The WNT9B gene homepage

General information
Gene symbol WNT9B
Gene name wingless-type MMTV integration site family, member 9B
Chromosome 17
Chromosomal band q21
Imprinted Unknown
Genomic reference NG_029164.3
Transcript reference NM_003396.1
Exon/intron information NM_003396.1 exon/intron table
Associated with diseases -
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 10
Unique public DNA variants reported 10
Individuals with public variants 4
Hidden variants -
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated May 05, 2025
Version WNT9B:250505

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_003396.1.
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/WNT9B
HGNC HGNC:12779
Entrez Gene 7484
PubMed articles WNT9B
OMIM - Gene 602864
HGMD WNT9B
GeneCards WNT9B
NIH Genetic Testing Registry WNT9B
Orphanet WNT9B


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00022865 17 wingless-type MMTV integration site family, member 9B NM_003396.1 NP_003387.1 10


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