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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + WNT7B  RefSeq IDs +
Approved Name + wingless-type MMTV integration site family, member 7B NM_058238 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:12787 Accession Numbers +
Status + Approved AF416743 GenBank  EMBL DDBJ UCSC
Chromosome + 22q13 Mouse Genome Database ID +
Previous Symbols +   MGI:98962 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases +   RGD:1311441 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 7477 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS33667.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
8168088, 9284940, 11562755 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000154636 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
COSMIC
 
ENSG00000188064 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 601967 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc003bgo.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  P56706 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.