NCOA3

nuclear receptor coactivator 3
OMIM: 601937, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NCOA3 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • non-syndromic hearing loss

Red NCOA3 in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.63

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Non-syndromic hearing loss