View WNT4 gene homepage

General information
Gene symbol WNT4
Gene name wingless-type MMTV integration site family, member 4
Chromosome 1
Chromosomal band p36.23-p35.1
Imprinted Unknown
Genomic reference NG_008974.1
Transcript reference NM_030761.4
Associated with diseases Serkal, Mullerian aplasia and hyperandrogenism
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 1
Unique public DNA variants reported 1
Individuals with public variants 1
Hidden variants 0
Date created May 03, 2013

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 12783
Entrez Gene 54361
PubMed articles WNT4
OMIM - Gene 603490
OMIM - Diseases Serkal (Serkal syndrome)
Mullerian aplasia and hyperandrogenism

Active transcripts




NCBI ID     

NCBI Protein ID     

00022856 1 wingless-type MMTV integration site family, member 4 NM_030761.4 NP_110388.2 1