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Gene : CPT2 Homo sapiens

Name  ? carnitine palmitoyltransferase 2 Cytological Location  1p32.3
Brief Description  carnitine palmitoyltransferase 2
Description  The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]
  • synonyms:
  • BC002445,
  • OTTHUMG00000008942,
  • CPT1,
  • CPT1,
  • HGNC:2330,
  • CPT2,
  • carnitine palmitoyltransferase II,
  • IIAE4,
  • NM_000098,
  • uc001cvb.4
  • identifiers:
  • 1376,
  • ENSG00000157184,
  • CPT2

Genome feature

Region: gene ? Length: 17374  
Location: 1:53196824-53214197 Cyto location: 1p32.3

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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4 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



226 SN Ps

5 Cross References

19 Data Sets

11 Homologues

0 Located Features

97 Rna Seq Results