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SLC9A3

solute carrier family 9 member A3
3 disorders 1 susceptibility 1 causative 1 no genetic record 5p15.33 gene with protein product
HGNC:11073MonarchNCBI Gene 6550ENSG00000066230UniProt P48764OMIM 182307

Previous symbols: NHE3. Aliases: NHE-3.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Congenital Bilateral Absence of Vas Deferens susceptibility
Congenital Sodium Diarrhea causative germline
mechanism: Loss of NHE3-Mediated Apical Sodium/Proton Exchange
subtype: Classic non-syndromic CSD
scoped to subtype: Classic non-syndromic CSD
Traveler's Diarrhea no genetic record
mechanism: Inhibition of NHE3-mediated epithelial sodium absorption
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.