The WNT10A gene homepage

General information
Gene symbol WNT10A
Gene name wingless-type MMTV integration site family, member 10A
Chromosome 2
Chromosomal band q35
Imprinted Unknown
Genomic reference NG_012179.1
Transcript reference NM_025216.2
Exon/intron information NM_025216.2 exon/intron table
Associated with diseases OODD, SSPS, STHAG-4
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 135
Unique public DNA variants reported 29
Individuals with public variants 93
Hidden variants 3
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created April 05, 2011
Date last updated October 18, 2021
Version WNT10A:211018

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_025216.2.
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
Homepage URL
HGNC 13829
Entrez Gene 80326
PubMed articles WNT10A
OMIM - Gene 606268
OMIM - Diseases OODD (dysplasia, odontoonychodermal (OODD))
SSPS (Schopf-Schulz-Passarge syndrome (SSPS))
STHAG-4 (agenesis, tooth, selective, type 4 (STHAG-4))
GeneCards WNT10A
GeneTests WNT10A
Orphanet WNT10A

Active transcripts




NCBI ID     

NCBI Protein ID     

00000048 2 wingless-type MMTV integration site family, member 10A NM_025216.2 NP_079492.2 135

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