SLC37A4 (solute carrier family 37 member 4)

2007-06-01  

Identity

HGNC
LOCATION
11q23.3
LOCUSID
ALIAS
G6PT1,G6PT2,G6PT3,GSD1b,GSD1c,GSD1d,PRO0685,TRG-19,TRG19

Other Information

Locus ID:

NCBI: 2542
MIM: 602671
HGNC: 4061
Ensembl: ENSG00000137700

Variants:

dbSNP: 2542
ClinVar: 2542
TCGA: ENSG00000137700
COSMIC: SLC37A4

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000137700ENST00000330775U3KPU7
ENSG00000137700ENST00000357590U3KQS2
ENSG00000137700ENST00000538950U3KQL4
ENSG00000137700ENST00000545985U3KPU7

Expression (GTEx)

0
10
20
30
40
50
60
70
80

Pathways

PathwaySourceExternal ID
Carbohydrate digestion and absorptionKEGGko04973
Carbohydrate digestion and absorptionKEGGhsa04973
Transmembrane transport of small moleculesREACTOMER-HSA-382551
SLC-mediated transmembrane transportREACTOMER-HSA-425407
Hexose transportREACTOMER-HSA-189200
Glucose transportREACTOMER-HSA-70153
MetabolismREACTOMER-HSA-1430728
Metabolism of carbohydratesREACTOMER-HSA-71387

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
380875032023Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review.1
380875032023Three novel SLC37A4 variants in glycogen storage disease type 1b and a literature review.1
332802762021A novel SLC37A4 missense mutation in GSD-Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosis.1
339642072021A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.7
332802762021A novel SLC37A4 missense mutation in GSD-Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosis.1
339642072021A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction.7
320052212020Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b).2
320052212020Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b).2
309518562019CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.3
309518562019CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.3
286858442018Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.12
292389662018Aberrant proliferation and differentiation of glycogen storage disease type Ib mesenchymal stem cells.3
286858442018Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.12
292389662018Aberrant proliferation and differentiation of glycogen storage disease type Ib mesenchymal stem cells.3
282247732017Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease Ib.12

Citation

Dessen P

SLC37A4 (solute carrier family 37 member 4)

Atlas Genet Cytogenet Oncol Haematol. 2007-06-01

Online version: http://atlasgeneticsoncology.org/gene/47556/slc37a4