EMG1 and SLC25A38

		EMG1	SLC25A38
Description		EMG1 N1-specific pseudouridine methyltransferase	solute carrier family 25 member 38
Image			No pdb structure
GO Annotations	Cellular Component	Nucleus Nucleoplasm Chromosome Nucleolus Cytoplasm Small-subunit Processome	Mitochondrion Mitochondrial Inner Membrane Integral Component Of Membrane
	Molecular Function	RNA Binding Protein Binding RRNA Binding Identical Protein Binding RRNA (pseudouridine) Methyltransferase Activity	Glycine Transmembrane Transporter Activity
	Biological Process	Blastocyst Development RRNA Processing Nucleologenesis Ribosomal Small Subunit Biogenesis RRNA Base Methylation	Heme Biosynthetic Process Erythrocyte Differentiation Glycine Import Into Mitochondrion
Pathways		rRNA modification in the nucleus and cytosol Major pathway of rRNA processing in the nucleolus and cytosol
Drugs
Diseases		Bowen-Conradi syndrome (BCS)	Sideroblastic anemia, including: Pyridoxine-refractory autosomal recessive sideroblastic anemia (PRARSA); X-linked sideroblastic anemia (XLSA); X-linked sideroblastic anemia with ataxia (ASAT)
GWAS
Interacting Genes		15 interacting genes: ANXA3 APP CTSE FAM74A4 HIVEP1 HSD3B7 IL7R KHDRBS1 MCPH1 NAA80 PSMB7 PSME1 SLC25A38 SUMO2 ZNF768	3 interacting genes: EMG1 NOL12 ZSCAN16
Entrez ID		10436	54977
HPRD ID		12803	07925
Ensembl ID		ENSG00000126749	ENSG00000144659
Uniprot IDs		Q92979	A1LP07 Q96DW6
PDB IDs		5FAI
Enriched GO Terms of Interacting Partners?
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