SLC37A3 - solute carrier family 37 member 3 Gene

Homo sapiens

Also known as SPX3

Gene ID: 84255 | Gene type: protein coding

About SLC37A3

Cytogenetic location: 7q34 Genomic coordinates (GRCh38): 7:140,333,752-140,398,530 (from NCBI)

This gene has 28 transcripts (splice variants), 295 orthologues and 12 paralogues. Ubiquitous expression in endometrium (RPKM 19.0), thyroid (RPKM 9.8) and 25 other tissues.

Summary

Predicted to enable transmembrane transporter activity. Predicted to be involved in carbohydrate transport and transmembrane transport. Is integral component of endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC37A3 Products(9)

mRNA	Protein	Name
NM_001287498.2	NP_001274427.1	sugar phosphate exchanger 3 isoform 3
NM_001363373.1	NP_001350302.1	sugar phosphate exchanger 3 isoform 4
NM_001363374.1	NP_001350303.1	sugar phosphate exchanger 3 isoform 5
NM_001363375.1	NP_001350304.1	sugar phosphate exchanger 3 isoform 6
NM_001363376.1	NP_001350305.1	sugar phosphate exchanger 3 isoform 7
NM_001363377.1	NP_001350306.1	sugar phosphate exchanger 3 isoform 8
NM_001363378.1	NP_001350307.1	sugar phosphate exchanger 3 isoform 9
NM_032295.4	NP_115671.1	sugar phosphate exchanger 3 isoform 2
NM_207113.3	NP_996996.1	sugar phosphate exchanger 3 isoform 1

SLC37A3 Protein Structure

MFS_1

0
100
200
300
400
494 a.a.

Protein Preferred Names

Protein Names

sugar phosphate exchanger 3

solute carrier family 37 (glycerol-3-phosphate transporter), member 3

Related Diseases

Diseases

Alias

Deafness, Autosomal Recessive 8

Neurosensory Nonsyndromic Recessive Deafness 8	DFNB8
Dfnb10	Deafness, Autosomal Recessive 10
Deafness, Childhood-Onset Neurosensory, Autosomal Recessive 8	Nsrd8
Autosomal Recessive Nonsyndromic Deafness 8	Deafness, Autosomal Recessive 8/10
Autosomal Recessive Deafness 10	Autosomal Recessive Deafness 8
Childhood-Onset Neurosensory Autosomal Recessive Deafness 8	Nrsd8
Deafness, Autosomal Recessive, 8	Childhood-Onset Neurosensory Deafness Autosomal Recessive 8
Deafness Autosomal Recessive 10	Deafness Autosomal Recessive 8/10
Deafness Neurosensory Autosomal Recessive 8	Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 8
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 8	Deafness, Autosomal Recessive, Type 8/10

Caffey Disease

Infantile Cortical Hyperostosis	CAFYD
Cortical Congenital Hyperostosis	Caffey-Silverman Syndrome
De Toni-Caffey Disease	Hyperostosis Cortical Infantile
Hyperostosis, Cortical, Congenital

Glycerol Kinase Deficiency

Hyperglycerolemia	GKD
Gk Deficiency	Gk1 Deficiency
Deficiency Of Glycerol Kinase	Isolated Glycerol Kinase Deficiency
Glycerol Kinase Deficiency, Adult Form	Glycerol Kinase Deficiency, Juvenile Form
Deficiency, Glycerol Kinase

Glycogen Storage Disease Ia

Von Gierke Disease	Glycogen Storage Disease Type I
Glycogen Storage Disease I	Hepatorenal Form Of Glycogen Storage Disease
Hepatorenal Glycogenosis	Glucose-6-Phosphatase Deficiency
Glycogen Storage Disease, Type I	Glycogen Storage Disease Due To Glucose-6-Phosphatase Deficiency Type Ia
GSD1A	Gsd1
Von Gierke'S Disease	Glycogen Storage Disease Type 1a
Glycogen Storage Disease 1a	Glucose-6-Phosphate Transport Defect
Gsd Ia	Deficiency Of Glucose-6-Phosphatase
Glycogenosis Type I	Glucose-6-Phosphatase Deficiency Glycogen Storage Disease
Glycogenosis Type 1	Glucose-6-Phosphate Deficiency
Gsd I	Gsd Type I
G6p Deficiency Type 1a	Gsd Due To G6p Deficiency Type 1a
Gsd Due To G6p Deficiency Type Ia	Gsd Type 1a
Gsdia	Glycogen Storage Disease Due To G6p Deficiency Type Ia
Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type 1a	Glycogenosis Due To Glucose-6-Phosphatase Deficiency Type Ia
Glycogenosis Type Ia	Gsd-Ia
Storage Disease, Glycogen, Type 1a	Glycogen Storage Disease Type Ia

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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13215	SLC37A3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLC37A3	RGD	RGD:1310346
Canis familiaris	SLC37A3	VGNC	VGNC:46388
Mus musculus	SLC37A3	MGD	MGI:1919394
Felis catus	SLC37A3	VGNC	VGNC:80719
Bos taurus	SLC37A3	VGNC	VGNC:34844
Macaca mulatta	SLC37A3	VGNC	VGNC:81574

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