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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + WNT9A  RefSeq IDs +
Approved Name + wingless-type MMTV integration site family, member 9A NM_003395 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:12778 Accession Numbers +
Status + Approved AB060283 GenBank  EMBL DDBJ UCSC
Chromosome + 1q42 Mouse Genome Database ID +
Previous Symbols + WNT14 MGI:2446084 MGD ID 
Previous Names + "wingless-type MMTV integration site family, member 14" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases +   RGD:1305018 RGD ID 
Name Aliases +   Entrez Gene ID +
Locus Type + gene with protein product 7483 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS31045.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Pubmed IDs +
9441749 PMID  CiteXplore 
VEGA IDs +
OTTHUMG00000037592 VEGA GeneView 
Specialist Database Links Ensembl ID (mapped data supplied by Ensembl) +
COSMIC
 
ENSG00000143816 Ensembl GeneView  UCSC 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 602863 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc001hri.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  O14904 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.