SLC9B2 information

SLC9B2
Identifiers
Aliases	SLC9B2, NHA2, NHE10, NHEDC2, solute carrier family 9 member B2
External IDs	OMIM: 611789; MGI: 2140077; HomoloGene: 45381; GeneCards: SLC9B2; OMA:SLC9B2 - orthologs
Gene location (Human)
Chr.	Chromosome 4 (human)
End	103,085,829 bp
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)
End	135,051,148 bp
RNA expression pattern
	Top expressed in
	sural nerve; ; prefrontal cortex; ; Achilles tendon; ; tibia; ; Brodmann area 9; ; cerebellar hemisphere; ; right frontal lobe; ; liver; ; right hemisphere of cerebellum; ; islet of Langerhans;
	Top expressed in
	body of femur; ; membranous bone; ; Dermatocranium; ; mandible; ; maxilla; ; upper lip; ; embryo; ; embryo; ; epithelium of stomach; ; tibiofemoral joint;
	More reference expression data
	n/a
Gene ontology
Molecular function	solute:proton antiporter activity; antiporter activity; monovalent cation:proton antiporter activity; lithium:proton antiporter activity; sodium:proton antiporter activity; identical protein binding;
Cellular component	integral component of membrane; membrane; mitochondrion; mitochondrial inner membrane; endosome membrane; basolateral plasma membrane; synaptic vesicle membrane; sperm principal piece; plasma membrane; mitochondrial membranes; intracellular vesicle; endosome; apical plasma membrane; cell junction; cytoplasmic vesicle; cell projection; synapse; cilium; motile cilium;
Biological process	proton transmembrane transport; ion transmembrane transport; cation transport; ion transport; positive regulation of osteoclast development; transmembrane transport; flagellated sperm motility; sodium ion transmembrane transport; regulation of insulin secretion involved in cellular response to glucose stimulus; clathrin-dependent endocytosis; sodium ion transport;
	Sources:Amigo / QuickGO
Orthologs
	133308
	97086
	ENSG00000164038
	ENSMUSG00000037994
	Q86UD5
	Q5BKR2
	NM_001300754; NM_001300756; NM_178833
	NM_178877
NP_001287683; NP_001287685; NP_849155; NP_001357128; NP_001357129;
	NP_001357130; NP_001357131; NP_001357132; NP_001357133; NP_001357134; NP_001357135; NP_001357136
	NP_849208
	Wikidata
View/Edit Human	View/Edit Mouse

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]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000164038 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000037994 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: Solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2".

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000164038 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000037994 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: Solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2".