09 Jan 2024
Intellectual disability - microarray and sequencing v5.388
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.388
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.387
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.388
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.388
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.388
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.387
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from None to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.387
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments to None
09 Jan 2024
Intellectual disability - microarray and sequencing v5.386
RARB
Achchuthan Shanmugasundram Publications for gene: RARB were set to 17506106; 24075189; 25457163; 27120018; 30281527; 30880327
09 Jan 2024
Intellectual disability - microarray and sequencing v5.386
RARB
Achchuthan Shanmugasundram Publications for gene: RARB were set to 17506106; 24075189; 25457163; 27120018; 30281527; 30880327
09 Jan 2024
Intellectual disability - microarray and sequencing v5.386
RARB
Achchuthan Shanmugasundram Publications for gene: RARB were set to 17506106; 24075189; 25457163; 27120018; 30281527; 30880327
09 Jan 2024
Intellectual disability - microarray and sequencing v5.385
RARB
Achchuthan Shanmugasundram Publications for gene: RARB were set to 17506106; 24075189; 25457163; 27120018; 30281527; 30880327
09 Jan 2024
Intellectual disability - microarray and sequencing v5.385
RARB
Achchuthan Shanmugasundram Publications for gene: RARB were set to 24075189
09 Jan 2024
Intellectual disability - microarray and sequencing v5.384
RARB
Achchuthan Shanmugasundram Phenotypes for gene: RARB were changed from Microphthalmia, syndromic 12, OMIM:615524; neurodevelopmental disorder, MONDO:0700092 to Microphthalmia, syndromic 12, OMIM:615524; neurodevelopmental disorder, MONDO:0700092
09 Jan 2024
Intellectual disability - microarray and sequencing v5.384
RARB
Achchuthan Shanmugasundram Phenotypes for gene: RARB were changed from Microphthalmia, syndromic 12, OMIM:615524; neurodevelopmental disorder, MONDO:0700092 to Microphthalmia, syndromic 12, OMIM:615524; neurodevelopmental disorder, MONDO:0700092
09 Jan 2024
Intellectual disability - microarray and sequencing v5.383
RARB
Achchuthan Shanmugasundram Phenotypes for gene: RARB were changed from MICROPHTHALMIA AND DIAPHRAGMATIC HERNIA to Microphthalmia, syndromic 12, OMIM:615524; neurodevelopmental disorder, MONDO:0700092
09 Jan 2024
Intellectual disability - microarray and sequencing v5.381
RARB
Achchuthan Shanmugasundram Mode of pathogenicity for gene: RARB was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
06 Dec 2022
Intellectual disability - microarray and sequencing v4.2
RARB
Zornitza Stark reviewed gene: RARB: Rating: GREEN; Mode of pathogenicity: None; Publications: 30880327, 30281527, 24075189, 27120018, 25457163, 17506106; Phenotypes: Microphthalmia, syndromic 12, MIM# 615524, Neurodevelopmental disorder; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
29 Nov 2022
Intellectual disability - microarray and sequencing v3.1771
RARB
Dmitrijs Rots reviewed gene: RARB: Rating: ; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 27120018; Phenotypes: Intellectual Disability with Progressive Motor Impairment; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
29 Sep 2018
Intellectual disability - microarray and sequencing v2.468
RARB
Louise Daugherty Source Victorian Clinical Genetics Services was added to RARB.
02 Aug 2017
Intellectual disability - microarray and sequencing
RARB
BRIDGE consortium edited their review of RARB
27 Jul 2017
Intellectual disability - microarray and sequencing
RARB
BRIDGE consortium edited their review of RARB
19 Jul 2017
Intellectual disability - microarray and sequencing
RARB
BRIDGE consortium reviewed RARB