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WNT4 - Wnt family member 4

Synonym(s) : WNT-4
Previous symbols and names : wingless-type MMTV integration site family, member 4
Type : gene with protein product
Chromosomal location : 1p36.12
OMIM: 603490
HGNC: 12783
UniProtKB: P56705
Genatlas: WNT4
Ensembl: ENSG00000162552
IUPHAR-DB: -
Reactome: P56705
LOVD: WNT4

Diseases list

Disease-causing germline mutation(s) (loss of function) in Müllerian aplasia and hyperandrogenism ORPHA:247768
Disease-causing germline mutation(s) (loss of function) in SERKAL syndrome ORPHA:139466

: Assessed

Gene included in a panel of genes performed as part of a diagnostic test

Additional information

Health care resources for this gene

Diagnostic tests (20)

Research activities on this gene

Specialised Social Services

Eurordis directory

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