{"count":220314,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1449","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1447","results":[{"created":"2021-01-06T11:22:42.142368+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.241","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: ZEB1 as Amber List (moderate evidence)","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:22:42.134366+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.241","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":"2021-01-06T11:22:15.461793+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Tag SV/CNV tag was added to gene: ZEB1.","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:22:03.238897+11:00","panel_name":"Callosome","panel_id":205,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZEB1: Rating: AMBER; Mode of pathogenicity: None; Publications: 24780443, 28284480, 28742278; Phenotypes: Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270, Corneal dystrophy, posterior polymorphous, 3, MIM# 609141, Corpus  callosum abnormalities; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:18:34.694459+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5986","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZEB1 as ready","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:18:34.683657+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5986","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zeb1 has been classified as Green List (High Evidence).","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:18:24.282067+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5986","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","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:18:04.589855+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5985","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZEB1 were set to ","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:17:40.994806+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5984","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"},{"created":"2021-01-06T11:16:49.820824+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5983","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZEB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 16252232, 20036349, 26622166; Phenotypes: Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270, Corneal dystrophy, posterior polymorphous, 3, MIM# 609141; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:16:02.588279+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZEB1 as ready","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:16:02.576693+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.60","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: zeb1 has been classified as Green List (High Evidence).","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:15:59.758969+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.60","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","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:15:33.015701+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.59","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZEB1 were set to ","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:15:05.640946+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.58","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"},{"created":"2021-01-06T11:14:36.458084+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZEB1: Rating: GREEN; Mode of pathogenicity: None; Publications: 16252232, 20036349, 26622166; Phenotypes: Corneal dystrophy, Fuchs endothelial, 6, MIM# 613270, Corneal dystrophy, posterior polymorphous, 3, MIM# 609141; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"ZEB1","entity_type":"gene"},{"created":"2021-01-06T11:11:45.186223+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5983","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF469 as ready","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:11:45.177670+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5983","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf469 has been classified as Green List (High Evidence).","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:11:37.378353+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5983","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF469 were changed from  to Brittle cornea syndrome 1, MIM# 229200","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:11:18.466005+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5982","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF469 were set to ","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:10:57.139466+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5981","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF469 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:10:36.675990+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5980","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF469: Rating: GREEN; Mode of pathogenicity: None; Publications: 18452888, 19661234, 20938016, 21664999, 32671420; Phenotypes: Brittle cornea syndrome 1, MIM# 229200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:09:41.997882+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ZNF469 as ready","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:09:41.987491+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: znf469 has been classified as Green List (High Evidence).","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:09:38.893418+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.57","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ZNF469 were changed from  to Brittle cornea syndrome 1, MIM# 229200","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:09:11.185364+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.56","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ZNF469 were set to ","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:08:35.712055+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.55","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ZNF469 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:08:06.386158+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ZNF469: Rating: GREEN; Mode of pathogenicity: None; Publications: 18452888, 19661234, 20938016, 21664999, 32671420; Phenotypes: Brittle cornea syndrome 1, MIM# 229200; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"ZNF469","entity_type":"gene"},{"created":"2021-01-06T11:05:02.649346+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5980","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIKFYVE as ready","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:05:02.641967+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5980","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pikfyve has been classified as Green List (High Evidence).","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:04:54.159804+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5980","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIKFYVE were changed from  to Corneal fleck dystrophy, MIM# 121850","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:04:33.109840+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5979","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIKFYVE were set to ","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:04:07.531544+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5978","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PIKFYVE was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:03:47.298223+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5977","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PIKFYVE: Rating: GREEN; Mode of pathogenicity: None; Publications: 15902656, 23288988, 26396486; Phenotypes: Corneal fleck dystrophy, MIM# 121850; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:03:00.782228+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: PIKFYVE as ready","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:03:00.770969+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: pikfyve has been classified as Green List (High Evidence).","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:02:55.664313+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.54","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: PIKFYVE were changed from  to Corneal fleck dystrophy, MIM# 121850","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:02:28.473396+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.53","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: PIKFYVE were set to ","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:02:00.085702+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.52","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: PIKFYVE was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T11:01:29.007498+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: PIKFYVE: Rating: GREEN; Mode of pathogenicity: None; Publications: 15902656, 23288988, 26396486; Phenotypes: Corneal fleck dystrophy, MIM# 121850; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"PIKFYVE","entity_type":"gene"},{"created":"2021-01-06T07:23:37.500029+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5977","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OVOL2 as ready","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:23:37.491828+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5977","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ovol2 has been classified as Green List (High Evidence).","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:23:30.295122+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5977","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OVOL2 were changed from  to Corneal dystrophy, posterior polymorphous, 1, MIM# 122000","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:23:11.305238+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5976","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OVOL2 were set to ","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:22:51.758011+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5975","user_name":"Zornitza Stark","item_type":"entity","text":"Tag 5'UTR tag was added to gene: OVOL2.","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:22:39.471147+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5975","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OVOL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:22:20.084419+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5974","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OVOL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26749309; Phenotypes: Corneal dystrophy, posterior polymorphous, 1, MIM# 122000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:21:29.583335+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: OVOL2 as ready","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:21:29.571725+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: ovol2 has been classified as Green List (High Evidence).","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:21:26.606561+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.51","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: OVOL2 were changed from  to Corneal dystrophy, posterior polymorphous, 1, MIM# 