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Gene : CKM Homo sapiens

Name  ? creatine kinase, M-type Cytological Location  19q13.32
Brief Description  creatine kinase, M-type
Description  The protein encoded by this gene is a cytoplasmic enzyme involved in energy homeostasis and is an important serum marker for myocardial infarction. The encoded protein reversibly catalyzes the transfer of phosphate between ATP and various phosphogens such as creatine phosphate. It acts as a homodimer in striated muscle as well as in other tissues, and as a heterodimer with a similar brain isozyme in heart. The encoded protein is a member of the ATP:guanido phosphotransferase protein family. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000181782,
  • NM_001824,
  • HGNC:1994,
  • M-CK,
  • CKMM,
  • CKMM,
  • CPK-M,
  • CKM,
  • M14780,
  • uc002pbd.5,
  • creatine kinase, muscle
  • identifiers:
  • 1158,
  • ENSG00000104879,
  • CKM

Genome feature

Region: gene ? Length: 16463  
Location: 19:45306413-45322875 reverse strand Cyto location: 19q13.32

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

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29 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results