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WNT7A

Wnt family member 7A
2 disorders 1 causative 1 untyped 3p25.1 gene with protein product
HGNC:12786MonarchNCBI Gene 7476ENSG00000154764UniProt O00755OMIM 601570

Aliases: Wnt-7a.

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
Fuhrmann Syndrome causative partial loss of function
mechanism: Partial Loss of WNT7A Function
Humeroradial Synostosis untyped
Causative

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