{"count":221413,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1758","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1756","results":[{"created":"2020-06-25T20:29:55.271117+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UROS were set to ","entity_name":"UROS","entity_type":"gene"},{"created":"2020-06-25T20:29:30.380512+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UROD as ready","entity_name":"UROD","entity_type":"gene"},{"created":"2020-06-25T20:29:30.371136+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: urod has been classified as Green List (High Evidence).","entity_name":"UROD","entity_type":"gene"},{"created":"2020-06-25T20:29:15.412551+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UROD were set to ","entity_name":"UROD","entity_type":"gene"},{"created":"2020-06-25T20:29:04.634441+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.9","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UROD was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UROD","entity_type":"gene"},{"created":"2020-06-25T20:28:24.156518+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PPOX as ready","entity_name":"PPOX","entity_type":"gene"},{"created":"2020-06-25T20:28:24.146700+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ppox has been classified as Green List (High Evidence).","entity_name":"PPOX","entity_type":"gene"},{"created":"2020-06-25T20:28:21.911170+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.8","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PPOX were changed from Porphyria variegata 176200 to Porphyria variegata, MIM# 176200","entity_name":"PPOX","entity_type":"gene"},{"created":"2020-06-25T20:26:55.902604+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.7","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PPOX were set to ","entity_name":"PPOX","entity_type":"gene"},{"created":"2020-06-25T20:26:17.299521+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: FECH as ready","entity_name":"FECH","entity_type":"gene"},{"created":"2020-06-25T20:26:17.290435+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: fech has been classified as Green List (High Evidence).","entity_name":"FECH","entity_type":"gene"},{"created":"2020-06-25T20:26:12.164418+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.6","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: FECH were set to ","entity_name":"FECH","entity_type":"gene"},{"created":"2020-06-25T20:25:42.307080+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALAS2 as ready","entity_name":"ALAS2","entity_type":"gene"},{"created":"2020-06-25T20:25:42.294566+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alas2 has been classified as Green List (High Evidence).","entity_name":"ALAS2","entity_type":"gene"},{"created":"2020-06-25T20:25:37.653371+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.5","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ALAS2 was changed from X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"ALAS2","entity_type":"gene"},{"created":"2020-06-25T20:25:01.802879+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ALAD as ready","entity_name":"ALAD","entity_type":"gene"},{"created":"2020-06-25T20:25:01.763565+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: alad has been classified as Green List (High Evidence).","entity_name":"ALAD","entity_type":"gene"},{"created":"2020-06-25T20:24:55.478220+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.4","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ALAD were set to ","entity_name":"ALAD","entity_type":"gene"},{"created":"2020-06-25T20:24:31.628183+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: HFE as ready","entity_name":"HFE","entity_type":"gene"},{"created":"2020-06-25T20:24:31.619259+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: hfe has been classified as Red List (Low Evidence).","entity_name":"HFE","entity_type":"gene"},{"created":"2020-06-25T20:24:08.310348+10:00","panel_name":"Porphyria","panel_id":3077,"panel_version":"0.3","user_name":"Zornitza Stark","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Royal Melbourne Hospital; Rare Disease","entity_name":null,"entity_type":null},{"created":"2020-06-25T20:23:05.738904+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3160","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE2A as ready","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:23:05.727546+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3160","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube2a has been classified as Green List (High Evidence).","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:22:56.784769+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3160","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE2A were changed from  to Mental retardation, X-linked syndromic, Nascimento-type (MIM#300860)","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:22:37.288687+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3159","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE2A were set to ","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:22:17.536481+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3158","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBE2A was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:21:56.212651+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.3157","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UBE2A: Rating: GREEN; Mode of pathogenicity: None; Publications: 24053514, 16909393; Phenotypes: Mental retardation, X-linked syndromic, Nascimento-type (MIM#300860); Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:20:46.751860+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2712","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBE2A as ready","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:20:46.738730+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2712","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ube2a has been classified as Green List (High Evidence).","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:20:38.672928+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2712","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBE2A were changed from  to Mental retardation, X-linked syndromic, Nascimento-type (MIM#300860)","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:15:25.855569+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2711","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBE2A