NONO

non-POU domain containing octamer binding
OMIM: 300084, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green NONO in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Expert list Phenotypes Mental retardation, X-linked, syndromic 34, MIM# 300967
Green NONO in Mendeliome Version 1.2302	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967
Green NONO in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.540	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967
Green NONO in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.63	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Genetic Health Queensland Phenotypes Intellectual developmental disorder, X-linked syndromic 34 - MIM#300967
Green NONO in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.196	0 reviews	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green NHS GMS
Green NONO in Fetal anomalies Version 1.313	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Genomics England PanelApp Expert list Phenotypes Mental retardation, X-linked, syndromic 34, MIM# 300967 Ventricular septal defect (VSD) Pulmonary stenosis Ebstein s anomaly Left ventricular non-compaction cardiomyopathy (LVNC)