SLC25A20

Description		solute carrier family 25 member 20
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Envelope Mitochondrial Inner Membrane Cytosol Membrane
	Molecular Function	Carnitine:O-acyl-L-carnitine Antiporter Activity Protein Binding O-acyl-L-carnitine Transmembrane Transporter Activity
	Biological Process	In Utero Embryonic Development Mitochondrial Transport Carnitine Shuttle Lipid Transport Carnitine Transmembrane Transport O-acyl-L-carnitine Transmembrane Transport
Pathways		Carnitine shuttle
Drugs		Levocarnitine
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 (MOSTest) ( 32665545) Crohn's disease ( 28067908) Eosinophil percentage of white cells ( 32888494) Immature fraction of reticulocytes ( 32888494) Inflammatory bowel disease ( 28067908) Metabolite levels ( 23823483) Reticulocyte count ( 32888494) Reticulocyte fraction of red cells ( 32888494) Subcortical volume (min-P) ( 32665545) Subcortical volume (MOSTest) ( 32665545) Ulcerative colitis ( 28067908)
Interacting Genes		1 interacting genes: JPT2
Entrez ID		788
HPRD ID		01953
Ensembl ID		ENSG00000178537
Uniprot IDs		O43772
PDB IDs
Enriched GO Terms of Interacting Partners?		Endocytosis Involved In Viral Entry Into Host Cell Symbiont Entry Into Host Cell Regulation Of Calcium-mediated Signaling Biological Process Involved In Interaction With Host
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