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MGP006958

Record overview

MGPD IDMGP006958
Gene ID285195
SpeciesHomo sapiens (Human)
Gene Namesolute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9
Gene Symbol SLC9A9
SynonymsNHE9; AUTS16;
Alternate namessodium/hydrogen exchanger 9; Na(+)/H(+) exchanger 9; putative protein product of Nbla00118; sodium/proton exchanger NHE9; solute carrier family 9 (sodium/hydrogen exchanger), isoform 9;
Chromosome3
Map Location3q24
SummaryThis gene encodes a sodium/proton exchanger that is a member of the solute carrier 9 protein family. The encoded protein localizes the to the late recycling endosomes and may play an important role in maintaining cation homeostasis. Mutations in this gene are associated with autism susceptibility 16 and attention-deficit/hyperactivity disorder. [provided by RefSeq, Mar 2012]
OrthologsView orthologs and multiple alignments for SLC9A9

Proteins

sodium/hydrogen exchanger 9
Refseq ID:NP_775924
Protein GI:27734935
UniProt ID:Q8IVB4
mRNA ID:NM_173653
Length:645
RefSeq Status:
MERQSRVMSEKDEYQFQHQGAVELLVFNFLLILTILTIWLFKNHRFRFLHETGGAMVYGLIMGLILRYATAPTDIESGTVYDCVKLTFSPSTLLVNITDQ
VYEYKYKREISQHNINPHQGNAILEKMTFDPEIFFNVLLPPIIFHAGYSLKKRHFFQNLGSILTYAFLGTAISCIVIGLIMYGFVKAMIHAGQLKNGDFH
FTDCLFFGSLMSATDPVTVLAIFHELHVDPDLYTLLFGESVLNDAVAIVLTYSISIYSPKENPNAFDAAAFFQSVGNFLGIFAGSFAMGSAYAIITALLT
KFTKLCEFPMLETGLFFLLSWSAFLSAEAAGLTGIVAVLFCGVTQAHYTYNNLSSDSKIRTKQLFEFMNFLAENVIFCYMGLALFTFQNHIFNALFILGA
FLAIFVARACNIYPLSFLLNLGRKQKIPWNFQHMMMFSGLRGAIAFALAIRNTESQPKQMMFTTTLLLVFFTVWVFGGGTTPMLTWLQIRVGVDLDENLK
EDPSSQHQEANNLDKNMTKAESARLFRMWYSFDHKYLKPILTHSGPPLTTTLPEWCGPISRLLTSPQAYGEQLKEDDVECIVNQDELAINYQEQASSPCS
PPARLGLDQKASPQTPGKENIYEGDLGLGGYELKLEQTLGQSQLN
 
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