2. Gene
  3. SLC38A9 - solute carrier family 38 member 9 Gene

SLC38A9 - solute carrier family 38 member 9 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as SNAT9; URLC11

Gene ID: 153129 | Gene type: protein coding

About SLC38A9

Cytogenetic location: 5q11.2 Genomic coordinates (GRCh38): 5:55,625,845-55,712,335 (from NCBI)

This gene has 26 transcripts (splice variants), 209 orthologues and 15 paralogues. Broad expression in placenta (RPKM 15.1), testis (RPKM 7.5) and 22 other tissues.

Summary

Enables L-arginine transmembrane transporter activity and L-leucine transmembrane transporter activity. Involved in amino acid transmembrane transport; cellular response to amino acid stimulus; and positive regulation of TOR signaling. Located in late endosome and lysosomal membrane. Is integral component of lysosomal membrane. Colocalizes with Ragulator complex. [provided by Alliance of Genome Resources, Apr 2022]

SLC38A9 Products(8)

mRNA Protein Name
NM_001258286.1 NP_001245215.1 sodium-coupled neutral amino acid transporter 9 isoform 2
NM_001258287.1 NP_001245216.1 sodium-coupled neutral amino acid transporter 9 isoform 3
NM_001282429.1 NP_001269358.1 sodium-coupled neutral amino acid transporter 9 isoform 4
NM_001349382.1 NP_001336311.1 sodium-coupled neutral amino acid transporter 9 isoform 1
NM_001349383.1 NP_001336312.1 sodium-coupled neutral amino acid transporter 9 isoform 1
NM_001349384.1 NP_001336313.1 sodium-coupled neutral amino acid transporter 9 isoform 1
NM_001349385.1 NP_001336314.1 sodium-coupled neutral amino acid transporter 9 isoform 5
NM_173514.4 NP_775785.2 sodium-coupled neutral amino acid transporter 9 isoform 1

SLC38A9 Protein Structure

Aa_trans

Aa_trans: Transmembrane amino acid transporter protein (119 - 239)

Aa_trans

Aa_trans: Transmembrane amino acid transporter protein (299 - 557)

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  • 500
  • 561 a.a.
Protein Preferred Names Protein Names

sodium-coupled neutral amino acid transporter 9

putative sodium-coupled neutral amino acid transporter 9

Related Diseases

Diseases Alias
Leukodystrophy, Hypomyelinating, 3

Hypomyelinating Leukodystrophy 3

HLD3

Pelizaeus-Merzbacher-Like Disease Due To Aimp1 Mutation

Leukodystrophy, Hypomyelinating 3

Perinatal Sudanophilic Leukodystrophy

Leukodystrophy, Hypomyelinating, Type 3

Pelizaeus-Merzbacher-Like Disease, Autosomal Recessive, 2
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-RS13227 SLC38A9 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus SLC38A9 MGD MGI:1918839
Felis catus SLC38A9 VGNC VGNC:65352
Bos taurus SLC38A9 VGNC VGNC:34856
Canis familiaris SLC38A9 VGNC VGNC:46399
Rattus norvegicus SLC38A9 RGD RGD:1311881
Macaca mulatta SLC38A9 VGNC VGNC:77574