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Protein Coding Gene : Ckmt2 creatine kinase, mitochondrial 2
Primary Identifier  MGI:1923972 Organism  mouse, laboratory
Chromosome  13 NCBI Gene Number  76722
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable cardiolipin binding activity and creatine kinase activity. Predicted to be involved in phosphocreatine biosynthetic process. Predicted to act upstream of or within phosphocreatine metabolic process. Located in mitochondrion. Is expressed in several structures, including gut; heart; lung; skeletal muscle; and thymus. Orthologous to human CKMT2 (creatine kinase, mitochondrial 2).
PHENOTYPE: The hearts of mice homozygous for disruptions of this gene have hypertrophic and dilated left ventricles exhibit functional abnormalities. [provided by MGI curators]
  • synonyms:
  • RIKEN cDNA 2300008A19 gene,
  • Ckmt2,
  • ScCKmit,
  • creatine kinase, mitochondrial 2,
  • 2300008A19Rik
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Features --> Cross References

Genome

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0 Exons

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1 Involved In Mutations

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

3 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

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