{"count":221304,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=285","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=283","results":[{"created":"2025-03-18T11:30:57.022552+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1587","user_name":"Lilian Downie","item_type":"entity","text":"Marked gene: GUCY2C as ready","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2025-03-18T11:30:57.016819+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1587","user_name":"Lilian Downie","item_type":"entity","text":"Added comment: Comment when marking as ready: Suggest demoting to orange or red, phenotype is not severe - requires early surgical management and then results in normal growth and development","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2025-03-18T11:30:56.977387+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1587","user_name":"Lilian Downie","item_type":"entity","text":"Gene: gucy2c has been classified as Green List (High Evidence).","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2025-03-18T11:30:27.646256+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1587","user_name":"Lilian Downie","item_type":"entity","text":"Publications for gene: GUCY2C were set to ","entity_name":"GUCY2C","entity_type":"gene"},{"created":"2025-03-16T16:18:11.223542+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.432","user_name":"Bryony Thompson","item_type":"entity","text":"Classified gene: DZIP1 as Amber List (moderate evidence)","entity_name":"DZIP1","entity_type":"gene"},{"created":"2025-03-16T16:18:11.216172+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.432","user_name":"Bryony Thompson","item_type":"entity","text":"Gene: dzip1 has been classified as Amber List (Moderate Evidence).","entity_name":"DZIP1","entity_type":"gene"},{"created":"2025-03-16T16:17:00.866922+11:00","panel_name":"Congenital Heart Defect","panel_id":76,"panel_version":"0.431","user_name":"Bryony Thompson","item_type":"entity","text":"gene: DZIP1 was added\ngene: DZIP1 was added to Congenital Heart Defect. Sources: Literature\nMode of inheritance for gene: DZIP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted\nPublications for gene: DZIP1 were set to 33811421; 31118289\nPhenotypes for gene: DZIP1 were set to mitral valve prolapse MONDO:0004910\nReview for gene: DZIP1 was set to AMBER\nAdded comment: Two unrelated families segregating 2 different missense variants (S24R - 53 hets and C585W - 12,414 alleles & 74 homs in gnomAD v4.1) with mitral valve prolapse. 2 rare missense (Pro47Leu - 10 hets & Arg267Ile - 118 hets in gnomAD v) identified in 2 unrelated sporadic MVP cases. Supporting mouse model of S24R impaired ciliogenesis during development, which progressed to adult myxomatous valve disease and functional MVP. \nSources: Literature","entity_name":"DZIP1","entity_type":"gene"},{"created":"2025-03-16T16:15:41.930555+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2382","user_name":"Bryony Thompson","item_type":"entity","text":"reviewed gene: DZIP1: Rating: AMBER; Mode of pathogenicity: None; Publications: 33811421, 31118289; Phenotypes: mitral valve prolapse MONDO:0004910; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DZIP1","entity_type":"gene"},{"created":"2025-03-15T20:02:34.764848+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2382","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: DYNC1H1 were set to 25512093; 28196890","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2025-03-15T20:02:05.694619+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2381","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: DYNC1H1 were changed from Charcot-Marie-Tooth disease, axonal, type 20; Mental retardation, autosomal dominant 13; Spinal muscular atrophy, lower extremity-predominant 1 to dyneinopathy MONDO:1040031","entity_name":"DYNC1H1","entity_type":"gene"},{"created":"2025-03-15T18:01:51.919106+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2380","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: DUOXA2 were set to ","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2025-03-15T18:00:41.618542+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2379","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: DUOXA2 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"DUOXA2","entity_type":"gene"},{"created":"2025-03-15T17:50:33.230386+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2378","user_name":"Bryony Thompson","item_type":"entity","text":"Phenotypes for gene: DUOXA1 were changed from congenital hypothyroidism, No OMIM # to congenital hypothyroidism MONDO:0018612","entity_name":"DUOXA1","entity_type":"gene"},{"created":"2025-03-15T17:48:34.260907+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2377","user_name":"Bryony Thompson","item_type":"entity","text":"Publications for gene: DUOXA1 were set to 29650690","entity_name":"DUOXA1","entity_type":"gene"},{"created":"2025-03-15T17:48:08.590858+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2376","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: DUOXA1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"DUOXA1","entity_type":"gene"},{"created":"2025-03-15T17:17:08.819840+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2375","user_name":"Bryony Thompson","item_type":"entity","text":"Added comment: Comment on mode of inheritance: Biallelic evidence for IBD is strong, but the evidence for the monoallelic association is limited. Semidominant inheritance for thyroid dyshormonogenesis.","entity_name":"DUOX2","entity_type":"gene"},{"created":"2025-03-15T17:17:08.801924+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2375","user_name":"Bryony Thompson","item_type":"entity","text":"Mode of inheritance for gene: DUOX2 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"DUOX2","entity_type":"gene"},{"created":"2025-03-14T16:19:35.820091+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: LINC01578.","entity_name":"LINC01578","entity_type":"gene"},{"created":"2025-03-14T16:19:20.325742+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: LINC01578.","entity_name":"LINC01578","entity_type":"gene"},{"created":"2025-03-14T16:18:51.588608+11:00","panel_name":"Susceptibility to Viral Infections","panel_id":237,"panel_version":"0.131","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORA31.","entity_name":"SNORA31","entity_type":"gene"},{"created":"2025-03-14T16:18:40.177796+11:00","panel_name":"Defects of intrinsic and innate immunity","panel_id":231,"panel_version":"1.20","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SNORA31 as ready","entity_name":"SNORA31","entity_type":"gene"},{"created":"2025-03-14T16:18:40.171129+11:00","panel_name":"Defects