CPT2

Description		carnitine palmitoyltransferase 2
Image		No pdb structure
GO Annotations	Cellular Component	Nucleoplasm Nucleolus Mitochondrion Mitochondrial Inner Membrane
	Molecular Function	Carnitine O-palmitoyltransferase Activity
	Biological Process	In Utero Embryonic Development Fatty Acid Beta-oxidation Carnitine Shuttle Regulation Of Lipid Metabolic Process Positive Regulation Of Cold-induced Thermogenesis
Pathways		PPARA activates gene expression Carnitine metabolism
Drugs		L-Carnitine Perhexiline
Diseases		Disorders of fatty-acid oxidation, including: Medium-chain (MC) acyl-CoA dehydrogenase (AD) deficiency (MCADD); Short-chain AD deficiency (SCADD) ; Short-branched-chain AD deficiency (SBCADD) ; Very long-chain AD deficiency (VLCADD) ; Long-chain 3-hydroxyacyl CoA dehydrogenase deficiency (LCHADD) ; Trifunctional protein deficiency (TFP); Carnitine palmitoyltransferase deficiency (CPT); Carnitine-acylcarnitine translocase deficiency (CACT); Systemic primary carnitine deficiency (CDSP)
GWAS		Blood metabolite levels ( 24816252) Feeling hurt ( 29500382) Metabolite levels ( 31628463) Urinary metabolite modules (eigenmetabolites) in chronic kidney disease ( 31959995)
Interacting Genes		1 interacting genes: MTDH
Entrez ID		1376
HPRD ID		02802
Ensembl ID		ENSG00000157184
Uniprot IDs		A0A140VK13 A0A1B0GTB8 P23786
PDB IDs
Enriched GO Terms of Interacting Partners?
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