CPT2

Description		carnitine palmitoyltransferase 2
Image		No pdb structure
GO Annotations	Cellular Component	Nucleoplasm Nucleolus Mitochondrion Mitochondrial Inner Membrane Mitochondrial Matrix Membrane
	Molecular Function	Carnitine O-palmitoyltransferase Activity Protein Binding Carnitine O-octanoyltransferase Activity Transferase Activity Acyltransferase Activity
	Biological Process	Long-chain Fatty Acid Metabolic Process In Utero Embryonic Development Lipid Metabolic Process Fatty Acid Metabolic Process Fatty Acid Beta-oxidation Carnitine Shuttle Carnitine Metabolic Process Positive Regulation Of Cold-induced Thermogenesis
Pathways		PPARA activates gene expression Carnitine shuttle
Drugs		Levocarnitine 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		Brain morphology (min-P) ( 32665545) Brain morphology (MOSTest) ( 32665545) Cortical surface area (min-P) ( 32665545) Cortical surface area (MOSTest) ( 32665545) Cortical thickness (min-P) ( 32665545) Cortical thickness (MOSTest) ( 32665545) Feeling hurt ( 29500382) Metabolite levels ( 31628463) Serum metabolite levels ( 33031748) Subcortical volume (min-P) ( 32665545) Subcortical volume (MOSTest) ( 32665545) 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?		Intercellular Canaliculus
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