SLC9A6

Description		solute carrier family 9 member A6
Image		No pdb structure
GO Annotations	Cellular Component	Cell Mitochondrion Late Endosome Endoplasmic Reticulum Membrane Plasma Membrane Integral Component Of Membrane Dendrite Early Endosome Membrane Intracellular Membrane-bounded Organelle Axon Terminus Axonal Spine Recycling Endosome Recycling Endosome Membrane
	Molecular Function	Sodium:proton Antiporter Activity Potassium:proton Antiporter Activity
	Biological Process	Ion Transport Brain-derived Neurotrophic Factor Receptor Signaling Pathway Axon Extension Neuron Projection Morphogenesis Synapse Organization Regulation Of Neurotrophin TRK Receptor Signaling Pathway Regulation Of Intracellular PH Dendritic Spine Development Potassium Ion Transmembrane Transport Dendrite Extension Anion Transmembrane Transport Sodium Ion Import Across Plasma Membrane Proton Transmembrane Transport
Pathways		Sodium/Proton exchangers Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
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
Interacting Genes		1 interacting genes: CFTR
Entrez ID		10479
HPRD ID		02208
Ensembl ID		ENSG00000198689
Uniprot IDs		A0A1B0GV11 Q92581
PDB IDs
Enriched GO Terms of Interacting Partners?
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