SLC9A6 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLC9A6 wild-type allele is located in the vicinity of Xq26.3 and is approximately 73 kb in length. This allele, which encodes sodium/hydrogen exchanger 6 protein, is involved in the regulation of ion transport across membranes of early and recycling endosomes. Mutation of the gene is associated with X-linked syndromic cognitive disability, Christianson type.

**Synonyms:** - KIAA0267 - MRSA - MRXSCH - NHE6 - Solute Carrier Family 9 (Sodium/Hydrogen Exchanger), Isoform 6 Gene - Solute Carrier Family 9 (Sodium/Hydrogen Exchanger), Member 6 Gene - Solute Carrier Family 9 Member A6 wt Allele - Solute Carrier Family 9, Subfamily A (NHE6, Cation Proton Antiporter 6), Member 6 Gene