SLC25A20 and JPT2

Data Source:
HPRD (two hybrid)

		SLC25A20	JPT2
Description		solute carrier family 25 member 20	Jupiter microtubule associated homolog 2
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Cytosol Integral Component Of Membrane	Nucleus Cytosol Plasma Membrane
	Molecular Function	Protein Binding Acyl Carnitine Transmembrane Transporter Activity
	Biological Process	In Utero Embryonic Development Carnitine Shuttle Carnitine Transmembrane Transport Acyl Carnitine Transmembrane Transport
Pathways		Carnitine metabolism
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		Blood protein levels ( 28240269) 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	8 interacting genes: CDC42 CNTFR CSNK1D EGR2 RASA4 SEPTIN2 SLC25A20 XRCC6
Entrez ID		788	90861
HPRD ID		01953	12674
Ensembl ID		ENSG00000178537	ENSG00000206053
Uniprot IDs		O43772	Q9H910
PDB IDs
Enriched GO Terms of Interacting Partners?
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