{"count":220324,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=904","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=902","results":[{"created":"2022-03-30T09:18:33.767839+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12276","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: ADRB2: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 15724149; Phenotypes: Beta-2-adrenoreceptor agonist, reduced response to, {Asthma, nocturnal, susceptibility to} MIM#600807, {Obesity, susceptibility to} MIM#601665; Mode of inheritance: Unknown","entity_name":"ADRB2","entity_type":"gene"},{"created":"2022-03-30T09:09:34.854973+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4640","user_name":"Elena Savva","item_type":"entity","text":"Phenotypes for gene: WDR11 were changed from Intellectual disability; Microcephaly; Short stature to Neurodevelopmental disorder, MONDO:0700092, WDR11-related","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-03-30T09:09:14.489855+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4640","user_name":"Elena Savva","item_type":"entity","text":"Publications for gene: WDR11 were set to 34413497","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-03-30T09:08:35.227689+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4639","user_name":"Elena Savva","item_type":"entity","text":"Mode of inheritance for gene: WDR11 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-03-30T09:07:57.666398+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4638","user_name":"Elena Savva","item_type":"entity","text":"reviewed gene: WDR11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder,  MONDO:0700092, WDR11-related; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"WDR11","entity_type":"gene"},{"created":"2022-03-29T18:57:12.463749+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12276","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC6A2 as ready","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:57:12.452758+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12276","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a2 has been classified as Red List (Low Evidence).","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:56:26.827572+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12276","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC6A2 were changed from  to Orthostatic intolerance, MIM# 604715","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:56:07.922995+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12275","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SLC6A2 were set to ","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:55:48.985345+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12274","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC6A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:54:24.897228+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12273","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SLC6A2 as Red List (low evidence)","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:54:24.884008+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12273","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc6a2 has been classified as Red List (Low Evidence).","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:54:00.199117+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12272","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC6A2: Rating: RED; Mode of pathogenicity: None; Publications: 10684912; Phenotypes: Orthostatic intolerance, MIM#  604715; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SLC6A2","entity_type":"gene"},{"created":"2022-03-29T18:51:09.177778+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12272","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCAD1 as ready","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:51:09.165818+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12272","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcad1 has been classified as Green List (High Evidence).","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:51:02.630282+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12272","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCAD1 were changed from Huriez syndrome, OMIM #181600; Basan syndrome, MIM# 129200; Adermatoglyphia, MIM# 136000 to Huriez syndrome, OMIM #181600; Basan syndrome, MIM# 129200; Adermatoglyphia, MIM# 136000","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:51:00.295410+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12272","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCAD1 were changed from  to Huriez syndrome, OMIM #181600; Basan syndrome, MIM# 129200; Adermatoglyphia, MIM# 136000","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:50:41.367466+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12271","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMARCAD1 were set to ","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:50:32.583313+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12270","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMARCAD1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:50:23.071780+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12269","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMARCAD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:50:04.235465+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12268","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMARCAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 29409814; Phenotypes: Huriez syndrome, OMIM #181600, Basan syndrome, MIM# 129200, Adermatoglyphia, MIM# 136000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCAD1","entity_type":"gene"},{"created":"2022-03-29T18:47:50.811283+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12268","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMARCB1 as ready","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:47:50.799153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12268","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smarcb1 has been classified as Green List (High Evidence).","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:46:49.704091+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12268","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMARCB1 were changed from  to Coffin-Siris syndrome 3, MIM# 614608","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:46:29.353068+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12267","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: SMARCB1 were set to ","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:46:09.952395+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12266","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMARCB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:45:48.143331+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12265","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMARCB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 34205270, 31530938, 25168959; Phenotypes: Coffin-Siris syndrome 3, MIM# 614608; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"SMARCB1","entity_type":"gene"},{"created":"2022-03-29T18:42:27.939588+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12265","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SMN2 as ready","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:42:27.924225+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12265","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smn2 has been classified as Amber List (Moderate Evidence).","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:42:14.960938+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12265","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SMN2 were changed from  to {Spinal muscular atrophy, type III, modifier of} 253400","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:41:54.444917+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12264","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SMN2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:41:35.723079+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12263","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: SMN2 as Amber List (moderate evidence)","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:41:35.712039+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12263","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: smn2 has been classified as Amber List (Moderate Evidence).","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:41:15.893080+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12262","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SMN2: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: {Spinal muscular atrophy, type III, modifier of} 253400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"SMN2","entity_type":"gene"},{"created":"2022-03-29T18:36:50.173300+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12262","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTOG as ready","entity_name":"OTOG","entity_type":"gene"},{"created":"2022-03-29T18:36:50.159316+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12262","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otog has been classified as Green List (High Evidence).","entity_name":"OTOG","entity_type":"gene"},{"created":"2022-03-29T18:36:42.487228+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12262","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTOG were changed from  to Deafness, autosomal recessive 18B - MIM#614945","entity_name":"OTOG","entity_type":"gene"},{"created":"2022-03-29T18:35:49.171762+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4638","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RAB3GAP2 as ready","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2022-03-29T18:35:49.162183+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4638","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rab3gap2 has been classified as Green List (High Evidence).","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2022-03-29T18:35:44.731448+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4638","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RAB3GAP2 were changed from  to Martsolf syndrome (MIM212720); Warburg micro syndrome 2 (MIM#614225)","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2022-03-29T18:35:09.421864+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4637","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RAB3GAP2 were set to ","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2022-03-29T18:33:32.828097+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.4636","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RAB3GAP2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RAB3GAP2","entity_type":"gene"},{"created":"2022-03-29T17:12:11.454558+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12261","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: EDNRB were changed from  to Waardenburg syndrome type 4A MONDO:0010192; sensorineural hearing loss; pigmentary abnormalities; Hirschsprung disease","entity_name":"EDNRB","entity_type":"gene"},{"created":"2022-03-29T17:06:55.622921+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12260","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: EDNRB were set to ","entity_name":"EDNRB","entity_type":"gene"},{"created":"2022-03-29T16:57:33.510168+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12259","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: EDNRB was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"EDNRB","entity_type":"gene"},{"created":"2022-03-29T16:54:38.723489+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12258","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: EDNRB: Rating: GREEN; Mode of pathogenicity: None; Publications: 28502583, 25852447, 21373256, 16237557, 11773966, 11891690, 8001158, 10528251, 10528251, 19764031, 28236341; Phenotypes: Waardenburg syndrome type 4A (MONDO:0010192); Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal; Current diagnostic: yes","entity_name":"EDNRB","entity_type":"gene"},{"created":"2022-03-29T15:35:04.984922+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.9","user_name":"Bryony Thompson","item_type":"entity","text":"Deleted their review","entity_name":"RGS9BP","entity_type":"gene"},{"created":"2022-03-29T15:34:45.655764+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.9","user_name":"Bryony Thompson","item_type":"entity","text":"Deleted their review","entity_name":"RGS9","entity_type":"gene"},{"created":"2022-03-29T15:30:59.373787+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12258","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OTOG were set to ","entity_name":"OTOG","entity_type":"gene"},{"created":"2022-03-29T15:30:34.295064+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12257","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTOG was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OTOG","entity_type":"gene"},{"created":"2022-03-29T15:30:21.188095+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.9","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: BLOC1S6 were set to 32245340; 22461475","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:29:53.378051+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12256","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTC was changed from X-LINKED: hemizygous mutation in males, biallelic mutations in females to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)","entity_name":"OTC","entity_type":"gene"},{"created":"2022-03-29T15:29:38.871559+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.9","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: BLOC1S6 were set to 22461475; 21665000; 32245340","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:29:30.383162+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.8","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: BLOC1S6 as Green List (high evidence)","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:29:30.364255+11:00","panel_name":"Congenital nystagmus","panel_id":3762,"panel_version":"1.8","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: bloc1s6 has been classified as Green List (High Evidence).","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:29:03.033489+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12255","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OTC as ready","entity_name":"OTC","entity_type":"gene"},{"created":"2022-03-29T15:29:03.022619+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12255","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: otc has been classified as Green List (High Evidence).","entity_name":"OTC","entity_type":"gene"},{"created":"2022-03-29T15:28:44.860045+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.8","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: BLOC1S6 as Green List (high evidence)","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:28:44.830217+11:00","panel_name":"Bleeding and Platelet Disorders","panel_id":54,"panel_version":"1.8","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: bloc1s6 has been classified as Green List (High Evidence).","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:28:01.307147+11:00","panel_name":"Ocular and Oculocutaneous Albinism","panel_id":37,"panel_version":"1.5","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: BLOC1S6 were set to 22461475; 21665000; 32245340","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:26:32.161948+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12255","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OTC were changed from  to Ornithine transcarbamylase deficiency - MIM#311250","entity_name":"OTC","entity_type":"gene"},{"created":"2022-03-29T15:26:08.661065+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12254","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OTC was changed from Unknown to X-LINKED: hemizygous mutation in males, biallelic mutations in females","entity_name":"OTC","entity_type":"gene"},{"created":"2022-03-29T15:24:43.663883+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12253","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSTM1 as ready","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:24:43.651123+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12253","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ostm1 has been classified