INTS6

integrator complex subunit 6
OMIM: 604331, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green INTS6 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 1.12

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 78, MIM# 621627

Green INTS6 in Mendeliome


Version 2.278

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 78, MIM# 621627

Green INTS6 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.44

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 78, MIM# 621627