SLC37A2 - solute carrier family 37 member 2 Gene

Also Known as SPX2; pp11662

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 219855

About SLC37A2

Cytogenetic location: 11q24.2 Genomic coordinates (GRCh38): 11:125,063,305-125,090,516 (from NCBI)

This gene has 6 transcripts (splice variants), 241 orthologues and 12 paralogues. Broad expression in adrenal (RPKM 13.0), salivary gland (RPKM 12.4) and 18 other tissues.

Summary

Enables glucose 6-phosphate:inorganic phosphate antiporter activity. Involved in glucose-6-phosphate transport and phosphate ion transmembrane transport. Is integral component of endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC37A2 Products (2)

mRNA Protein Name
NM_001145290.2 NP_001138762.1 glucose-6-phosphate exchanger SLC37A2 isoform 2
NM_198277.3 NP_938018.1 glucose-6-phosphate exchanger SLC37A2 isoform 1
Molecular Function GO Annotation Evidence Referencias Source
enables glucose 6-phosphate:phosphate antiporter activity EXP
EXP: Inferred from Experiment
21949678 GOA
enables glucose 6-phosphate:phosphate antiporter activity IDA
IDA: Inferred from direct assay
21949678 GOA
Biological Process GO Annotation Evidence Referencias Source
involved in glucose-6-phosphate transport IDA
IDA: Inferred from direct assay
21949678 GOA
involved in phosphate ion transmembrane transport IDA
IDA: Inferred from direct assay
21949678 GOA
Cellular Component GO Annotation Evidence Referencias Source
located in endoplasmic reticulum membrane IDA
IDA: Inferred from direct assay
21949678 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC37A2 Protein Structure

MFS_1

MFS_1: Major Facilitator Superfamily (92 - 414)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 501 a.a.
Protein Preferred Names Protein Names

glucose-6-phosphate exchanger SLC37A2

  • solute carrier family 37 (glucose-6-phosphate transporter), member 2

Related Diseases

Diseases Alias
Caffey Disease
  • Infantile Cortical Hyperostosis

  • CAFYD

  • Cortical Congenital Hyperostosis

  • Caffey-Silverman Syndrome

  • De Toni-Caffey Disease

  • Hyperostosis Cortical Infantile

  • Hyperostosis, Cortical, Congenital

Van Den Ende-Gupta Syndrome
  • VDEGS

  • Blepharophimosis, Arachnodactyly, And Congenital Contractures

  • Marden-Walker-Like Syndrome

  • Marden-Walker-Like Syndrome Without Psychomotor Retardation

  • Marden Walker Like Syndrome

  • Marden-Walker-Like Syndrome Without Psychmotor Retardation

  • Van Den Ende Gupta Syndrome

  • Marden Walker Like Syndrome Without Psychomotor Retardation

  • Blepharophimosis Arachnodactyly And Congenital Contractures

Combined Oxidative Phosphorylation Deficiency 24
  • COXPD24

  • Combined Oxidative Phosphorylation Defect Type 24

  • Oxidative Phosphorylation Deficiency, Combined, Type 24

Combined Oxidative Phosphorylation Deficiency 20
  • COXPD20

  • Combined Oxidative Phosphorylation Defect Type 20

  • Oxidative Phosphorylation Deficiency, Combined, Type 20

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
Bos taurus SLC37A2 VGNC VGNC:34843
Mus musculus SLC37A2 MGD MGI:1929693
Macaca mulatta SLC37A2 VGNC VGNC:107645
Felis catus SLC37A2 VGNC VGNC:81937
Canis familiaris SLC37A2 VGNC VGNC:46387
Rattus norvegicus SLC37A2 RGD RGD:1564160
Others SLC37A2 NCBI