ISCA1P1 and NDUFAF2

		ISCA1P1	NDUFAF2
Description		iron-sulfur cluster assembly 1 pseudogene 1	NADH:ubiquinone oxidoreductase complex assembly factor 2
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component		Mitochondrion Mitochondrial Inner Membrane
	Molecular Function		NADH Dehydrogenase (ubiquinone) Activity Electron Transfer Activity
	Biological Process		Respiratory Electron Transport Chain Mitochondrial Respiratory Chain Complex I Assembly Cellular Respiration Negative Regulation Of Insulin Secretion Involved In Cellular Response To Glucose Stimulus Reactive Oxygen Species Metabolic Process
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		Uric acid levels ( 21294900)	Autism spectrum disorder or schizophrenia ( 28540026) Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) ( 31374203) Household income ( 31844048) Household income (MTAG) ( 31844048) Intelligence (MTAG) ( 29326435) Parkinson's disease ( 27182965)
Interacting Genes		1 interacting genes: NDUFAF2	4 interacting genes: C5orf64 GNL3LP1 ISCA1P1 SLC30A5
Entrez ID		389293	91942
HPRD ID		19147	14288
Ensembl ID			ENSG00000164182
Uniprot IDs			A0A0S2Z5U1 Q8N183
PDB IDs
Enriched GO Terms of Interacting Partners?
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