of intrinsic and innate immunity","panel_id":231,"panel_version":"1.20","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: snora31 has been classified as Green List (High Evidence).","entity_name":"SNORA31","entity_type":"gene"},{"created":"2025-03-14T16:18:33.373047+11:00","panel_name":"Defects of intrinsic and innate immunity","panel_id":231,"panel_version":"1.20","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORA31.","entity_name":"SNORA31","entity_type":"gene"},{"created":"2025-03-14T16:18:19.311383+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORA31.","entity_name":"SNORA31","entity_type":"gene"},{"created":"2025-03-14T16:17:34.851050+11:00","panel_name":"Deafness_IsolatedAndComplex","panel_id":209,"panel_version":"1.213","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR96.","entity_name":"MIR96","entity_type":"gene"},{"created":"2025-03-14T16:17:18.266324+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR96.","entity_name":"MIR96","entity_type":"gene"},{"created":"2025-03-14T16:16:57.799580+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR936.","entity_name":"MIR936","entity_type":"gene"},{"created":"2025-03-14T16:16:35.468767+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR5004.","entity_name":"MIR5004","entity_type":"gene"},{"created":"2025-03-14T16:16:14.823700+11:00","panel_name":"Cone-rod Dystrophy","panel_id":3147,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR204.","entity_name":"MIR204","entity_type":"gene"},{"created":"2025-03-14T16:16:04.574567+11:00","panel_name":"Optic Atrophy","panel_id":149,"panel_version":"1.45","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR204.","entity_name":"MIR204","entity_type":"gene"},{"created":"2025-03-14T16:15:48.692214+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR204.","entity_name":"MIR204","entity_type":"gene"},{"created":"2025-03-14T16:15:24.893098+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR184.","entity_name":"MIR184","entity_type":"gene"},{"created":"2025-03-14T16:15:11.896075+11:00","panel_name":"Cataract","panel_id":66,"panel_version":"0.373","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR184.","entity_name":"MIR184","entity_type":"gene"},{"created":"2025-03-14T16:14:48.047055+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR183.","entity_name":"MIR183","entity_type":"gene"},{"created":"2025-03-14T16:14:24.523593+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR182.","entity_name":"MIR182","entity_type":"gene"},{"created":"2025-03-14T16:13:25.554716+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR17HG.","entity_name":"MIR17HG","entity_type":"gene"},{"created":"2025-03-14T16:13:12.675208+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR17HG.","entity_name":"MIR17HG","entity_type":"gene"},{"created":"2025-03-14T16:12:59.175704+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR17HG.","entity_name":"MIR17HG","entity_type":"gene"},{"created":"2025-03-14T16:12:43.982232+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR17HG.","entity_name":"MIR17HG","entity_type":"gene"},{"created":"2025-03-14T16:12:23.917672+11:00","panel_name":"Gastrointestinal neuromuscular disease","panel_id":3087,"panel_version":"1.24","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR145.","entity_name":"MIR145","entity_type":"gene"},{"created":"2025-03-14T16:12:09.561644+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR145.","entity_name":"MIR145","entity_type":"gene"},{"created":"2025-03-14T16:11:48.070132+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR140.","entity_name":"MIR140","entity_type":"gene"},{"created":"2025-03-14T16:11:31.380481+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: MIR140.","entity_name":"MIR140","entity_type":"gene"},{"created":"2025-03-14T16:10:07.455076+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:09:49.816428+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1586","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:09:30.438170+11:00","panel_name":"BabyScreen+ newborn screening","panel_id":3931,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:09:07.400510+11:00","panel_name":"Hair disorders","panel_id":3269,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:08:24.810302+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RSPO4 as ready","entity_name":"RSPO4","entity_type":"gene"},{"created":"2025-03-14T16:08:24.800719+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rspo4 has been classified as Green List (High Evidence).","entity_name":"RSPO4","entity_type":"gene"},{"created":"2025-03-14T16:08:20.888510+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: RSPO4 as Green List (high evidence)","entity_name":"RSPO4","entity_type":"gene"},{"created":"2025-03-14T16:08:20.879504+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.89","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rspo4 has been classified as Green List (High Evidence).","entity_name":"RSPO4","entity_type":"gene"},{"created":"2025-03-14T16:07:46.015199+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:46.009025+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:43.493678+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.88","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMRP were changed from Cartilage-hair hypoplasia, Metaphyseal dysplasia without hypotrichosis, Anauxetic dysplasia to Cartilage hair hypoplasia (CHH) MIM#250250; Anauxetic dysplasia 1, MIM# 607095; Metaphyseal dysplasia without hypotrichosis, MIM# 250460","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:30.478490+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RMRP were set to ","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:21.202128+11:00","panel_name":"Ectodermal Dysplasia","panel_id":3089,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:03.653361+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:03.642895+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:07:00.087630+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.305","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: RMRP were set to ","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:06:36.776810+11:00","panel_name":"Skeletal dysplasia","panel_id":258,"panel_version":"0.304","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:06:22.727847+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:06:09.219096+11:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:57.221665+11:00","panel_name":"Mitochondrial