{"count":220725,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1559","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1557","results":[{"created":"2020-10-03T14:40:42.518631+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.583","user_name":"Zornitza Stark","item_type":"entity","text":"gene: CEP250 was added\ngene: CEP250 was added to Deafness_IsolatedAndComplex. Sources: Expert list\nMode of inheritance for gene: CEP250 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: CEP250 were set to 24780881; 29718797; 30459346\nPhenotypes for gene: CEP250 were set to Cone-rod dystrophy and hearing loss 2, MIM# 618358\nReview for gene: CEP250 was set to GREEN\nAdded comment: Cone-rod dystrophy and hearing loss-2 (CRDHL2) is characterized by retinal dystrophy, with photophobia and progressive reduction in visual acuity, associated with sensorineural hearing loss. Three unrelated families reported. \nSources: Expert list","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-10-03T14:39:30.104928+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX1 as ready","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:39:30.085168+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:39:17.545257+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PEX1 as Green List (high evidence)","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:39:17.537028+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.582","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:38:54.660495+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.581","user_name":"Zornitza Stark","item_type":"entity","text":"gene: PEX1 was added\ngene: PEX1 was added to Deafness_IsolatedAndComplex. Sources: Expert list\nMode of inheritance for gene: PEX1 was set to BIALLELIC, autosomal or pseudoautosomal\nPublications for gene: PEX1 were set to 32596134; 31831025; 27872819; 27633571; 27302843\nPhenotypes for gene: PEX1 were set to Heimler syndrome 1, MIM# 234580\nReview for gene: PEX1 was set to GREEN\nAdded comment: Heimler syndrome-1 (HMLR1), which represents the mildest end of the peroxisomal biogenesis disorder spectrum, is a rare autosomal recessive disorder characterised by sensorineural hearing loss, enamel hyoplasia of the secondary dentition, nail abnormalities, and retinitis pigmentosa. More than 5 unrelated families reported. \nSources: Expert list","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:37:45.575891+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PEX1 as ready","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:37:45.564096+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pex1 has been classified as Green List (High Evidence).","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:37:42.721173+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.28","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PEX1 were set to ","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:37:17.825351+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PEX1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32596134, 31831025, 27872819, 27633571, 27302843; Phenotypes: Heimler syndrome 1, MIM# 234580; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PEX1","entity_type":"gene"},{"created":"2020-10-03T14:34:21.739297+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PDZD7 as ready","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:34:21.730305+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdzd7 has been classified as Amber List (Moderate Evidence).","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:34:19.006584+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.27","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PDZD7 were set to ","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:34:07.390768+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: PDZD7 as Amber List (moderate evidence)","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:34:07.379157+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.26","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pdzd7 has been classified as Amber List (Moderate Evidence).","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:33:57.279621+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"changed review comment from: Multiple families reported, supportive functional data, including animal model. DEFINITIVE by ClinGen.; to: Association with deafness: Multiple families reported, supportive functional data, including animal model. DEFINITIVE by ClinGen.\r\n\r\nAssociation with Usher syndrome: only reported in conjunction with other Usher syndrome variants, digenic inheritance model proposed, PMID: 20440071","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:33:05.382315+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: PDZD7: Changed rating: AMBER; Changed publications: 20440071, 19028668, 26416264, 26849169, 27068579, 26445815, 28173822, 24334608; Changed phenotypes: Usher syndrome, type IIC, GPR98/PDZD7 digenic, MIM# 605472, Deafness, autosomal recessive 57, MIM# 618003","entity_name":"PDZD7","entity_type":"gene"},{"created":"2020-10-03T14:30:16.134450+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PCDH15 as ready","entity_name":"PCDH15","entity_type":"gene"},{"created":"2020-10-03T14:30:16.123888+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pcdh15 has been classified as Green List (High Evidence).","entity_name":"PCDH15","entity_type":"gene"},{"created":"2020-10-03T14:30:00.517549+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.25","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PCDH15 were set to ","entity_name":"PCDH15","entity_type":"gene"},{"created":"2020-10-03T14:29:19.667987+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP78 as ready","entity_name":"CEP78","entity_type":"gene"},{"created":"2020-10-03T14:29:19.655819+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep78 has been classified as Green List (High Evidence).","entity_name":"CEP78","entity_type":"gene"},{"created":"2020-10-03T14:29:16.661138+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP78 were set to ","entity_name":"CEP78","entity_type":"gene"},{"created":"2020-10-03T14:29:00.899796+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CEP250 as ready","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-10-03T14:29:00.888002+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cep250 has been classified as Green List (High Evidence).","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-10-03T14:28:57.346592+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CEP250 were set to ","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-10-03T14:27:48.982066+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CEP250: Rating: GREEN; Mode of pathogenicity: None; Publications: 24780881, 29718797, 30459346; Phenotypes: Cone-rod dystrophy and hearing loss 2, MIM# 618358; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CEP250","entity_type":"gene"},{"created":"2020-10-03T14:25:14.763872+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CDH23 as ready","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-10-03T14:25:14.751346+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cdh23 has been classified as Green List (High Evidence).","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-10-03T14:25:10.643021+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CDH23 were set to ","entity_name":"CDH23","entity_type":"gene"},{"created":"2020-10-03T14:24:45.953635+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ADGRV1 as ready","entity_name":"ADGRV1","entity_type":"gene"},{"created":"2020-10-03T14:24:45.945144+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: adgrv1 has been classified as Green List (High