RHAG

Rh associated glycoprotein

2 disorders 2 causative 6p12.3 gene with protein product

HGNC:10006 Monarch NCBI Gene 6005 ENSG00000112077 UniProt Q02094 OMIM 180297

Aliases: RH50A, CD241, SLC42A1.

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.

Disorder	Relationship	Where the gene appears
Overhydrated Hereditary Stomatocytosis	causative germline gain of function	mechanism: RHAG Transmembrane Missense Substitution
Rh Deficiency Syndrome	causative

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