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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + WNT10B  RefSeq IDs +
Approved Name + wingless-type MMTV integration site family, member 10B NM_003394 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:12775 Accession Numbers +
Status + Approved X97057 GenBank  EMBL DDBJ UCSC
Chromosome + 12q13 Mouse Genome Database ID +
Previous Symbols +   MGI:108061 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + WNT-12, SHFM6 RGD:1304988 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 7480 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS8775.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
9121776, 9284937, 18515319 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000150734 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
COSMIC Orphanet:18356
 
ENSG00000169884 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 601906 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc001rss.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  O00744 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.