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Cancer Genome Characterization Initiative

Visit the database of genomic characterization data for multiple tumor types.


Gene Info

Gene Information For:Hs. HOXA13, homeobox A13
Sequence ID:NM_000522
RefSeqGene ID:NG_008181
Entrez Gene ID:3209
Ensembl ID:ENSG00000106031

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneHPRDVegaSNPSNP: GeneViewSNP: VarViewAssembliesCancer AberrationsRNAi

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
GUTTMACHER SYNDROME 
HAND-FOOT-UTERUS SYNDROME 

Cytogenetic Location (from UniGene)

Cytogenetic Location:7p15.2Mitelman Breakpoint Data

Chromosomal Position (from UCSC)

Chromosomal Position:7: 27236498 - 27237972

NM_000522 exon info from UCSC:

Transcript StartTranscript EndChromosomal Start Chromosomal End
115632723649827238060
156425142723877427239724

Full-Length MGC Clones for This Gene

IMAGE IdStatusAccession GenBank Def Line
30341785Full LengthBC075791homeobox A13

Protein Similarities Based on Shared Motif Content

Find gene products sharing protein motifs with:  NP_000513  

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_000522 NP_000513 P31271 Homeobox

Related Sequences

 
mRNAGenPeptSwissProt
BC075791 AAH75791 Q6DI00

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens HOXA13 NP_000513 M.musculus Hoxa13 15398 Gene Info NP_032290 99
R.norvegicus Hoxa13 500129   XP_575481 99

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)