{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1448","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1446","results":[{"created":"2021-01-06T21:46:24.590108+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6002","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VCAN were changed from  to Wagner syndrome 1, MIM# 143200","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:46:02.354272+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6001","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VCAN were set to ","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:45:42.601717+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6000","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VCAN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:45:15.061485+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5999","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VCAN: Rating: GREEN; Mode of pathogenicity: None; Publications: 16877430, 22739342, 16636652, 16043844, 32854301, 30657523, 30055036, 29071374, 27667122; Phenotypes: Wagner syndrome 1, MIM# 143200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:44:22.599876+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: VCAN as ready","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:44:22.587856+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: vcan has been classified as Green List (High Evidence).","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:44:20.213598+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.19","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: VCAN were changed from  to Wagner syndrome 1, MIM# 143200","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:44:12.553004+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.18","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: VCAN were set to ","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:44:03.838448+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.17","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: VCAN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:43:55.772957+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: VCAN.","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:43:48.405778+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: VCAN: Rating: GREEN; Mode of pathogenicity: None; Publications: 16877430, 22739342, 16636652, 16043844, 32854301, 30657523, 30055036, 29071374, 27667122; Phenotypes: Wagner syndrome 1, MIM# 143200; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"VCAN","entity_type":"gene"},{"created":"2021-01-06T21:40:38.449682+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF408 as ready","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:40:38.434897+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf408 has been classified as Green List (High Evidence).","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:40:36.035671+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.16","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF408 were changed from  to Exudative vitreoretinopathy 6, MIM# 616468","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:40:23.489651+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.15","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF408 were set to ","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:39:52.426849+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.14","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF408 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:39:41.275298+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF408: Rating: GREEN; Mode of pathogenicity: None; Publications: 23716654, 32530348, 32097476, 32238352, 30998249, 29982478; Phenotypes: Exudative vitreoretinopathy 6, MIM# 616468; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZNF408","entity_type":"gene"},{"created":"2021-01-06T21:36:30.159250+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5999","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CAPN5 as ready","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:36:30.148005+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5999","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: capn5 has been classified as Green List (High Evidence).","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:34:53.310600+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5999","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CAPN5 were changed from  to Vitreoretinopathy, neovascular inflammatory, MIM# 193235","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:34:31.039811+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5998","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CAPN5 were set to ","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:34:11.264969+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5997","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CAPN5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:33:48.940813+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5996","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CAPN5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23055945, 32274441, 31110225, 30986125; Phenotypes: Vitreoretinopathy, neovascular inflammatory, MIM# 193235; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:33:04.137347+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CAPN5 as ready","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:33:04.129068+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: capn5 has been classified as Green List (High Evidence).","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:33:01.732771+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.13","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CAPN5 were changed from  to Vitreoretinopathy, neovascular inflammatory, MIM# 193235","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:32:53.964992+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.12","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CAPN5 were set to ","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:32:45.744725+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.11","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CAPN5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T21:32:34.382112+11:00","panel_name":"Vitreoretinopathy","panel_id":3113,"panel_version":"0.10","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CAPN5: Rating: GREEN; Mode of pathogenicity: None; Publications: 23055945, 32274441, 31110225, 30986125; Phenotypes: Vitreoretinopathy, neovascular inflammatory, MIM# 193235; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"CAPN5","entity_type":"gene"},{"created":"2021-01-06T14:32:12.874414+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"1.0","user_name":"Zornitza Stark","item_type":"panel","text":"promoted panel to version 1.0","entity_name":null,"entity_type":null},{"created":"2021-01-06T14:31:56.863179+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBIAD1 as ready","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:56.855637+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ubiad1 has been classified as Green List (High Evidence).","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:55.525443+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBIAD1 were changed from Corneal dystrophy, Schnyder type, MIM# 121800 to Corneal dystrophy, Schnyder type, MIM# 121800","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:35.313535+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5996","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: UBIAD1 as ready","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:35.301816+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5996","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ubiad1 has been classified as Green List (High Evidence).","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:31.007710+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.77","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBIAD1 were changed from  to Corneal dystrophy, Schnyder type, MIM# 121800","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:31:25.565544+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5996","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: UBIAD1 were changed from  to Corneal dystrophy, Schnyder type, MIM# 121800","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:30:50.349911+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5995","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBIAD1 were set to ","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:30:32.013673+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5994","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBIAD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:30:13.538887+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5993","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UBIAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18176953, 23169578, 31323021, 30785396, 30223810; Phenotypes: Corneal dystrophy, Schnyder type, MIM# 121800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:30:10.971754+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.76","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: UBIAD1 were set to ","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:29:42.871832+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.75","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: UBIAD1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:29:07.968453+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: UBIAD1: Rating: GREEN; Mode of pathogenicity: None; Publications: 18176953, 23169578, 31323021, 30785396, 30223810; Phenotypes: Corneal dystrophy, Schnyder type, MIM# 121800; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"UBIAD1","entity_type":"gene"},{"created":"2021-01-06T14:26:52.313043+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5993","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBI as ready","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:52.304589+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5993","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbi has been classified as Green List (High Evidence).","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:44.070450+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TGFBI as ready","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:44.058748+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tgfbi has been classified as Green List (High Evidence).","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:43.295903+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5993","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBI were changed from  to Corneal dystrophy, multiple types, MONDO:0000764","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:26.652850+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.74","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TGFBI were changed from  to Corneal dystrophy, multiple types, MONDO:0000764","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:22.797004+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5992","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFBI were set to ","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:26:03.999716+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5991","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBI was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:25:45.164428+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5990","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBI: Rating: GREEN; Mode of pathogenicity: None; Publications: 9054935; Phenotypes: Corneal dystrophy, multiple types, MONDO:0000764; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:25:44.514106+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.73","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TGFBI were set to ","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:25:18.612213+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.72","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TGFBI was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:24:49.630026+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TGFBI: Rating: GREEN; Mode of pathogenicity: None; Publications: 9054935; Phenotypes: Corneal dystrophy, multiple types, MONDO:0000764; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TGFBI","entity_type":"gene"},{"created":"2021-01-06T14:22:28.659837+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TCF4 as ready","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:22:28.649395+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tcf4 has been classified as Green List (High Evidence).","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:22:26.462668+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.71","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TCF4 were changed from  to Corneal dystrophy, Fuchs endothelial, 3, MIM# 613267","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:22:02.788789+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.70","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TCF4 were set to ","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:21:32.128934+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.69","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TCF4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:21:03.127692+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Tag STR tag was added to gene: TCF4.","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:20:54.332184+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TCF4: Rating: GREEN; Mode of pathogenicity: Other; Publications: 25722209; Phenotypes: Corneal dystrophy, Fuchs endothelial, 3, MIM# 613267; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"TCF4","entity_type":"gene"},{"created":"2021-01-06T14:18:46.221626+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5990","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TACSTD2 as ready","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:18:46.211905+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5990","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tacstd2 has been classified as Green List (High Evidence).","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:18:38.602799+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5990","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TACSTD2 were changed from  to Corneal dystrophy, gelatinous drop-like, MIM# 204870","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:18:19.583208+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5989","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TACSTD2 were set to ","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:17:57.916083+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5988","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TACSTD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:17:37.872857+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5987","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TACSTD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10192395, 12107443, 12614764, 31666974, 31534795; Phenotypes: Corneal dystrophy, gelatinous drop-like, MIM# 204870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:17:29.794667+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: TACSTD2 as ready","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:17:29.782928+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: tacstd2 has been classified as Green List (High Evidence).","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:16:55.434777+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.68","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: TACSTD2 were changed from  to Corneal dystrophy, gelatinous drop-like, MIM# 204870","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:16:29.888881+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.67","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: TACSTD2 were set to ","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:16:02.248988+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.66","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: TACSTD2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:15:32.475321+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: TACSTD2: Rating: GREEN; Mode of pathogenicity: None; Publications: 10192395, 12107443, 12614764, 31666974, 31534795; Phenotypes: Corneal dystrophy, gelatinous drop-like, MIM# 204870; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"TACSTD2","entity_type":"gene"},{"created":"2021-01-06T14:13:06.348883+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: SLC4A11 as ready","entity_name":"SLC4A11","entity_type":"gene"},{"created":"2021-01-06T14:13:06.336660+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: slc4a11 has been classified as Green List (High Evidence).","entity_name":"SLC4A11","entity_type":"gene"},{"created":"2021-01-06T14:13:04.111998+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.65","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: SLC4A11 were changed from  to Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268; Corneal endothelial dystrophy and perceptive deafness, MIM# 217400; Corneal endothelial dystrophy, autosomal recessive, MIM# 217700","entity_name":"SLC4A11","entity_type":"gene"},{"created":"2021-01-06T14:12:35.502068+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.64","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: SLC4A11 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC4A11","entity_type":"gene"},{"created":"2021-01-06T14:12:06.372101+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: SLC4A11: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268, Corneal endothelial dystrophy and perceptive deafness, MIM# 217400, Corneal endothelial dystrophy, autosomal recessive, MIM# 217700; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal","entity_name":"SLC4A11","entity_type":"gene"},{"created":"2021-01-06T14:09:09.499201+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PRDM5 as ready","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:09:09.491087+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: prdm5 has been classified as Green List (High Evidence).","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:09:06.690094+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.63","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PRDM5 were changed from  to Brittle cornea syndrome 2, MIM# 614170","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:08:36.843416+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.62","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PRDM5 were set to ","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:08:06.708011+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.61","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PRDM5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:07:37.205717+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PRDM5: Rating: GREEN; Mode of pathogenicity: None; Publications: 21664999, 22122778, 26395458, 33120686, 27032025; Phenotypes: Brittle cornea syndrome 2, MIM# 614170; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"PRDM5","entity_type":"gene"},{"created":"2021-01-06T14:04:47.594552+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5987","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF27 as ready","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:47.581193+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5987","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif27 has been classified as Red List (Low Evidence).","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:38.789590+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5987","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF27 as Red List (low evidence)","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:38.781179+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5987","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif27 has been classified as Red List (Low Evidence).","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:15.793535+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KIF27 as ready","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:15.784639+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif27 has been classified as Red List (Low Evidence).","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:12.498730+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: KIF27 as Red List (low evidence)","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T14:04:12.486844+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.245","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: kif27 has been classified as Red List (Low Evidence).","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T12:08:20.229801+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5986","user_name":"Anna Le Fevre","item_type":"entity","text":"reviewed gene: KIF27: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T12:07:31.288239+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.244","user_name":"Anna Le Fevre","item_type":"entity","text":"reviewed gene: KIF27: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: Unknown","entity_name":"KIF27","entity_type":"gene"},{"created":"2021-01-06T11:24:08.783083+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.244","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZEB1 as ready","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:24:08.772359+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.244","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zeb1 has been classified as Amber List (Moderate Evidence).","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:24:06.074206+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.244","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZEB1 were changed from  to Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270; Corneal dystrophy, posterior polymorphous, 3, MIM# 609141; Corpus callosum abnormalities","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:23:38.106431+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.243","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZEB1 were set to ","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:23:09.306810+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.242","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZEB1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZEB1","entity_type":"gene"}]}