Gene Gene information from NCBI Gene database.
Entrez ID 4923
Gene name Neurotensin receptor 1
Gene symbol NTSR1
Synonyms (NCBI Gene)
NTR
Chromosome 20
Chromosome location 20q13.33
Summary Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secre
miRNA miRNA information provided by mirtarbase database.
173
miRTarBase ID miRNA Experiments Reference
MIRT017517 hsa-miR-335-5p Microarray 18185580
MIRT029363 hsa-miR-26b-5p Microarray 19088304
MIRT1196327 hsa-miR-1231 CLIP-seq
MIRT1196328 hsa-miR-1254 CLIP-seq
MIRT1196329 hsa-miR-1275 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
68
GO ID Ontology Definition Evidence Reference
GO:0001659 Process Temperature homeostasis IEA
GO:0003085 Process Negative regulation of systemic arterial blood pressure IEA
GO:0003254 Process Regulation of membrane depolarization IEA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 8381365
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
162651 8039 ENSG00000101188
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P30989
Protein name Neurotensin receptor type 1 (NT-R-1) (NTR1) (High-affinity levocabastine-insensitive neurotensin receptor) (NTRH)
Protein function G-protein coupled receptor for the tridecapeptide neurotensin (NTS) (PubMed:21725197, PubMed:23140271, PubMed:8381365). Signaling is effected via G proteins that activate a phosphatidylinositol-calcium second messenger system. Signaling leads to
PDB 2LYW , 6OS9 , 6OSA , 6PWC , 6UP7 , 7UL2 , 8JPB , 8JPC , 8JPF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 80 364 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in prostate (at protein level). Detected in colon and peripheral blood mononuclear cells. Detected at very low levels in brain. {ECO:0000269|PubMed:20048080, ECO:0000269|PubMed:8381365}.
Sequence
Sequence length 418
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
  Peptide ligand-binding receptors
G alpha (q) signalling events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
5
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs59757062 RCV005912034
Gastric cancer Benign rs34864360 RCV005904998
Ovarian serous cystadenocarcinoma Benign rs59757062 RCV005912035
Uterine carcinosarcoma Benign rs34864360 RCV005904999
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acidosis Associate 19393580
Adenocarcinoma of Lung Associate 36439693
Adenomatous Polyposis Coli Associate 26215716
Alzheimer Disease Associate 11927634, 22142809
Alzheimer Disease Inhibit 16539663, 21397006
Anophthalmia with pulmonary hypoplasia Associate 36949141
Brain Neoplasms Associate 30959962
Breast Neoplasms Associate 11359788, 19156213, 21725197, 22161836, 27388253
Carcinogenesis Associate 26298774
Carcinoid Tumor Associate 26298774