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Giving unique and meaningful names to every human gene

Core Data Database Links
Approved Symbol + C10orf2  RefSeq IDs +
Approved Name + chromosome 10 open reading frame 2 NM_021830 GenBank  EMBL DDBJ UCSC
HGNC ID + HGNC:1160 Accession Numbers +
Status + Approved AF292004 GenBank  EMBL DDBJ UCSC
Chromosome + 10q24 Mouse Genome Database ID +
Previous Symbols + IOSCA, SCA8 MGI:2137410 MGD ID 
Previous Names + "infantile onset spinocerebellar ataxia (autosomal recessive)" Rat Genome Database ID (mapped data supplied by RGD) +
Aliases + PEO, PEO1, TWINKLE, FLJ21832, TWINL, ATXN8 RGD:1307884 RGD ID 
Name Aliases + "twinkle", "ataxin 8" Entrez Gene ID +
Locus Type + gene with protein product 56652 Gene  Map Viewer 
  CCDS IDs +
Gene Symbol Links CCDS7506.1 CCDS ID 
GENATLAS GeneCards GeneClinics/GeneTests GoPubmed
       
HCOP H-InvDB Treefam wikigenes
 
Ensembl Gene ID +
ENSG00000107815 Ensembl GeneView  UCSC 
Pubmed IDs +
11431692, 10645945, 16135556 PMID  CiteXplore 
Specialist Database Links VEGA IDs +
COSMIC Orphanet:159897
 
OTTHUMG00000018917 VEGA GeneView 
OMIM ID (mapped data supplied by NCBI) +
Locus Specific Database Links 606075 OMIM 
  UCSC ID (mapped data supplied by UCSC) +
uc001ksf.2 UCSC Index 
UniProt ID (mapped data supplied by UniProt) +
  Q96RR1 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.