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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + WNT9B  RefSeq IDs +
Approved Name + wingless-type MMTV integration site family, member 9B NM_003396 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:12779 Accession Numbers +
Status + Approved AF028703 GenBank  EMBL DDBJ UCSC
Chromosome + 17q21 Mouse Genome Database ID +
Previous Symbols + WNT15 MGI:1197020 MGD ID 
Previous Names + "wingless-type MMTV integration site family, member 15" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + WNT14B RGD:1309574 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 7484 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS11506.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
9441749, 11713592 PMID  CiteXplore 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000158955 Ensembl GeneView  UCSC 
Specialist Database Links OMIM ID (mapped data supplied by NCBI) +
COSMIC
 
602864 OMIM 
UCSC ID (mapped data supplied by UCSC) +
Locus Specific Database Links uc002ikw.1 UCSC Index 
  UniProt ID (mapped data supplied by UniProt) +
O14905 UniProt  UCSC 
 

See Column definitions for descriptions of the various data fields. Also see our custom downloads page for bulk access to our data

 


The work of the HGNC is supported by NHGRI grant P41 HG003345, the UK Medical Research Council and the Wellcome Trust.