Evidence).","entity_name":"ADGRV1","entity_type":"gene"},{"created":"2020-10-03T14:24:43.264355+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ADGRV1 were changed from Usher syndrome,  type 2C to Usher syndrome,  type 2C, MIM# 605472","entity_name":"ADGRV1","entity_type":"gene"},{"created":"2020-10-03T14:24:32.998779+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ADGRV1 were set to ","entity_name":"ADGRV1","entity_type":"gene"},{"created":"2020-10-03T14:24:12.167503+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ABHD12 as ready","entity_name":"ABHD12","entity_type":"gene"},{"created":"2020-10-03T14:24:12.159396+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: abhd12 has been classified as Green List (High Evidence).","entity_name":"ABHD12","entity_type":"gene"},{"created":"2020-10-03T14:24:10.068832+10:00","panel_name":"Usher Syndrome","panel_id":3086,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ABHD12 were set to ","entity_name":"ABHD12","entity_type":"gene"},{"created":"2020-10-03T14:19:06.597994+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.580","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: KCNJ10: Changed rating: GREEN; Changed phenotypes: SESAME syndrome 612780; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"KCNJ10","entity_type":"gene"},{"created":"2020-10-03T14:17:14.315265+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4766","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPRN as ready","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:17:14.305236+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4766","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tprn has been classified as Green List (High Evidence).","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:17:08.570027+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4766","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TPRN were changed from  to Deafness, autosomal recessive 79, MIM# 613307","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:16:51.513264+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4765","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TPRN were set to ","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:13:14.043661+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4764","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TPRN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:12:55.508679+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4763","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TPRN: Rating: GREEN; Mode of pathogenicity: None; Publications: 19603065, 20170898, 20170899, 23340767, 25129962, 20170899, 20170899, 27693694, 24285636; Phenotypes: Deafness, autosomal recessive 79, MIM# 613307; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:12:07.329845+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.580","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TPRN as ready","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:12:07.319600+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.580","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tprn has been classified as Green List (High Evidence).","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:12:04.119224+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.580","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TPRN were changed from  to Deafness, autosomal recessive 79, MIM# 613307","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:11:42.681032+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.579","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TPRN were set to ","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:11:16.028525+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.578","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TPRN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:10:49.482138+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TPRN: Changed phenotypes: Deafness, autosomal recessive 79, MIM# 613307","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T14:10:35.403155+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TPRN: Rating: GREEN; Mode of pathogenicity: None; Publications: 19603065, 20170898, 20170899, 23340767, 25129962, 20170899, 20170899, 27693694, 24285636; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TPRN","entity_type":"gene"},{"created":"2020-10-03T13:05:00.224958+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4763","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMC1 as ready","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:05:00.214928+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4763","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmc1 has been classified as Green List (High Evidence).","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:04:53.169309+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4763","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMC1 were changed from  to Deafness, autosomal dominant 36, MIM# 606705; Deafness, autosomal recessive 7, MIM# 600974","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:04:27.754056+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4762","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMC1 were set to ","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:04:07.911828+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4761","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMC1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:03:49.460977+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4760","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11850618, 17250663, 18616530, 24827932, 11850623, 22105175; Phenotypes: Deafness, autosomal dominant 36, MIM# 606705, Deafness, autosomal recessive 7, MIM# 600974; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:02:38.712720+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMC1 as ready","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:02:38.694616+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmc1 has been classified as Green List (High Evidence).","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:02:36.477962+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.577","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMC1 were changed from  to Deafness, autosomal dominant 36, MIM# 606705; Deafness, autosomal recessive 7, MIM# 600974","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:02:13.474058+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.576","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMC1 were set to ","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:01:45.162892+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.575","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMC1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T13:01:17.972987+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11850618, 17250663, 18616530, 24827932, 11850623, 22105175; Phenotypes: Deafness, autosomal dominant 36, MIM# 606705, Deafness, autosomal recessive 7, MIM# 600974; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"TMC1","entity_type":"gene"},{"created":"2020-10-03T12:56:38.992034+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4760","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMIE as ready","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:56:38.981720+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4760","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmie has been classified as Green List (High Evidence).","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:56:32.847487+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4760","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMIE were changed from  to Deafness, autosomal recessive 6, MIM# 