| Name: transglutaminase 2, C polypeptide |
| Aliases:
G[a]h,
tTGas,
TG2,
tissue transglutaminase,
TGase2,
TG C,
tTG,
protein-glutamine gamma-glutamyltransferase
|
| Description: PHENOTYPE: A homozygous null mutation causes alterations in glucose and aerobic energy metabolism, tumor growth, and response to myocardial infarction, liver injury, and LPS-induced sepsis. A second null mutation confers resistance to renal injury, while a third one alters cell adhesion and T cell physiology. [provided by MGI curators] |
| Crossreferences:
MGI:98731,
UniProtKB:G3UXE8,
ENSEMBL:ENSMUSG00000037820,
UniProtKB:P21981,
NCBI_Gene:21817
|
| This information is supplied by the AllianceGenome.org API. |