"},{"created":"2020-08-15T14:08:05.896838+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAT2A as ready","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:08:05.886743+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat2a has been classified as Amber List (Moderate Evidence).","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:08:01.478783+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.108","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAT2A were changed from Thoracic aortic aneurysm to Thoracic aortic aneurysm","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:07:36.971097+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3782","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MAT2A as ready","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:07:36.960706+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3782","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat2a has been classified as Amber List (Moderate Evidence).","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:07:20.724636+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3782","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAT2A were changed from  to Thoracic aortic aneurysm","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:07:07.214163+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3781","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAT2A were set to ","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:06:54.746944+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.107","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MAT2A were changed from  to Thoracic aortic aneurysm","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:06:53.342063+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3780","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAT2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:06:24.764616+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3779","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAT2A as Amber List (moderate evidence)","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:06:24.756408+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3779","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat2a has been classified as Amber List (Moderate Evidence).","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:06:09.868250+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3778","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MAT2A: Rating: AMBER; Mode of pathogenicity: None; Publications: 30071989, 25557781; Phenotypes: Thoracic aortic aneurysm; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:05:59.566372+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.106","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MAT2A were set to ","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:05:42.685083+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.105","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MAT2A was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:05:02.202926+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: MAT2A as Amber List (moderate evidence)","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:05:02.193779+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.104","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mat2a has been classified as Amber List (Moderate Evidence).","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:04:40.544991+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: MAT2A: Rating: AMBER; Mode of pathogenicity: None; Publications: 30071989, 25557781; Phenotypes: Thoracic aortic aneurysm; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MAT2A","entity_type":"gene"},{"created":"2020-08-15T14:02:21.731938+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LYST as ready","entity_name":"LYST","entity_type":"gene"},{"created":"2020-08-15T14:02:21.722529+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Green List (High Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2020-08-15T14:02:17.549960+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: LYST as Green List (high evidence)","entity_name":"LYST","entity_type":"gene"},{"created":"2020-08-15T14:02:17.540385+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.103","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lyst has been classified as Green List (High Evidence).","entity_name":"LYST","entity_type":"gene"},{"created":"2020-08-15T14:01:49.884714+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.102","user_name":"Zornitza Stark","item_type":"entity","text":"gene: LYST was added\ngene: LYST was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: LYST was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: LYST were set to Chediak-Higashi syndrome, MIM#\t214500\nReview for gene: LYST was set to GREEN\nAdded comment: Well established gene-disease association, thrombocytopaenia is a feature. \nSources: Expert list","entity_name":"LYST","entity_type":"gene"},{"created":"2020-08-15T13:59:28.390620+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3778","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LOX as ready","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:59:28.380253+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3778","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lox has been classified as Green List (High Evidence).","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:59:19.169415+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3778","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LOX were changed from  to Aortic aneurysm, familial thoracic 10, MIM# 617168","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:59:01.769105+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3777","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LOX were set to ","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:58:38.385449+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3776","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LOX was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:58:24.008179+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LOX as ready","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:58:23.996476+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lox has been classified as Green List (High Evidence).","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:58:21.009130+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.101","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LOX were changed from  to Aortic aneurysm, familial thoracic 10, MIM# 