1. Gene
  2. SLC8A2 - solute carrier family 8 member A2 Gene

SLC8A2 - solute carrier family 8 member A2 Gene

Homo sapiens

Also known as NCX2

Gene ID: 6543 | Gene type: protein coding

About SLC8A2

Cytogenetic location: 19q13.32 Genomic coordinates (GRCh38): 19:47,428,017-47,471,893 (from NCBI)

This gene has 7 transcripts (splice variants), 200 orthologues and 7 paralogues. Biased expression in brain (RPKM 19.6), endometrium (RPKM 1.5) and 1 other tissue.

Summary

Predicted to enable calcium:cation antiporter activity involved in regulation of postsynaptic cytosolic calcium ion concentration and calcium:sodium antiporter activity. Predicted to be involved in several processes, including inorganic cation transmembrane transport; learning or memory; and regulation of short-term neuronal synaptic plasticity. Predicted to act upstream of or within several processes, including modulation of chemical synaptic transmission; regulation of action potential firing pattern; and response to ischemia. Part of presynapse. Biomarker of Alzheimer's disease. [provided by Alliance of Genome Resources, Apr 2022]

SLC8A2 Products(1)

mRNA Protein Name
NM_015063.3 NP_055878.1 sodium/calcium exchanger 2 precursor

SLC8A2 Protein Structure

Na_Ca_ex

Na_Ca_ex: Sodium/calcium exchanger protein (84 - 243)

Calx-beta

Calx-beta: Calx-beta domain (389 - 482)

Calx-beta

Calx-beta: Calx-beta domain (512 - 611)

Na_Ca_ex

Na_Ca_ex: Sodium/calcium exchanger protein (758 - 909)

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  • 921 a.a.
Protein Preferred Names Protein Names

sodium/calcium exchanger 2

Na(+)/Ca(2+)-exchange protein 2

Related Diseases

Diseases Alias
Ischemia

Acute Coronary Syndrome

Schnyder Corneal Dystrophy

Schnyder Crystalline Corneal Dystrophy

SCCD

Corneal Dystrophy, Crystalline, Of Schnyder

Corneal Dystrophy, Schnyder Type

Corneal Dystrophy Crystalline Of Schnyder

Crystalline Stromal Dystrophy

Hereditary Crystalline Stromal Dystrophy Of Schnyder

Scd

Corneal Dystrophy, Schnyder

Schnyder Crystalline Dystrophy Sine Crystals

Dystrophy, Corneal, Crystalline, Schnyder

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus SLC8A2 MGD MGI:107996
Canis familiaris SLC8A2 VGNC VGNC:46481
Rattus norvegicus SLC8A2 RGD RGD:620194
Bos taurus SLC8A2 VGNC VGNC:34936
Felis catus SLC8A2 VGNC VGNC:65429
Macaca mulatta SLC8A2 VGNC VGNC:77635