600971","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:56:16.504445+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4759","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMIE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:55:53.901885+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4758","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMIE were set to ","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:55:14.403184+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4757","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMIE: Rating: GREEN; Mode of pathogenicity: None; Publications: 12145746, 19438934, 24416283, 25467981, 25475183, 19934034, 12140191; Phenotypes: Deafness, autosomal recessive 6, MIM# 600971; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:53:43.140408+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TMIE as ready","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:53:43.129278+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tmie has been classified as Green List (High Evidence).","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:53:39.754258+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.574","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TMIE were changed from  to Deafness, autosomal recessive 6, MIM# 600971","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:53:07.191171+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.573","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TMIE were set to ","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:52:39.989144+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.572","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TMIE was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:52:11.977098+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.571","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TMIE: Rating: GREEN; Mode of pathogenicity: None; Publications: 12145746, 19438934, 24416283, 25467981, 25475183, 19934034, 12140191; Phenotypes: Deafness, autosomal recessive 6, MIM# 600971; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TMIE","entity_type":"gene"},{"created":"2020-10-03T12:49:25.643515+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4757","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIOBP as ready","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:49:25.635150+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4757","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: triobp has been classified as Green List (High Evidence).","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:49:19.057207+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4757","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIOBP were changed from  to Deafness, autosomal recessive 28, MIM# 609823","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:49:02.141756+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4756","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIOBP were set to ","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:48:46.726455+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4755","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIOBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:48:28.923601+10:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.4754","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRIOBP: Rating: GREEN; Mode of pathogenicity: None; Publications: 16385458, 16385457, 23226338, 27014650, 24853665, 27344577, 20510926; Phenotypes: Deafness, autosomal recessive 28, MIM# 609823; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:47:32.104129+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.571","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TRIOBP as ready","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:47:32.093061+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.571","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: triobp has been classified as Green List (High Evidence).","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:47:28.930987+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.571","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TRIOBP were changed from  to Deafness, autosomal recessive 28, MIM# 609823","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:47:05.062712+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.570","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TRIOBP were set to ","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:46:36.675689+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.569","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TRIOBP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:46:11.125898+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TRIOBP: Rating: GREEN; Mode of pathogenicity: None; Publications: 16385458, 16385457, 23226338, 27014650, 24853665, 27344577, 20510926; Phenotypes: Deafness, autosomal recessive 28, MIM# 609823; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TRIOBP","entity_type":"gene"},{"created":"2020-10-03T12:43:43.661561+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USH1C as ready","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:43:43.652516+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ush1c has been classified as Green List (High Evidence).","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:43:41.559450+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.568","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USH1C were changed from  to Usher syndrome, type 1C, MIM# 276904; Deafness, autosomal recessive 18A, MIM# 602092","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:43:19.452878+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.567","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: USH1C were set to ","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:42:44.825322+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.566","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: USH1C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:42:14.252608+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: USH1C: Rating: GREEN; Mode of pathogenicity: None; Publications: 10973247, 10973248, 11239869, 21203349, 12107438; Phenotypes: Usher syndrome, type 1C, MIM# 276904, Deafness, autosomal recessive 18A, MIM# 602092; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"USH1C","entity_type":"gene"},{"created":"2020-10-03T12:27:12.138647+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USH1G as ready","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-10-03T12:27:12.129526+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ush1g has been classified as Green List (High Evidence).","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-10-03T12:27:09.716981+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.565","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: USH1G were changed from  to Usher syndrome, type 1G, MIM# 606943","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-10-03T12:26:42.675157+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.564","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: USH1G was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-10-03T12:26:19.268864+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: USH1G: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Usher syndrome, type 1G, MIM# 606943; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"USH1G","entity_type":"gene"},{"created":"2020-10-03T12:24:45.839280+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: USH2A as ready","entity_name":"USH2A","entity_type":"gene"},{"created":"2020-10-03T12:24:45.828091+10:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"0.563","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ush2a has been classified as Green List (High Evidence).","entity_name":"USH2A","entity_type":"gene"}]}