The WNT5A gene homepage

General information
Gene symbol WNT5A
Gene name wingless-type MMTV integration site family, member 5A
Chromosome 3
Chromosomal band p21-p14
Imprinted Unknown
Genomic reference NG_031992.1
Transcript reference NM_003392.4
Exon/intron information NM_003392.4 exon/intron table
Associated with diseases DRS, DRS1, ID
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Juliana Mazzeu
Total number of public variants reported 23
Unique public DNA variants reported 21
Individuals with public variants 20
Hidden variants 4
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 May 03, 2013
Date last updated April 19, 2024
Version WNT5A:240419

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_003392.4.
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 https://www.LOVD.nl/WNT5A
HGNC 12784
Entrez Gene 7474
PubMed articles WNT5A
OMIM - Gene 164975
OMIM - Diseases DRS1 (Robinow, autosomal dominant syndrome, type 1 (DRS1))
HGMD WNT5A
GeneCards WNT5A
GeneTests WNT5A
Orphanet WNT5A


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022857 3 transcript variant 1 NM_003392.4 NP_003383.2 23


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