Homo sapiens Gene: TGM5
Summary
InnateDB Gene IDBG-8322.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TGM5
Gene Name transglutaminase 5
Synonyms TGASE5; TGASEX; TGM6; TGMX; TGX
Species Homo sapiens
Ensembl Gene ENSG00000104055
Encoded Proteins
transglutaminase 5
transglutaminase 5
transglutaminase 5
transglutaminase 5
transglutaminase 5
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the transglutaminase family. The encoded protein catalyzes formation of protein cross-links between glutamine and lysine residues, often resulting in stabilization of protein assemblies. This reaction is calcium dependent. Mutations in this gene have been associated with acral peeling skin syndrome. [provided by RefSeq, Oct 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 15:43232595-43266857
Strand Reverse strand
Band q15.2
Transcripts
ENST00000220420 ENSP00000220420
ENST00000349114 ENSP00000220419
ENST00000396996
ENST00000563838
ENST00000610827 ENSP00000479732
ENST00000622115 ENSP00000479638
ENST00000611276 ENSP00000482542
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003810 protein-glutamine gamma-glutamyltransferase activity
GO:0046872 metal ion binding
Biological Process
GO:0006464 cellular protein modification process
GO:0008544 epidermis development
GO:0018149 peptide cross-linking
Cellular Component
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_004245 NM_201631
HUGO
OMIM
CCDS CCDS32211 CCDS32212
HPRD
IMGT
EMBL
GenPept
RNA Seq Atlas