Homo sapiens Protein: TCTA
Summary
InnateDB Protein IDBP-34811.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TCTA
Protein Name T-cell leukemia translocation altered gene
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000273590
InnateDB Gene IDBG-34809 (TCTA)
Protein Structure
UniProt Annotation
Function May be required for cellular fusion during osteoclastogenesis. {ECO:0000269PubMed:19560569}.
Subcellular Localization Membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}.
Disease Associations Note=A chromosomal aberration involving TCTA is associated with T-cell acute lymphoblastic leukemia (T-ALL). Translocation t(1;3)(p34;p21).
Tissue Specificity Ubiquitous. Highest level of expression in kidney. Present in monocytes, osteoclasts, macrophages, synoviocytes and synovial lining cells (at protein level). {ECO:0000269PubMed:7728759}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR016560 T-cell leukemia translocation-altered gene protein
PFAM PF15128
PRINTS
PIRSF PIRSF009935
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P57738
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 6988
UniGene Hs.739127
RefSeq NP_071503
HUGO HGNC:11692
OMIM 600690
CCDS CCDS2796
HPRD 15977
IMGT
EMBL AC104452 AK311839 BC005157 CR457411 L41143
GenPept AAA97514 AAH05157 BAG34781 CAG33692