CKMT1B - creatine kinase, mitochondrial 1B Gene

Homo sapiens

Also known as CKMT; CKMT1; UMTCK

Gene ID: 1159 | Gene type: protein coding

About CKMT1B

Cytogenetic location: 15q15.3 Genomic coordinates (GRCh38): 15:43,592,857-43,599,406 (from NCBI)

This gene has 15 transcripts (splice variants), 217 orthologues and 4 paralogues. Biased expression in colon (RPKM 40.9), duodenum (RPKM 39.5) and 13 other tissues.

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]

CKMT1B Products(2)

mRNA	Protein	Name
NM_001375484.1	NP_001362413.1	creatine kinase U-type, mitochondrial precursor
NM_020990.5	NP_066270.1	creatine kinase U-type, mitochondrial precursor

CKMT1B Protein Structure

ATP-gua_PtransN

ATP-gua_Ptrans

0
100
200
300
417 a.a.

Protein Preferred Names

Protein Names

creatine kinase U-type, mitochondrial

U-MtCK

Recombinant CKMT1B Proteins

Cat. No.	Product Name	Accession	Purity
HY-P76264	CKMT1A Protein, Human (sf9, His)	P12532 (A40-H417)	≥95%

Related Diseases

Diseases

Alias

Mitochondrial Complex V Deficiency, Nuclear Type 3

Mitochondrial Complex Iii Deficiency Nuclear Type 5	MC5DN3
Mitochondrial Complex Iii Deficiency, Nuclear Type 5	Mitochondrial Complex V Deficiency Nuclear Type 3
MC3DN5	Mitochondrial Complex V Deficiency, Atp5e Type
Mitochondrial Complex Iii Deficiency, Nuclear 5	Mitochondrial Complex V Deficiency, Nuclear Type 3
Mitochondrial Complex V Deficiency Atp5e Type	Mitochondrial Complex V Deficiency Type 3
Mitochondrial Complex V Deficiency, Nuclear, Type 3

Cardiomyopathy, Dilated, 1ee

Dilated Cardiomyopathy 1ee	CMD1EE
Cardiomyopathy, Dilated 1ee	Cardiomyopathy, Dilated, Type 1ee

Cerebral Creatine Deficiency Syndrome

Deficiency, Cerebral Creatine, Syndrome

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02740	CKMT1B Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	CKMT1B	MGD	MGI:99441
Rattus norvegicus	CKMT1B	RGD	RGD:61976

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