Slc15a2 - solute carrier family 15 (H+/peptide transporter), member 2 Gene

Also Known as Pept2; 8430408C16Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 57738

Summary

Enables dipeptide transmembrane transporter activity and high-affinity oligopeptide transmembrane transporter activity. Involved in several processes, including dipeptide import across plasma membrane; peptidoglycan transport; and regulation of nucleotide-binding activity oligomerization domain containing signaling pathway. Acts upstream of or within oligopeptide transport. Located in membrane. Is integral component of plasma membrane. Is expressed in several structures, including genitourinary system; integumental system; nervous system; nose; and respiratory system. Orthologous to human SLC15A2 (solute carrier family 15 member 2). [provided by Alliance of Genome Resources, Apr 2022]

Slc15a2 Products (2)

mRNA Protein Name
NM_001145899.2 NP_001139371.2 solute carrier family 15 member 2 isoform 2
NM_021301.4 NP_067276.3 solute carrier family 15 member 2 isoform 1

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables dipeptide transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
29784761 MGI
enables high-affinity oligopeptide transmembrane transporter activity IDA
IDA: Inferred from direct assay
11027540 MGI
Biological Process GO Annotation Evidence References Source
involved in dipeptide import across plasma membrane IMP
IMP: Inferred from mutant phenotype
29784761 MGI
involved in dipeptide transport IMP
IMP: Inferred from mutant phenotype
17452417 MGI
acts upstream of or within oligopeptide transport IDA
IDA: Inferred from direct assay
11027540 MGI
involved in peptidoglycan transport IMP
IMP: Inferred from mutant phenotype
29784761 MGI
involved in regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway IMP
IMP: Inferred from mutant phenotype
29784761 MGI
involved in renal absorption IMP
IMP: Inferred from mutant phenotype
17452417 MGI
involved in xenobiotic transport IMP
IMP: Inferred from mutant phenotype
17452417 MGI
Cellular Component GO Annotation Evidence References Source
located in membrane IDA
IDA: Inferred from direct assay
11027540 MGI
located in plasma membrane IDA
IDA: Inferred from direct assay
11027540 MGI
located in plasma membrane IMP
IMP: Inferred from mutant phenotype
29784761 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

solute carrier family 15 member 2

  • kidney H(+)/peptide cotransporter

  • peptide transporter 2

  • proton-dependent high affinity oligopeptide transporter PepT2

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13013 SLC15A2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc15a2 NCBI NCBI:6565