122000","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:20:57.553425+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.50","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: OVOL2 were set to ","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:20:31.011824+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.49","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: OVOL2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:20:05.415368+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Tag 5'UTR tag was added to gene: OVOL2.","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:19:53.489813+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: OVOL2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26749309; Phenotypes: Corneal dystrophy, posterior polymorphous, 1, MIM# 122000; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"OVOL2","entity_type":"gene"},{"created":"2021-01-06T07:16:39.869953+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5974","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT3 as ready","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:16:39.859558+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5974","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt3 has been classified as Green List (High Evidence).","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:16:31.244483+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5974","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT3 were changed from  to Meesmann corneal dystrophy 2, MIM# 618767","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:16:13.628002+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5973","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT3 were set to ","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:15:54.973261+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5972","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:15:34.569356+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5971","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9171831, 16227835, 18806880, 26788030; Phenotypes: Meesmann corneal dystrophy 2, MIM# 618767; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:14:48.281547+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5971","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCN as ready","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:14:48.270472+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5971","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcn has been classified as Green List (High Evidence).","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:14:42.051943+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: KRT3 as ready","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:14:42.043551+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: krt3 has been classified as Green List (High Evidence).","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:14:39.765096+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.48","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: KRT3 were changed from  to Meesmann corneal dystrophy 2, MIM# 618767","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:14:12.417392+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.47","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: KRT3 were set to ","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:13:44.699719+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.46","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: KRT3 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:13:15.901578+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.45","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: KRT3: Rating: GREEN; Mode of pathogenicity: None; Publications: 9171831, 16227835, 18806880, 26788030; Phenotypes: Meesmann corneal dystrophy 2, MIM# 618767; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"KRT3","entity_type":"gene"},{"created":"2021-01-06T07:05:44.901665+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5971","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCN were changed from  to Corneal dystrophy, congenital stromal, MIM# 610048","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:05:15.476274+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5970","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCN were set to ","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:04:50.395697+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5969","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DCN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:04:32.114092+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5968","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DCN: Rating: GREEN; Mode of pathogenicity: None; Publications: 15671264, 16935612, 21993463, 24413633, 26828927; Phenotypes: Corneal dystrophy, congenital stromal, MIM# 610048; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:03:39.204072+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DCN as ready","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:03:39.192479+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dcn has been classified as Green List (High Evidence).","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:03:33.752266+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.44","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DCN were changed from  to Corneal dystrophy, congenital stromal, MIM# 610048","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:03:06.937426+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.43","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DCN were set to ","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:02:39.587529+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.42","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DCN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T07:02:09.994374+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DCN: Rating: GREEN; Mode of pathogenicity: None; Publications: 15671264, 16935612, 21993463, 24413633, 26828927; Phenotypes: Corneal dystrophy, congenital stromal, MIM# 610048; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"DCN","entity_type":"gene"},{"created":"2021-01-06T06:58:30.228779+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5968","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL8A2 as ready","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:58:30.217152+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5968","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col8a2 has been classified as Green List (High Evidence).","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:58:21.330971+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5968","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL8A2 were changed from  to Corneal dystrophy, Fuchs endothelial, 1, MIM# 136800; Corneal dystrophy, posterior polymorphous 2, MIM# 609140","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:58:02.570977+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5967","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL8A2 were set to ","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:57:31.581244+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5966","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL8A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:57:12.011357+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5965","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL8A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11689488, 15914606, 18024822, 18464802; Phenotypes: Corneal dystrophy, Fuchs endothelial, 1, MIM# 136800, Corneal dystrophy, posterior polymorphous 2, MIM# 609140; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:56:06.146739+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL8A2 as ready","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:56:06.135480+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col8a2 has been classified as Green List (High Evidence).","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:56:03.593837+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.41","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL8A2 were changed from  to Corneal dystrophy, Fuchs endothelial, 1, MIM# 136800; Corneal dystrophy, posterior polymorphous 2, MIM# 609140","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:55:35.734285+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.40","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL8A2 were set to ","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:55:01.527050+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.39","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL8A2 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:54:32.405127+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL8A2: Rating: GREEN; Mode of pathogenicity: None; Publications: 11689488, 15914606, 18024822, 18464802; Phenotypes: Corneal dystrophy, Fuchs endothelial, 1, MIM# 136800, Corneal dystrophy, posterior polymorphous 2, MIM# 609140; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL8A2","entity_type":"gene"},{"created":"2021-01-06T06:52:01.278212+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: COL17A1 as ready","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-06T06:52:01.253797+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: col17a1 has been classified as Green List (High Evidence).","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-06T06:51:57.362337+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.38","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: COL17A1 were changed from  to Epithelial recurrent erosion dystrophy, MIM# 122400","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-06T06:51:28.944106+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.37","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: COL17A1 were set to ","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-06T06:50:33.722845+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.36","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: COL17A1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-06T06:50:03.210779+11:00","panel_name":"Corneal Dystrophy","panel_id":91,"panel_version":"0.35","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: COL17A1: Rating: GREEN; Mode of pathogenicity: None; Publications: 27309958, 29708937, 25676728; Phenotypes: Epithelial recurrent erosion dystrophy, MIM# 122400; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted","entity_name":"COL17A1","entity_type":"gene"},{"created":"2021-01-05T22:08:54.145929+11:00","panel_name":"Usher Syndrome","panel_id":3086,"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":"2021-01-05T21:50:32.407586+11:00","panel_name":"Congenital Diarrhoea","panel_id":89,"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":"2021-01-05T21:22:59.741297+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5965","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: STX3 as ready","entity_name":"STX3","entity_type":"gene"},{"created":"2021-01-05T21:22:59.730153+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.5965","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: stx3 has been classified as Green List (High Evidence).","entity_name":"STX3","entity_type":"gene"}]}