1. Genes and Genomic Entities
  2. SLC26A7

SLC26A7

solute carrier family 26 member 7
OMIM: 608479, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green SLC26A7 in Congenital hypothyroidism

Level 3: Thyroid disorders
Level 2: Endocrine disorders
Version 2.18
Latest signed off version: v2.2 (25 Feb 2020)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • East of England GLH
Phenotypes
  • Primary congenital hypothyroidism (dyshormonogenesis)
Tags
  • gene-checked