IPO13 and GK

		IPO13	GK
Description		importin 13	glycerol kinase
Image			No pdb structure
GO Annotations	Cellular Component	Nucleus Cytoplasm	Mitochondrion Mitochondrial Outer Membrane Cytosol Extracellular Exosome
	Molecular Function	Protein Binding	Glycerol Kinase Activity Protein Binding ATP Binding Phosphotransferase Activity, Alcohol Group As Acceptor
	Biological Process	Protein Import Into Nucleus	Glycerol Metabolic Process Triglyceride Metabolic Process Phosphorylation Triglyceride Biosynthetic Process Glycerol Catabolic Process Glycerol-3-phosphate Biosynthetic Process
Pathways			Triglyceride biosynthesis
Drugs
Diseases			Glycerol kinase deficiency (GKD), including: Hyperglycerolemia; Chromosome Xp21 deletion syndrome; Adrenal hypoplasia, congenital (AHC); Duchenne muscular dystrophy (DMD)
GWAS		Autism spectrum disorder or schizophrenia ( 28540026)	Cardiovascular risk factors (age interaction) ( 20838585)
Interacting Genes		17 interacting genes: ALX1 CRX EIF1AX GK HMBOX1 MAGOH NPSR1 NUP50 PAX3 PAX6 PBX4 PITX1 PSMA1 RAN RBM8A RPL5 UBE2I	11 interacting genes: AOX1 APCS CLPTM1L CYP3A4 EIF4G1 FBXO28 GPD1 IPO13 NR4A1 OPLAH RXRA
Entrez ID		9670	2710
HPRD ID		13742	08363
Ensembl ID		ENSG00000117408	ENSG00000198814
Uniprot IDs		O94829	B4DH54 P32189
PDB IDs		2X19 2XWU 3ZJY
Enriched GO Terms of Interacting Partners?
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