617168","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:57:56.007592+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LOX: Rating: GREEN; Mode of pathogenicity: None; Publications: 30071989, 26838787, 30675029; Phenotypes: Aortic aneurysm, familial thoracic 10, MIM# 617168; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:57:47.903810+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LOX were set to ","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:57:06.869326+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LOX was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:56:39.103344+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: LOX: Added comment: Gene-disease association with aortic aneurysm rated as strong by ClinGen.; Changed publications: 30071989, 26838787, 30675029","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:55:44.024949+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LOX: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Aortic aneurysm, familial thoracic 10, MIM# 617168; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"LOX","entity_type":"gene"},{"created":"2020-08-15T13:51:18.874666+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KDSR as ready","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:51:18.865826+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kdsr has been classified as Green List (High Evidence).","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:51:11.972751+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3775","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KDSR were changed from  to Erythrokeratodermia variabilis et progressiva 4, MIM# 617526; severe thrombocytopaenia","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:50:56.682741+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3774","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KDSR were set to ","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:50:40.155546+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3773","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KDSR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:50:21.646150+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KDSR: Rating: GREEN; Mode of pathogenicity: None; Publications: 28774589, 30467204, 28575652; Phenotypes: Erythrokeratodermia variabilis et progressiva 4, MIM# 617526, severe thrombocytopaenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:49:32.986694+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KDSR as ready","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:49:32.979025+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kdsr has been classified as Green List (High Evidence).","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:49:24.682878+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KDSR were changed from  to Erythrokeratodermia variabilis et progressiva 4, MIM# 617526; severe thrombocytopaenia","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:48:58.843926+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KDSR were set to ","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:48:36.683633+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KDSR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:48:13.418706+10:00","panel_name":"Palmoplantar Keratoderma and Erythrokeratoderma","panel_id":153,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KDSR: Rating: GREEN; Mode of pathogenicity: None; Publications: 28774589, 30467204, 28575652; Phenotypes: Erythrokeratodermia variabilis et progressiva 4, MIM# 617526, severe thrombocytopaenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:46:00.641999+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KDSR as ready","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:46:00.631768+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kdsr has been classified as Green List (High Evidence).","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:45:56.433406+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KDSR as Green List (high evidence)","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:45:56.423227+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kdsr has been classified as Green List (High Evidence).","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:45:23.302337+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.97","user_name":"Zornitza Stark","item_type":"entity","text":"gene: KDSR was added\ngene: KDSR was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: KDSR was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: KDSR were set to 28774589; 30467204\nPhenotypes for gene: KDSR were set to Erythrokeratodermia variabilis et progressiva 4, MIM#\t617526; severe thrombocytopaenia\nReview for gene: KDSR was set to GREEN\nAdded comment: At least 5 families reported where thrombocytopaenia was a significant feature in addition to the eryhtrokeratoderma. \nSources: Expert list","entity_name":"KDSR","entity_type":"gene"},{"created":"2020-08-15T13:20:50.147095+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HOXA11 as ready","entity_name":"HOXA11","entity_type":"gene"},{"created":"2020-08-15T13:20:50.134976+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa11 has been classified as Green List (High Evidence).","entity_name":"HOXA11","entity_type":"gene"},{"created":"2020-08-15T13:20:46.450536+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: HOXA11 as Green List (high evidence)","entity_name":"HOXA11","entity_type":"gene"},{"created":"2020-08-15T13:20:46.440748+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hoxa11 has been classified as Green List (High Evidence).","entity_name":"HOXA11","entity_type":"gene"},{"created":"2020-08-15T13:20:18.678412+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"gene: HOXA11 was added\ngene: HOXA11 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: HOXA11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: HOXA11 were set to 11101832; 16765069\nPhenotypes for gene: HOXA11 were set to Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, MM#\t605432\nReview for gene: HOXA11 was set to GREEN\nAdded comment: Sources: Expert list","entity_name":"HOXA11","entity_type":"gene"},{"created":"2020-08-15T13:16:54.112839+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GNE as ready","entity_name":"GNE","entity_type":"gene"},{"created":"2020-08-15T13:16:54.103461+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gne has been classified as Green List (High Evidence).","entity_name":"GNE","entity_type":"gene"},{"created":"2020-08-15T13:16:50.170232+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GNE