{"count":220257,"next":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1410","previous":"https://panelapp-aus.org/api/v1/activities/?format=json&page=1408","results":[{"created":"2021-02-14T08:11:49.961320+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.175","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CLP1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CLP1","entity_type":"gene"},{"created":"2021-02-14T08:11:23.015589+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Tag founder tag was added to gene: CLP1.","entity_name":"CLP1","entity_type":"gene"},{"created":"2021-02-14T08:11:11.855447+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CLP1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24766809; Phenotypes: Pontocerebellar hypoplasia, type 10, MIM# 615803; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CLP1","entity_type":"gene"},{"created":"2021-02-13T22:04:22.796488+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHMP1A as ready","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:04:22.785594+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chmp1a has been classified as Green List (High Evidence).","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:04:17.798998+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3446","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHMP1A were changed from  to Pontocerebellar hypoplasia, type 8, MIM# 614961","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:03:50.500725+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3445","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHMP1A were set to ","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:03:21.954239+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3444","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHMP1A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:02:46.403599+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CHMP1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23023333; Phenotypes: Pontocerebellar hypoplasia, type 8, MIM# 614961; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:00:29.596319+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHMP1A as ready","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:00:29.585852+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chmp1a has been classified as Red List (Low Evidence).","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T22:00:26.530159+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.240","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHMP1A were changed from  to Pontocerebellar hypoplasia, type 8, MIM# 614961","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:59:57.822292+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.239","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHMP1A were set to ","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:59:21.526136+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.238","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHMP1A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:58:54.288310+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Classified gene: CHMP1A as Red List (low evidence)","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:58:54.277984+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.237","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chmp1a has been classified as Red List (Low Evidence).","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:58:24.562793+11:00","panel_name":"Regression","panel_id":206,"panel_version":"0.236","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CHMP1A: Rating: RED; Mode of pathogenicity: None; Publications: 23023333; Phenotypes: Pontocerebellar hypoplasia, type 8, MIM# 614961; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:57:31.833794+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6365","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHMP1A as ready","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:57:31.823628+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6365","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chmp1a has been classified as Green List (High Evidence).","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:57:23.859059+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6365","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHMP1A were changed from  to Pontocerebellar hypoplasia, type 8, MIM# 614961","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:57:02.193692+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6364","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHMP1A were set to ","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:56:42.380191+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6363","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHMP1A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:56:22.610623+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6362","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CHMP1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23023333; Phenotypes: Pontocerebellar hypoplasia, type 8, MIM# 614961; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:53:10.929546+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CHMP1A as ready","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:53:10.921107+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: chmp1a has been classified as Green List (High Evidence).","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:53:08.087888+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.174","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CHMP1A were changed from  to Pontocerebellar hypoplasia, type 8, MIM# 614961","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:52:45.050243+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.173","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: CHMP1A were set to ","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:51:55.652340+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.172","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CHMP1A was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:51:27.009304+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CHMP1A: Rating: GREEN; Mode of pathogenicity: None; Publications: 23023333; Phenotypes: Pontocerebellar hypoplasia, type 8, MIM# 614961; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"CHMP1A","entity_type":"gene"},{"created":"2021-02-13T21:26:09.170496+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: CASK as ready","entity_name":"CASK","entity_type":"gene"},{"created":"2021-02-13T21:26:09.157816+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: cask has been classified as Green List (High Evidence).","entity_name":"CASK","entity_type":"gene"},{"created":"2021-02-13T21:26:06.945067+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.171","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: CASK were changed from  to Mental retardation and microcephaly with pontine and cerebellar hypoplasia, MIM# 300749","entity_name":"CASK","entity_type":"gene"},{"created":"2021-02-13T21:25:43.773481+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.170","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: CASK was changed from Unknown to Other","entity_name":"CASK","entity_type":"gene"},{"created":"2021-02-13T21:25:13.352536+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: CASK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Mental retardation and microcephaly with pontine and cerebellar hypoplasia, MIM# 300749; Mode of inheritance: