NDUFAF2

Description		NADH:ubiquinone oxidoreductase complex assembly factor 2
Image		No pdb structure
GO Annotations	Cellular Component	Mitochondrion Mitochondrial Inner Membrane Membrane Respiratory Chain Complex I
	Molecular Function	Protein Binding Protein-containing Complex Binding
	Biological Process	Cell Projection Organization Mitochondrial Respiratory Chain Complex I Assembly Cilium Assembly Negative Regulation Of Insulin Secretion Involved In Cellular Response To Glucose Stimulus
Pathways		Complex I biogenesis
Drugs
Diseases		Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (MT-C1D); Complex II deficiency (MT-C2D); Complex III deficiency (MT-C3D); Complex IV deficiency (MT-C4D); Complex V deficiency (MT-ATPSD); Leigh syndrome (LS); Kearns-Sayre Syndrome (KSS); LCHD deficiency (LCHD); Leber Hereditary Optic Neuropathy (LHON); Myoclonic Epilepsy and Ragged-Red Fiber Disease (MERRF); NARP; MELAS; ACAD9 deficiency; HADH deficiency; HIBCH deficiency; GRACILE syndrome
GWAS		Autism spectrum disorder or schizophrenia ( 28540026) Brain morphology (MOSTest) ( 32665545) Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) ( 31374203) Cortical surface area (MOSTest) ( 32665545) Cortical volume ( 32963231) Household income ( 31844048) Household income (MTAG) ( 31844048) Intelligence (MTAG) ( 29326435) Parkinson's disease ( 27182965) Subcortical volume (MOSTest) ( 32665545)
Novel Interacting Genes		4 novel interacting genes: GNL3LP1 ISCA1P1 LINC03122 SLC30A5
Interacting Genes		9 interacting genes: CYB5B LAT LPAR3 SEC22B SMIM1 SPG21 STX8 TMEM201 TMEM97
Entrez ID		91942
HPRD ID		14288
Ensembl ID		ENSG00000164182
Uniprot IDs		A0A0S2Z5U1 Q8N183
PDB IDs
Enriched GO Terms of Interacting Partners?		Collateral Sprouting
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