RBL2

RB transcriptional corepressor like 2
OMIM: 180203, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red RBL2 in Cerebellar and Pontocerebellar Hypoplasia Level 2: Neurology and neurodevelopmental disorders Version 1.78	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Severe motor and cognitive impairment Intellectual disability Brunet-Wagner neurodevelopmental syndrome MIM#619690
Green RBL2 in Mendeliome Version 1.2302	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Intellectual disability Brunet-Wagner neurodevelopmental syndrome, MIM# 619690
Amber RBL2 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Severe motor and cognitive impairment Intellectual disability Brunet-Wagner neurodevelopmental syndrome MIM#619690
Amber RBL2 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.108 Component of the following Super Panels: Progressive Neurological Conditions	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Literature Phenotypes Brunet-Wagner neurodevelopmental syndrome, MIM# 619690
Green RBL2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Intellectual disability Brunet-Wagner neurodevelopmental syndrome MIM#619690