CKMT1B creatine kinase, mitochondrial 1B [ Homo sapiens (human) ]
Source: NCBI Gene (ID 1159)
Symbol: CKMT1B
Full name: creatine kinase, mitochondrial 1B
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: CKMT; CKMT1; UMTCK
Summary: Mitochondrial creatine (MtCK) kinase is responsible for the transfer of high energy phosphate from mitochondria to the cytosolic carrier, creatine. It belongs to the creatine kinase isoenzyme family. It exists as two isoenzymes, sarcomeric MtCK and ubiquitous MtCK, encoded by separate genes. Mitochondrial creatine kinase occurs in two different oligomeric forms: dimers and octamers, in contrast to the exclusively dimeric cytosolic creatine kinase isoenzymes. Many malignant cancers with poor prognosis have shown overexpression of ubiquitous mitochondrial creatine kinase; this may be related to high energy turnover and failure to eliminate cancer cells via apoptosis. Ubiquitous mitochondrial creatine kinase has 80% homology with the coding exons of sarcomeric mitochondrial creatine kinase. Two genes located near each other on chromosome 15 have been identified which encode identical mitochondrial creatine kinase proteins. [provided by RefSeq, Jul 2008]
Expression: Biased expression in colon (RPKM 40.9), duodenum (RPKM 39.5) and 13 other tissues
Orthologs: mouse
Gene size: 6550bp
Exon count: 10