SLC13A4 - solute carrier family 13 member 4 Gene

Homo sapiens

Also known as NAS2; SUT1; SUT-1

Gene ID: 26266 | Gene type: protein coding

About SLC13A4

Cytogenetic location: 7q33 Genomic coordinates (GRCh38): 7:135,681,231-135,728,186 (from NCBI)

This gene has 8 transcripts (splice variants), 214 orthologues and 5 paralogues. Biased expression in placenta (RPKM 28.4) and testis (RPKM 3.0).

Summary

Predicted to enable sodium:sulfate symporter activity. Predicted to be involved in anion transmembrane transport. Predicted to be located in plasma membrane. Predicted to be integral component of plasma membrane. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC13A4 Products(2)

mRNA	Protein	Name
NM_001318192.2	NP_001305121.1	solute carrier family 13 member 4 isoform 1
NM_012450.4	NP_036582.2	solute carrier family 13 member 4 isoform 2

SLC13A4 Protein Structure

Na_sulph_symp

0
100
200
300
400
500
626 a.a.

Protein Preferred Names

Protein Names

solute carrier family 13 member 4

Na(+)/sulfate cotransporter SUT-1

Related Diseases

Diseases

Alias

Chondrodysplasia With Joint Dislocations, Gpapp Type

Gpapp Deficiency	Chondrodysplasia With Joint Dislocations Gpapp Type
CDP-GPAPP	Chondrodysplasia, With Joint Dislocations, Gpapp Type

Developmental And Epileptic Encephalopathy 25

Developmental And Epileptic Encephalopathy, 25	Dee25
Developmental And Epileptic Encephalopathy 25, With Amelogenesis Imperfecta	Early Infantile Epileptic Encephalopathy 25
Encephalopathy, Epileptic, Early Infantile, Type 25

Myopathy, Myosin Storage, Autosomal Dominant

MSMA	Myopathy, Hyaline Body, Autosomal Dominant
Myopathy With Lysis Of Type I Myofibrils	Autosomal Dominant Hyaline Body Myopathy
Hyaline Body Myopathy Autosomal Dominant

Achondrogenesis, Type Ib

ACG1B	Achondrogenesis Type Ib
Achondrogenesis Type 1b	Achondrogenesis Ib
Achondrogenesis Fraccaro Type	Achondrogenesis, Fraccaro Type
Achondrogenesis, Parenti-Fraccaro Type	Achondrogenesis 1b
Acg-Ib	Fraccaro Achondrogenesis

Schizophrenia 2

SCZD2	Schizophrenia Susceptibility Locus, Chromosome 11q-Related
Schizophrenia Susceptibility Locus Chromosome 11q-Related

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-RS13008	SLC13A4 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	SLC13A4	MGD	MGI:2442367
Macaca mulatta	SLC13A4	VGNC	VGNC:77489
Felis catus	SLC13A4	VGNC	VGNC:102703
Canis familiaris	SLC13A4	VGNC	VGNC:46230
Bos taurus	SLC13A4	VGNC	VGNC:34676
Rattus norvegicus	SLC13A4	RGD	RGD:1359715

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