Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
121260
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 15 member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC15A4
Synonyms (NCBI Gene) Gene synonyms aliases
FP12591, PHT1, PTR4
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.33
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT002585 hsa-miR-124-3p Microarray 15685193
MIRT002585 hsa-miR-124-3p Microarray 15685193
MIRT002585 hsa-miR-124-3p Microarray 18668037
MIRT044921 hsa-miR-186-5p CLASH 23622248
MIRT038188 hsa-miR-151a-5p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005290 Function L-histidine transmembrane transporter activity IBA 21873635
GO:0005290 Function L-histidine transmembrane transporter activity IDA 25238095, 29224352
GO:0005515 Function Protein binding IPI 24695226, 32433612
GO:0005765 Component Lysosomal membrane TAS
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615806 23090 ENSG00000139370
Protein
UniProt ID Q8N697
Protein name Solute carrier family 15 member 4 (Peptide transporter 4) (Peptide/histidine transporter 1) (hPHT1)
Protein function Proton-coupled amino-acid transporter that mediates the transmembrane transport of L-histidine and some di- and tripeptides from inside the lysosome to the cytosol, and plays a key role in innate immune response (PubMed:16289537, PubMed:25238095
PDB 8JZR , 8JZS , 8JZU , 8JZX , 8P6A , 8QSK , 8QSL , 8QSM , 8QSN , 8WX3 , 8WX4 , 8WX5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00854 PTR2 103 518 POT family Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in skeletal muscle. Moderately expressed in kidney, liver, and heart. Weakly expressed in colon and brain. Expressed in low levels throughout the gastrointestinal tract and in Caco-2 cells. Expressed in retinal fragmen
Sequence
Sequence length 577
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Proton/oligopeptide cotransporters
Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Systemic lupus erythematosus Systemic lupus erythematosus GWAS
Associations from Text Mining
Disease Name Relationship Type References
Colitis Ulcerative Associate 37445676
Colorectal Neoplasms Associate 35562597
Combined Pituitary Hormone Deficiency Associate 29261175
Inflammation Associate 37445676
Inflammatory Bowel Diseases Stimulate 19570976
Lupus Erythematosus Systemic Associate 27362648, 31001245
Neoplasms Associate 35562597
Prostatic Neoplasms Associate 11742494, 22950754
Prostatitis Associate 11742494
Sjogren's Syndrome Associate 31001245