as Green List (high evidence)","entity_name":"GNE","entity_type":"gene"},{"created":"2020-08-15T13:16:50.159798+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gne has been classified as Green List (High Evidence).","entity_name":"GNE","entity_type":"gene"},{"created":"2020-08-15T13:16:22.566684+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GNE was added\ngene: GNE was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: GNE was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GNE were set to 30171045; 32505938; 29941673; 25257349\nPhenotypes for gene: GNE were set to Thrombocytopaenia; Myopathy\nReview for gene: GNE was set to GREEN\nAdded comment: Multiple reports of thrombocytopaenia associated with bi-allelic variants in this gene, without or without a muscle phenotype. Note bi-allelic variants classically cause Nonaka myopathy. \nSources: Expert list","entity_name":"GNE","entity_type":"gene"},{"created":"2020-08-15T12:06:51.551705+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GGCX as ready","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:06:51.539866+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ggcx has been classified as Green List (High Evidence).","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:06:45.228856+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3772","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: GGCX were changed from  to Vitamin K-dependent clotting factors, combined deficiency of, 1, MIM# 277450","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:06:29.197742+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3771","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: GGCX were set to ","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:06:12.978590+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3770","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: GGCX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:05:55.396489+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3769","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: GGCX: Rating: GREEN; Mode of pathogenicity: None; Publications: 32785662, 30531603, 26758921; Phenotypes: Vitamin K-dependent clotting factors, combined deficiency of, 1, MIM# 277450; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:04:10.449976+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GGCX as ready","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:04:10.440296+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ggcx has been classified as Green List (High Evidence).","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:04:00.452624+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GGCX as Green List (high evidence)","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:04:00.442598+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ggcx has been classified as Green List (High Evidence).","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T12:03:30.127861+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GGCX was added\ngene: GGCX was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: GGCX was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: GGCX were set to 32785662; 30531603; 26758921\nPhenotypes for gene: GGCX were set to Vitamin K-dependent clotting factors, combined deficiency of, 1, MIM#\t277450\nReview for gene: GGCX was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list","entity_name":"GGCX","entity_type":"gene"},{"created":"2020-08-15T11:55:10.129777+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GBA as ready","entity_name":"GBA","entity_type":"gene"},{"created":"2020-08-15T11:55:10.112915+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gba has been classified as Green List (High Evidence).","entity_name":"GBA","entity_type":"gene"},{"created":"2020-08-15T11:55:06.447397+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GBA as Green List (high evidence)","entity_name":"GBA","entity_type":"gene"},{"created":"2020-08-15T11:55:06.437577+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gba has been classified as Green List (High Evidence).","entity_name":"GBA","entity_type":"gene"},{"created":"2020-08-15T11:54:39.516585+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GBA was added\ngene: GBA was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: GBA was set to BIALLELIC, autosomal or pseudoautosomal\nPhenotypes for gene: GBA were set to Gaucher disease\nReview for gene: GBA was set to GREEN\nAdded comment: Thrombocytopaenia secondary to hypersplenism. \nSources: Expert list","entity_name":"GBA","entity_type":"gene"},{"created":"2020-08-15T11:44:52.129903+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GATA1 as ready","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-08-15T11:44:52.120401+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Green List (High Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-08-15T11:44:49.027803+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: GATA1 as Green List (high evidence)","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-08-15T11:44:49.015357+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: gata1 has been classified as Green List (High Evidence).","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-08-15T11:44:25.943416+10:00","panel_name":"Bleeding Disorders","panel_id":54,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"gene: GATA1 was added\ngene: GATA1 was added to Bleeding Disorders. Sources: Expert list\nMode of inheritance for gene: GATA1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females\nPhenotypes for gene: GATA1 were set to Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, MIM#\t300367\nReview for gene: GATA1 was set to GREEN\nAdded comment: Well established gene-disease association. \nSources: Expert list","entity_name":"GATA1","entity_type":"gene"},{"created":"2020-08-14T20:21:48.442542+10:00","panel_name":"Hydrops fetalis","panel_id":116,"panel_version":"0.163","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Single family reported, two affected individuals. Monoallelic variants in this gene are associated with HHT. \nSources: Literature; to: Single family reported, two affected individuals. Monoallelic variants in this gene are associated with HHT/PAH. \r\nSources: Literature","entity_name":"GDF2","entity_type":"gene"},{"created":"2020-08-14T20:21:29.979280+10:00","panel_name":"Hereditary Haemorrhagic Telangiectasia","panel_id":260,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: GDF2 as ready","entity_name":"GDF2","entity_type":"gene"}]}