Other","entity_name":"CASK","entity_type":"gene"},{"created":"2021-02-13T21:24:24.541096+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRF1 as ready","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:24:24.531989+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brf1 has been classified as Green List (High Evidence).","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:24:20.219044+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3443","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRF1 were changed from  to Cerebellofaciodental syndrome, MIM# 616202","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:23:54.482779+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3442","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRF1 were set to ","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:23:23.536285+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3441","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:22:50.466558+11:00","panel_name":"Intellectual disability syndromic and non-syndromic","panel_id":250,"panel_version":"0.3440","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BRF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25561519, 25561519, 27748960; Phenotypes: Cerebellofaciodental syndrome, MIM# 616202; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:22:14.099286+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6362","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRF1 as ready","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:22:14.088250+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6362","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brf1 has been classified as Green List (High Evidence).","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:22:04.439065+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6362","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRF1 were changed from  to Cerebellofaciodental syndrome, MIM# 616202","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:21:46.018639+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6361","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRF1 were set to ","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:21:26.787174+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6360","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:21:07.179832+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6359","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BRF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25561519, 25561519, 27748960; Phenotypes: Cerebellofaciodental syndrome, MIM# 616202; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:20:12.890780+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: BRF1 as ready","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:20:12.879756+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: brf1 has been classified as Green List (High Evidence).","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:20:09.751195+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.169","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: BRF1 were changed from  to Cerebellofaciodental syndrome, MIM# 616202","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:19:45.424326+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.168","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: BRF1 were set to ","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:19:15.819024+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.167","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: BRF1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T21:18:42.813152+11:00","panel_name":"Cerebellar and Pontocerebellar Hypoplasia","panel_id":72,"panel_version":"0.166","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: BRF1: Rating: GREEN; Mode of pathogenicity: None; Publications: 25561519, 25561519, 27748960; Phenotypes: Cerebellofaciodental syndrome, MIM# 616202; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"BRF1","entity_type":"gene"},{"created":"2021-02-13T20:25:01.074731+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:25:01.062806+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:24:58.135424+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.100","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHODH were changed from POADS = MILLER; POSTAXIAL ACROFACIAL DYSOSTOSIS to Miller syndrome, MIM# 263750","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:24:30.494603+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.99","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:23:19.679771+11:00","panel_name":"Clefting disorders","panel_id":3368,"panel_version":"0.98","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DHODH: Rating: GREEN; Mode of pathogenicity: None; Publications: 19915526, 20220176, 33262786, 27370710; Phenotypes: Miller syndrome, MIM# 263750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:22:40.763091+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:22:40.751540+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:22:25.826109+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.24","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHODH were changed from  to Miller syndrome, MIM# 263750","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:22:02.031156+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:21:26.967986+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DHODH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:20:57.869160+11:00","panel_name":"Pierre Robin Sequence","panel_id":160,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DHODH: Rating: GREEN; Mode of pathogenicity: None; Publications: 19915526, 20220176, 33262786, 27370710; Phenotypes: Miller syndrome, MIM# 263750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:20:17.240665+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6359","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:20:17.230181+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6359","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:20:07.673302+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6359","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHODH were changed from  to Miller syndrome, MIM# 263750","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:19:45.376085+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6358","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:19:16.501313+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6357","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DHODH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:18:57.280924+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6356","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DHODH: Rating: GREEN; Mode of pathogenicity: None; Publications: 19915526, 20220176, 33262786, 27370710; Phenotypes: Miller syndrome, MIM# 263750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:18:02.437567+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: DHODH as ready","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:18:02.426834+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: dhodh has been classified as Green List (High Evidence).","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:17:59.797535+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.23","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: DHODH were changed from  to Miller syndrome, MIM# 263750","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:17:32.381527+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.22","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: