Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6565
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 15 member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC15A2
Synonyms (NCBI Gene) Gene synonyms aliases
PEPT2
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
The mammalian kidney expresses a proton-coupled peptide transporter that is responsible for the absorption of small peptides, as well as beta-lactam antibiotics and other peptide-like drugs, from the tubular filtrate. This transporter, SLC15A2, belongs to
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023364 hsa-miR-122-5p Microarray 17612493
MIRT631111 hsa-miR-125a-3p HITS-CLIP 23824327
MIRT631110 hsa-miR-764 HITS-CLIP 23824327
MIRT631109 hsa-miR-3934-5p HITS-CLIP 23824327
MIRT631108 hsa-miR-4421 HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16738539, 32296183
GO:0005886 Component Plasma membrane IC 18367661, 18762712
GO:0005886 Component Plasma membrane ISS
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602339 10921 ENSG00000163406
Protein
UniProt ID Q16348
Protein name Solute carrier family 15 member 2 (Kidney H(+)/peptide cotransporter) (Oligopeptide transporter, kidney isoform) (Peptide transporter 2)
Protein function Proton-coupled amino-acid transporter that transports oligopeptides of 2 to 4 amino acids with a preference for dipeptides (PubMed:16434549, PubMed:18367661, PubMed:7756356). Transports neutral and anionic dipeptides with a proton to peptide sto
PDB 6EZI , 7PMY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00854 PTR2 111 487 POT family Family
PF00854 PTR2 566 675 POT family Family
Tissue specificity TISSUE SPECIFICITY: Expressed in kidney (PubMed:7756356). Not detected in intestine (PubMed:7756356). Highly expressed in macrophages (PubMed:20406817). {ECO:0000269|PubMed:20406817, ECO:0000269|PubMed:7756356}.
Sequence
Sequence length 729
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Proton/oligopeptide cotransporters
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Lung adenocarcinoma Adenocarcinoma of lung (disorder) rs28934576, rs121913530, rs397516975, rs587776805, rs121913469, rs121913364, rs121913351, rs121913366, rs397516896, rs397516977, rs397516981, rs397517127, rs121913344, rs727504233, rs121913370
View all (5 more)
27602772
Melanoma melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
22842228
Multiple sclerosis Multiple Sclerosis rs104895219, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039
View all (4 more)
21833088, 26920376
Unknown
Disease term Disease name Evidence References Source
Eczema Eczema GWAS
Multiple Sclerosis Multiple Sclerosis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 25965825
Chronic Kidney Disease Mineral and Bone Disorder Associate 27249515
Cystic Fibrosis Associate 11809991
Glioma Associate 30929128
Intellectual Disability Associate 39586343
Kidney Diseases Associate 28031405
Mitochondrial Diseases Associate 40286765
Multiple Myeloma Associate 31511451
Neoplasms Associate 40286765
Porphyria Acute Intermittent Associate 28031405