ATP6AP2

Description		ATPase H+ transporting accessory protein 2
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GO Annotations	Cellular Component	Autophagosome Membrane Lysosome Lysosomal Membrane Endoplasmic Reticulum Membrane Plasma Membrane External Side Of Plasma Membrane Integral Component Of Membrane Apical Plasma Membrane Vacuolar Proton-transporting V-type ATPase Complex Cell Junction Axon Dendritic Spine Membrane Cell Body Postsynaptic Membrane Extracellular Exosome Tertiary Granule Membrane Ficolin-1-rich Granule Membrane
	Molecular Function	Protein Binding Signaling Receptor Activity
	Biological Process	Angiotensin Maturation Rostrocaudal Neural Tube Patterning Positive Regulation Of Wnt Signaling Pathway Positive Regulation Of Transforming Growth Factor Beta1 Production Neutrophil Degranulation Regulation Of MAPK Cascade Eye Pigmentation Head Morphogenesis
Pathways		Metabolism of Angiotensinogen to Angiotensins Neutrophil degranulation
Drugs
Diseases		Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
GWAS		Metabolite levels ( 23823483)
Interacting Genes		6 interacting genes: AGT CREB3 GLP1R REN VKORC1 ZBTB16
Entrez ID		10159
HPRD ID		06454
Ensembl ID		ENSG00000182220
Uniprot IDs		O75787
PDB IDs		3LBS 3LC8
Enriched GO Terms of Interacting Partners?
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