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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + WNT11  RefSeq IDs +
Approved Name + wingless-type MMTV integration site family, member 11 NM_004626 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:12776 Accession Numbers +
Status + Approved Y12692 GenBank  EMBL DDBJ UCSC
Chromosome + 11q13.5 Mouse Genome Database ID +
Previous Symbols +   MGI:101948 MGD ID 
Previous Names +   Rat Genome Database ID (mapped data supplied by RGD) +
Aliases +   RGD:621463 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 7481 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS8242.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
9757009 PMID  CiteXplore 
Ensembl ID (mapped data supplied by Ensembl) +
ENSG00000085741 Ensembl GeneView  UCSC 
Specialist Database Links OMIM ID (mapped data supplied by NCBI) +
COSMIC
 
603699 OMIM 
UCSC ID (mapped data supplied by UCSC) +
Locus Specific Database Links uc001oxe.2 UCSC Index 
  UniProt ID (mapped data supplied by UniProt) +
O96014 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.