Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4923
Gene name Gene Name - the full gene name approved by the HGNC.
Neurotensin receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NTSR1
Synonyms (NCBI Gene) Gene synonyms aliases
NTR
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 TAS 8381365
GO:0005515 Function Protein binding IPI 17620610, 23597562, 23624386
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
162651 8039 ENSG00000101188
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism spectrum disorder Autism Spectrum Disorders rs724159978, rs75184679, rs119103221, rs9332964, rs121912562, rs1594344233, rs727504317, rs111033204, rs1801086, rs587784464, rs724159948, rs764659822, rs794727977, rs796052733, rs796052728
View all (51 more)
24781735
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
20659557
Associations from Text Mining
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