JPT2 and SLC25A20

Data Source:
HPRD (two hybrid)

		JPT2	SLC25A20
Description		Jupiter microtubule associated homolog 2	solute carrier family 25 member 20
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleus Cytosol Plasma Membrane	Mitochondrion Mitochondrial Inner Membrane Cytosol Integral Component Of 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		8 interacting genes: CDC42 CNTFR CSNK1D EGR2 RASA4 SEPTIN2 SLC25A20 XRCC6	1 interacting genes: JPT2
Entrez ID		90861	788
HPRD ID		12674	01953
Ensembl ID		ENSG00000206053	ENSG00000178537
Uniprot IDs		Q9H910	O43772
PDB IDs
Enriched GO Terms of Interacting Partners?
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