were set to ","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:14:11.627914+10:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.2710","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBE2A was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"UBE2A","entity_type":"gene"},{"created":"2020-06-25T20:12:55.059380+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL5A2 as ready","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-06-25T20:12:55.047301+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col5a2 has been classified as Green List (High Evidence).","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-06-25T20:12:49.807767+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.96","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL5A2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-06-25T20:12:26.481214+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: COL5A2 as Green List (high evidence)","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-06-25T20:12:26.468469+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.95","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col5a2 has been classified as Green List (High Evidence).","entity_name":"COL5A2","entity_type":"gene"},{"created":"2020-06-25T19:27:03.672406+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: C1S as ready","entity_name":"C1S","entity_type":"gene"},{"created":"2020-06-25T19:27:03.655863+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: c1s has been classified as Amber List (Moderate Evidence).","entity_name":"C1S","entity_type":"gene"},{"created":"2020-06-25T19:27:01.289231+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.94","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: C1S were changed from  to Ehlers-Danlos syndrome, periodontal type, 1 (MIM# 130080)","entity_name":"C1S","entity_type":"gene"},{"created":"2020-06-25T19:26:31.239212+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.93","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: C1S were set to ","entity_name":"C1S","entity_type":"gene"},{"created":"2020-06-25T19:26:08.375635+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.92","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: C1S was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"C1S","entity_type":"gene"},{"created":"2020-06-25T19:25:17.887895+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR2 as ready","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-06-25T19:25:17.876513+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr2 has been classified as Green List (High Evidence).","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-06-25T19:25:15.049249+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.91","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR2 were changed from  to Loeys-Dietz syndrome 2, MIM#\t610168","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-06-25T19:24:51.208080+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.90","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFBR2 were set to ","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-06-25T19:24:26.379721+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBR2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR2","entity_type":"gene"},{"created":"2020-06-25T19:23:45.735297+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBR1 as ready","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-06-25T19:23:45.721270+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbr1 has been classified as Green List (High Evidence).","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-06-25T19:23:43.224548+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBR1 were changed from  to Loeys-Dietz syndrome 1, MIM#\t609192","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-06-25T19:23:20.013922+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFBR1 were set to ","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-06-25T19:22:51.478906+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBR1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBR1","entity_type":"gene"},{"created":"2020-06-25T19:22:08.931784+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFB3 as ready","entity_name":"TGFB3","entity_type":"gene"},{"created":"2020-06-25T19:22:08.918930+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfb3 has been classified as Green List (High Evidence).","entity_name":"TGFB3","entity_type":"gene"},{"created":"2020-06-25T19:22:05.605759+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFB3 were changed from  to Loeys-Dietz syndrome 5, MI#\t615582","entity_name":"TGFB3","entity_type":"gene"},{"created":"2020-06-25T19:21:18.664159+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFB3 were set to ","entity_name":"TGFB3","entity_type":"gene"},{"created":"2020-06-25T19:20:49.411687+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.83","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFB3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFB3","entity_type":"gene"},{"created":"2020-06-25T19:19:52.021654+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFB2 as ready","entity_name":"TGFB2","entity_type":"gene"},{"created":"2020-06-25T19:19:52.001406+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfb2 has been classified as Green List (High Evidence).","entity_name":"TGFB2","entity_type":"gene"},{"created":"2020-06-25T19:18:01.010965+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.82","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFB2 were changed from  to Loeys-Dietz syndrome 4, MIM#\t614816","entity_name":"TGFB2","entity_type":"gene"},{"created":"2020-06-25T19:17:20.885389+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.81","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFB2 were set to ","entity_name":"TGFB2","entity_type":"gene"},{"created":"2020-06-25T19:16:51.994291+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.80","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFB2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFB2","entity_type":"gene"},{"created":"2020-06-25T19:15:56.336827+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC2A10 as ready","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-06-25T19:15:56.326702+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc2a10 has been classified as Green List (High Evidence).","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-06-25T19:15:53.338969+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.79","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC2A10 were changed from  to Arterial tortuosity syndrome MIM#606145","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-06-25T19:15:24.643121+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.78","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC2A10 were set to ","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-06-25T19:15:00.999872+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC2A10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SLC2A10","entity_type":"gene"},{"created":"2020-06-25T19:13:51.690895+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SKI as ready","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:13:51.685558+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Added comment: Comment when marking as ready: Syndromic connective tissue disorder.","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:13:51.646222+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ski has been classified as Green List (High Evidence).","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:13:39.703955+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SKI were changed from  to Shprintzen-Goldberg syndrome, MIM#164780","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:13:11.125475+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SKI were set to ","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:12:46.255407+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SKI was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SKI","entity_type":"gene"},{"created":"2020-06-25T19:11:55.971950+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRKG1 as ready","entity_name":"PRKG1","entity_type":"gene"},{"created":"2020-06-25T19:11:55.958481+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prkg1 has been classified as Green List (High Evidence).","entity_name":"PRKG1","entity_type":"gene"},{"created":"2020-06-25T19:11:53.418516+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRKG1 were changed from  to Aortic aneurysm, familial thoracic 8, MIM#176894","entity_name":"PRKG1","entity_type":"gene"},{"created":"2020-06-25T19:11:24.568253+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRKG1 were set to ","entity_name":"PRKG1","entity_type":"gene"},{"created":"2020-06-25T19:10:55.990321+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRKG1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PRKG1","entity_type":"gene"},{"created":"2020-06-25T19:10:10.421631+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCGF2 as ready","entity_name":"PCGF2","entity_type":"gene"},{"created":"2020-06-25T19:10:10.408974+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcgf2 has been classified as Green List (High Evidence).","entity_name":"PCGF2","entity_type":"gene"},{"created":"2020-06-25T19:10:07.446322+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PCGF2 were changed from  to Turnpenny-Fry syndrome, MIM#600346","entity_name":"PCGF2","entity_type":"gene"},{"created":"2020-06-25T19:09:38.563041+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCGF2 were set to ","entity_name":"PCGF2","entity_type":"gene"},{"created":"2020-06-25T19:09:10.099512+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PCGF2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PCGF2","entity_type":"gene"},{"created":"2020-06-25T19:08:25.947771+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYLK as ready","entity_name":"MYLK","entity_type":"gene"},{"created":"2020-06-25T19:08:25.938759+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: mylk has been classified as Green List (High Evidence).","entity_name":"MYLK","entity_type":"gene"},{"created":"2020-06-25T19:08:23.345628+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYLK were changed from  to Aortic aneurysm, familial thoracic 7, MIM#600922","entity_name":"MYLK","entity_type":"gene"},{"created":"2020-06-25T19:07:50.314236+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYLK were set to ","entity_name":"MYLK","entity_type":"gene"},{"created":"2020-06-25T19:07:26.813847+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: MYLK was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"MYLK","entity_type":"gene"},{"created":"2020-06-25T19:06:45.180165+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MYH11 as ready","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-06-25T19:06:45.170023+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: myh11 has been classified as Green List (High Evidence).","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-06-25T19:05:21.443927+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MYH11 were changed from  to Aortic aneurysm, familial thoracic 4, MIM#160745","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-06-25T19:04:52.902554+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MYH11 were set to ","entity_name":"MYH11","entity_type":"gene"},{"created":"2020-06-25T19:04:01.219244+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: MED12 as ready","entity_name":"MED12","entity_type":"gene"},{"created":"2020-06-25T19:04:01.207090+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.62","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":"2020-06-25T19:03:57.065804+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: MED12 were changed from  to Lujan-Fryns syndrome, MIM#\t309520; Ohdo syndrome, X-linked, MIM#\t300895; Opitz-Kaveggia syndrome, MIM#\t305450","entity_name":"MED12","entity_type":"gene"},{"created":"2020-06-25T19:02:29.127630+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: MED12 were set to ","entity_name":"MED12","entity_type":"gene"},{"created":"2020-06-25T19:01:58.873939+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.60","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":"2020-06-25T19:00:50.594338+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LOX as ready","entity_name":"LOX","entity_type":"gene"},{"created":"2020-06-25T19:00:50.584764+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.59","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":"2020-06-25T19:00:47.816226+10:00","panel_name":"Aortopathy_Connective Tissue Disorders","panel_id":44,"panel_version":"0.59","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"}]}