disease","panel_id":203,"panel_version":"0.970","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:30.710285+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:18.341993+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.114","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:07.310645+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: RMRP as ready","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:07.300431+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: rmrp has been classified as Green List (High Evidence).","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:05:04.277124+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.230","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: RMRP were changed from  to Anauxetic dysplasia 1, MIM#607095","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:04:38.466873+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.229","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: RMRP was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:04:18.800785+11:00","panel_name":"Skeletal Dysplasia_Fetal","panel_id":28,"panel_version":"0.228","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RMRP.","entity_name":"RMRP","entity_type":"gene"},{"created":"2025-03-14T16:03:50.316101+11:00","panel_name":"BabyScreen+ newborn screening","panel_id":3931,"panel_version":"1.116","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:29.862171+11:00","panel_name":"IBMDx study","panel_id":3829,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TERC as ready","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:29.855171+11:00","panel_name":"IBMDx study","panel_id":3829,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: terc has been classified as Green List (High Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:25.950678+11:00","panel_name":"IBMDx study","panel_id":3829,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERC were changed from Dyskeratosis congenita, autosomal dominant 1, MIM# 127550 to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:19.488640+11:00","panel_name":"IBMDx study","panel_id":3829,"panel_version":"0.34","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TERC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:13.150275+11:00","panel_name":"IBMDx study","panel_id":3829,"panel_version":"0.33","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:03:00.244439+11:00","panel_name":"Combined Immunodeficiency","panel_id":223,"panel_version":"1.115","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:02:43.524595+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TERC as ready","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:02:43.517123+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: terc has been classified as Green List (High Evidence).","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:02:41.050607+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERC were changed from  to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:02:19.701405+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TERC were set to ","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:01:58.558372+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TERC was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:01:36.607320+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:01:28.376848+11:00","panel_name":"Pulmonary Fibrosis_Interstitial Lung Disease","panel_id":162,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TERC: Changed phenotypes: Dyskeratosis congenita, autosomal dominant 1, MIM# 127550, Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:01:11.018086+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2374","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERC were changed from Dyskeratosis congenita, autosomal dominant 1, MIM# 127550 to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:00:54.848169+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2373","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:00:35.712417+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2373","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TERC: Changed phenotypes: Dyskeratosis congenita, autosomal dominant 1, MIM# 127550, Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T16:00:20.178018+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.114","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TERC were changed from Dyskeratosis congenita, autosomal dominant 1, MIM# 127550 to Dyskeratosis congenita, autosomal dominant 1, MIM# 127550; Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T15:59:52.201290+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: TERC.","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T15:59:43.384256+11:00","panel_name":"Bone Marrow Failure","panel_id":56,"panel_version":"1.113","user_name":"Zornitza Stark","item_type":"entity","text":"edited their review of gene: TERC: Changed phenotypes: Dyskeratosis congenita, autosomal dominant 1, MIM# 127550, Pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 2, MIM# 614743","entity_name":"TERC","entity_type":"gene"},{"created":"2025-03-14T15:58:59.933109+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RNU2-2P.","entity_name":"RNU2-2P","entity_type":"gene"},{"created":"2025-03-14T15:58:47.476981+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.119","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RNU2-2P.","entity_name":"RNU2-2P","entity_type":"gene"},{"created":"2025-03-14T15:58:32.450164+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2373","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: RNU2-2P.","entity_name":"RNU2-2P","entity_type":"gene"},{"created":"2025-03-14T15:58:11.196971+11:00","panel_name":"Prepair 1000+","panel_id":3861,"panel_version":"1.1586","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:57:38.603053+11:00","panel_name":"Fetal anomalies","panel_id":3763,"panel_version":"1.314","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:57:06.861690+11:00","panel_name":"Leukodystrophy - paediatric","panel_id":298,"panel_version":"0.318","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:56:52.090027+11:00","panel_name":"Dystonia - complex","panel_id":290,"panel_version":"0.272","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:56:39.457175+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"1.83","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:56:25.939008+11:00","panel_name":"Genetic Epilepsy","panel_id":202,"panel_version":"1.119","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"},{"created":"2025-03-14T15:56:10.635988+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"1.2373","user_name":"Zornitza Stark","item_type":"entity","text":"Tag non-coding gene tag was added to gene: SNORD118.","entity_name":"SNORD118","entity_type":"gene"}]}