SLC38A2 - solute carrier family 38 member 2 Gene

Homo sapiens

Also known as ATA2; SAT2; SNAT2; PRO1068

Gene ID: 54407 | Gene type: protein coding

About SLC38A2

Cytogenetic location: 12q13.11 Genomic coordinates (GRCh38): 12:46,358,188-46,372,773 (from NCBI)

This gene has 14 transcripts (splice variants), 260 orthologues and 15 paralogues. Ubiquitous expression in skin (RPKM 105.3), liver (RPKM 101.3) and 25 other tissues.

Summary

Enables neutral amino acid:sodium symporter activity. Involved in several processes, including amino acid transport; cellular response to arsenite(3-); and positive regulation of RNA splicing. Located in cytoplasm and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC38A2 Products(2)

mRNA	Protein	Name
NM_001307936.2	NP_001294865.1	sodium-coupled neutral amino acid symporter 2 isoform 2 precursor
NM_018976.5	NP_061849.2	sodium-coupled neutral amino acid symporter 2 isoform 1

SLC38A2 Protein Structure

Aa_trans

0
100
200
300
400
506 a.a.

Protein Preferred Names

Protein Names

sodium-coupled neutral amino acid symporter 2

sodium-coupled neutral amino acid transporter 2

amino acid transporter 2

Related Diseases

Diseases

Alias

Adult Syndrome

Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome	Acro Dermato Ungual Lacrimal Tooth Syndrome
Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome	Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome
Adult

Hartnup Disorder

Hartnup Disease	HND
Neutral 1 Amino Acid Transport Defect	Neutral Amino Acid Transport Defect
Deficiency Of Tryptophan Oxygenase	Hartnup'S Disease
Aminoaciduria, Hartnup Type	Disorder Of Neutral Amino Acid Transport

Persistent Fetal Circulation Syndrome

Persistent Fetal Circulation	Fetal Circulation
Persistent Pulmonary Hypertension Of The Newborn	Congenital Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
Persistent Foetal Circulation	Persistent Foetal Circulation Syndrome
Pfc - [Persistent Fetal Circulation] Syndrome	Pphn - [Persistent Pulmonary Hypertension Of The Newborn]
Newborn Pulmonary Hypertension	Primary Pulmonary Hypertension Of Newborn

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-RS13220	SLC38A2 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLC38A2	RGD	RGD:69420
Bos taurus	SLC38A2	VGNC	VGNC:34849
Canis familiaris	SLC38A2	VGNC	VGNC:46393
Felis catus	SLC38A2	VGNC	VGNC:65345
Macaca mulatta	SLC38A2	VGNC	VGNC:77469
Mus musculus	SLC38A2	MGD	MGI:1915010

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