SLC6A4

solute carrier family 6 member 4
OMIM: 182138, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SLC6A4 in Mendeliome


Version 1.3795

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Autism spectrum disorder MONDO:0005258
Tags
  • disputed

Red SLC6A4 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.507

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • autism spectrum disorder MONDO:0005258
  • {Obsessive-compulsive disorder}, MIM# 164230
Tags
  • disputed