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GeneQ14903608· pop 13· linked from 334 articles

Also known as G-ALPHA-h, GNAH, HEL-S-45, TG2, TGC, TG(C), transglutaminase 2, G(h)

protein-coding gene in the species Homo sapiens

Gene data

TGM2
Name
transglutaminase 2
Type
protein-coding
Position
38,127,385–38,168,463 (−)
Aliases
G(h), TG(C), TGC, hTG2, tTG
RefSeq RNA
NM_001323316.2, NM_001323317.2, NM_001323318.2, NM_004613.4, NM_198951.3
RefSeq protein
NP_001310245.1, NP_001310246.1, NP_001310247.1, NP_004604.2, NP_945189.1

Transglutaminases are enzymes that catalyze the crosslinking of proteins by epsilon-gamma glutamyl lysine isopeptide bonds. While the primary structure of transglutaminases is not conserved, they all have the same amino acid sequence at their active sites and their activity is calcium-dependent. The protein encoded by this gene acts as a monomer, is induced by retinoic acid, and appears to be involved in apoptosis. Finally, the encoded protein is the autoantigen implicated in celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

transglutaminase 2

Symbol
TGM2
Biotype
Protein coding
Organism
Homo sapiens
Location
20:38,127,385-38,168,463
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI