QuickView for TGMX (gene)

Gene Symbol:

TGM5 Homo sapiens

Full name:

transglutaminase 5

Synonyms:

PSS2, TGASE5, TGASEX, TGM6, TGMX, TGX, protein-glutamine gamma-glutamyltransferase 5, TG(X), TGase X, TGase-5, transglutaminase V, transglutaminase X

Genomic Location:

Chr 15: 41312667-41346347

Description:

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

YATTNATC_UNKNOWN ,  GCCATNTTG_YY1_Q6 ,  AR_Q6 ,  YY1_Q6 ,  TGCCAAR_NF1_Q6 ,  MYB_Q6 ,  RTTTNNNYTGGM_UNKNOWN ,  T3R_Q6

Cytogenetic Map:

15q15.2

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