DHODH were set to ","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:17:04.010430+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.21","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: DHODH was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:16:13.728302+11:00","panel_name":"Mandibulofacial Acrofacial dysostosis","panel_id":136,"panel_version":"0.20","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: DHODH: Rating: GREEN; Mode of pathogenicity: None; Publications: 19915526, 20220176, 33262786, 27370710; Phenotypes: Miller syndrome, MIM# 263750; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"DHODH","entity_type":"gene"},{"created":"2021-02-13T20:12:32.218383+11:00","panel_name":"Glycogen Storage Diseases","panel_id":106,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: AGL as ready","entity_name":"AGL","entity_type":"gene"},{"created":"2021-02-13T20:12:32.206830+11:00","panel_name":"Glycogen Storage Diseases","panel_id":106,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: agl has been classified as Green List (High Evidence).","entity_name":"AGL","entity_type":"gene"},{"created":"2021-02-13T20:12:29.700460+11:00","panel_name":"Glycogen Storage Diseases","panel_id":106,"panel_version":"0.31","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: AGL were changed from  to Glycogen storage disease IIIa and IIIb, MIM# 232400","entity_name":"AGL","entity_type":"gene"},{"created":"2021-02-13T20:11:57.270512+11:00","panel_name":"Glycogen Storage Diseases","panel_id":106,"panel_version":"0.30","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: AGL was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"AGL","entity_type":"gene"},{"created":"2021-02-13T20:11:20.789775+11:00","panel_name":"Glycogen Storage Diseases","panel_id":106,"panel_version":"0.29","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: AGL: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Glycogen storage disease IIIa and IIIb, MIM# 232400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"AGL","entity_type":"gene"},{"created":"2021-02-13T20:08:23.690161+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"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":"2021-02-13T20:07:45.523418+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6356","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ITGB4 as ready","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:07:45.515402+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6356","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: itgb4 has been classified as Green List (High Evidence).","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:07:37.249423+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6356","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ITGB4 were changed from  to Epidermolysis bullosa of hands and feet, MIM# 131800; Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650; Epidermolysis bullosa, junctional, with pyloric atresia, MIM# 226730","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:07:16.966129+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6355","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ITGB4 were set to ","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:06:55.838393+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6354","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ITGB4 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:06:36.995555+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6353","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ITGB4: Rating: GREEN; Mode of pathogenicity: None; Publications: 11328943, 9670011, 33225458, 30079450, 29380424, 29198538, 28557647; Phenotypes: Epidermolysis bullosa of hands and feet, MIM# 131800, Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650, Epidermolysis bullosa, junctional, with pyloric atresia, MIM# 226730; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:05:26.399960+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: ITGB4 as ready","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:05:26.388339+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: itgb4 has been classified as Green List (High Evidence).","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:05:22.522669+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.87","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: ITGB4 were changed from  to Epidermolysis bullosa of hands and feet, MIM# 131800; Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650; Epidermolysis bullosa, junctional, with pyloric atresia, MIM# 226730","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:04:52.100782+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.86","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: ITGB4 were set to ","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:04:17.951361+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.85","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: ITGB4 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T20:03:44.656035+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: ITGB4: Rating: GREEN; Mode of pathogenicity: None; Publications: 11328943, 9670011, 33225458, 30079450, 29380424, 29198538, 28557647; Phenotypes: Epidermolysis bullosa of hands and feet, MIM# 131800, Epidermolysis bullosa, junctional, non-Herlitz type, MIM# 226650, Epidermolysis bullosa, junctional, with pyloric atresia, MIM# 226730; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal","entity_name":"ITGB4","entity_type":"gene"},{"created":"2021-02-13T19:59:31.889535+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6353","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMA3 as ready","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:59:31.879056+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6353","user_name":"Zornitza Stark","item_type":"entity","text":"Gene: lama3 has been classified as Green List (High Evidence).","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:59:19.111289+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6353","user_name":"Zornitza Stark","item_type":"entity","text":"Phenotypes for gene: LAMA3 were changed from  to Epidermolysis bullosa, generalized atrophic benign, MIM# 226650; Epidermolysis bullosa, junctional, Herlitz type, MIM# 226700","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:59:00.366242+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6352","user_name":"Zornitza Stark","item_type":"entity","text":"Publications for gene: LAMA3 were set to ","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:58:39.673539+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6351","user_name":"Zornitza Stark","item_type":"entity","text":"Mode of inheritance for gene: LAMA3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:58:13.069499+11:00","panel_name":"Mendeliome","panel_id":137,"panel_version":"0.6350","user_name":"Zornitza Stark","item_type":"entity","text":"reviewed gene: LAMA3: Rating: GREEN; Mode of pathogenicity: None; Publications: 7633458, 8530087, 11810295, 10366601; Phenotypes: Epidermolysis bullosa, generalized atrophic benign, MIM# 226650, Epidermolysis bullosa, junctional, Herlitz type, MIM# 226700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal","entity_name":"LAMA3","entity_type":"gene"},{"created":"2021-02-13T19:57:21.803614+11:00","panel_name":"Epidermolysis bullosa","panel_id":101,"panel_version":"0.84","user_name":"Zornitza Stark","item_type":"entity","text":"Marked gene: LAMA3 as ready","entity_name":"LAMA3","entity_type":"gene"}]}