SLC9B2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 is a protein that in humans is encoded by the SLC9B2 gene.[5]

AliasesSLC9B2, NHA2, NHE10, NHEDC2, solute carrier family 9 member B2
End103,085,829 bp[1]
Quick facts Identifiers, Aliases ...
SLC9B2
Identifiers
AliasesSLC9B2, NHA2, NHE10, NHEDC2, solute carrier family 9 member B2
External IDsOMIM: 611789; MGI: 2140077; HomoloGene: 45381; GeneCards: SLC9B2; OMA:SLC9B2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001300754
NM_001300756
NM_178833

NM_178877

RefSeq (protein)

NP_849208

Location (UCSC)Chr 4: 103.02 – 103.09 MbChr 3: 135.01 – 135.05 Mb
PubMed search[3][4]
Wikidata
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Function

Sodium–hydrogen antiporters, such as NHEDC2, convert the proton motive force established by the respiratory chain or the F1F0 mitochondrial ATPase into sodium gradients that drive other energy-requiring processes, transduce environmental signals into cell responses, or function in drug efflux.[6]

References

Further reading

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