NSD2

nuclear receptor binding SET domain protein 2
OMIM: 602952, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red NSD2 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.389	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Rauch-Steindl syndrome, MIM#619695
Green NSD2 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Rauch-Steindl syndrome, MIM# 619695 Microcephaly intellectual disability Neurodevelopmental disorder, NSD2-associated, GoF, MONDO:0700092
Green NSD2 in Microcephaly Level 2: Dysmorphic and congenital abnormality syndromes Version 1.295	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Rauch-Steindl syndrome, MIM# 619695 Microcephaly intellectual disability
Green NSD2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Genetic Health Queensland Phenotypes Rauch-Steindl syndrome, MIM# 619695 Microcephaly intellectual disability Neurodevelopmental disorder, NSD2-associated, GoF, MONDO:0700092
Green NSD2 in Fetal anomalies Version 1.313	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Rauch-Steindl syndrome, MIM# 619695