as Green List (High Evidence).","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:24:40.120518+11:00","panel_name":"Ocular and Oculocutaneous Albinism","panel_id":37,"panel_version":"1.4","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: BLOC1S6 as Green List (high evidence)","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:24:40.107978+11:00","panel_name":"Ocular and Oculocutaneous Albinism","panel_id":37,"panel_version":"1.4","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: bloc1s6 has been classified as Green List (High Evidence).","entity_name":"BLOC1S6","entity_type":"gene"},{"created":"2022-03-29T15:24:36.014216+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSTM1 as ready","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:24:35.999255+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ostm1 has been classified as Green List (High Evidence).","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:15:43.564060+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSTM1 were changed from  to Osteopetrosis, autosomal recessive 5 MIM#259720","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:15:15.635848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12253","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSTM1 were changed from  to Osteopetrosis, autosomal recessive 5 (MIM#259720)","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:15:08.805645+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSTM1 were set to ","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:14:47.708103+11:00","panel_name":"Osteopetrosis","panel_id":150,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSTM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:14:37.146222+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12252","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSTM1 were set to ","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:13:45.176835+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12251","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSTM1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"OSTM1","entity_type":"gene"},{"created":"2022-03-29T15:13:09.006409+11:00","panel_name":"Disorders of immune dysregulation","panel_id":229,"panel_version":"0.129","user_name":"Bryony Thompson","item_type":"panel","text":"Panel types changed to Victorian Clinical Genetics Services; Melbourne Genomics; Rare Disease; Royal Melbourne Hospital","entity_name":null,"entity_type":null},{"created":"2022-03-29T15:12:45.475552+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12250","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSMR as ready","entity_name":"OSMR","entity_type":"gene"},{"created":"2022-03-29T15:12:45.463886+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12250","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: osmr has been classified as Green List (High Evidence).","entity_name":"OSMR","entity_type":"gene"},{"created":"2022-03-29T15:12:36.726063+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12250","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSMR were changed from  to Amyloidosis, primary localized cutaneous, 1 - MIM#105250","entity_name":"OSMR","entity_type":"gene"},{"created":"2022-03-29T15:12:15.282367+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12249","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSMR were set to ","entity_name":"OSMR","entity_type":"gene"},{"created":"2022-03-29T15:11:53.523235+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12248","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSMR was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OSMR","entity_type":"gene"},{"created":"2022-03-29T15:11:20.267869+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12247","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OSBPL2 as ready","entity_name":"OSBPL2","entity_type":"gene"},{"created":"2022-03-29T15:11:20.255579+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12247","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: osbpl2 has been classified as Green List (High Evidence).","entity_name":"OSBPL2","entity_type":"gene"},{"created":"2022-03-29T15:11:12.074239+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12247","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OSBPL2 were changed from  to Deafness, autosomal dominant 67 - MIM#616340","entity_name":"OSBPL2","entity_type":"gene"},{"created":"2022-03-29T15:10:50.640059+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12246","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OSBPL2 were set to ","entity_name":"OSBPL2","entity_type":"gene"},{"created":"2022-03-29T15:10:28.908455+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12245","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OSBPL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OSBPL2","entity_type":"gene"},{"created":"2022-03-29T15:09:52.988961+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12244","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OR2J3 as ready","entity_name":"OR2J3","entity_type":"gene"},{"created":"2022-03-29T15:09:52.967655+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12244","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: or2j3 has been classified as Red List (Low Evidence).","entity_name":"OR2J3","entity_type":"gene"},{"created":"2022-03-29T15:09:43.722766+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12244","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: OR2J3 as Red List (low evidence)","entity_name":"OR2J3","entity_type":"gene"},{"created":"2022-03-29T15:09:43.713401+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12244","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: or2j3 has been classified as Red List (Low Evidence).","entity_name":"OR2J3","entity_type":"gene"},{"created":"2022-03-29T15:09:01.963122+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12243","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OPN1SW as ready","entity_name":"OPN1SW","entity_type":"gene"},{"created":"2022-03-29T15:09:01.949364+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12243","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: opn1sw has been classified as Green List (High Evidence).","entity_name":"OPN1SW","entity_type":"gene"},{"created":"2022-03-29T15:08:51.432860+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12243","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OPN1SW were changed from  to Colourblindness, tritan - MIM#190900","entity_name":"OPN1SW","entity_type":"gene"},{"created":"2022-03-29T15:08:22.673810+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12242","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OPN1SW were set to ","entity_name":"OPN1SW","entity_type":"gene"},{"created":"2022-03-29T15:07:59.534473+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.12241","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OPN1SW was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OPN1SW","entity_type":"gene"},{"created":"2022-03-29T15:07:26.069899+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OPN1MW as ready","entity_name":"OPN1MW","entity_type":"gene"},{"created":"2022-03-29T15:07:26.056753+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: opn1mw has been classified as Amber List (Moderate Evidence).","entity_name":"OPN1MW","entity_type":"gene"},{"created":"2022-03-29T15:07:23.361333+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OPN1MW were changed from Blue cone monochromacy MIM#303700; Colorblindness, deutan MIM#303800 to Blue cone monochromacy MIM#303700; Colourblindness, deutan MIM#303800","entity_name":"OPN1MW","entity_type":"gene"},{"created":"2022-03-29T15:07:16.335419+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OPN1MW were set to 30679166","entity_name":"OPN1MW","entity_type":"gene"},{"created":"2022-03-29T15:07:05.264273+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: OPN1MW as Amber List (moderate evidence)","entity_name":"OPN1MW","entity_type":"gene"},{"created":"2022-03-29T15:07:05.251942+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: opn1mw has been classified as Amber List (Moderate Evidence).","entity_name":"OPN1MW","entity_type":"gene"}]}