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NTS (neurotensin)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4922
Gene nameGene Name - the full gene name approved by the HGNC.
Neurotensin
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
NTS
SynonymsGene synonyms aliases
NMN-125, NN, NT, NT/N, NTS1
ChromosomeChromosome number
12
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q21.31
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a common precursor for two peptides, neuromedin N and neurotensin. Neurotensin is a secreted tridecapeptide, which is widely distributed throughout the central nervous system, and may function as a neurotransmitter or a neuromodulator. I
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1196318 hsa-miR-181a CLIP-seq
MIRT1196319 hsa-miR-181b CLIP-seq
MIRT1196320 hsa-miR-181c CLIP-seq
MIRT1196321 hsa-miR-181d CLIP-seq
MIRT1196322 hsa-miR-4262 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
ATF1 Unknown 7791794
CREB1 Unknown 7791794
FOS Unknown 7791794
JUN Unknown 7791794
JUND Unknown 7791794
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005184 Function Neuropeptide hormone activity IEA
GO:0005515 Function Protein binding IPI 17620610, 32296183
GO:0005576 Component Extracellular region TAS
GO:0007165 Process Signal transduction NAS 8954810
GO:0007186 Process G protein-coupled receptor signaling pathway TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P30990
Protein name Neurotensin/neuromedin N [Cleaved into: Large neuromedin N (NmN-125); Neuromedin N (NN) (NmN); Neurotensin (NT); Tail peptide]
Protein function Neurotensin may play an endocrine or paracrine role in the regulation of fat metabolism. It causes contraction of smooth muscle.
PDB 2LNE , 2LNF , 2LNG , 2LYW , 2OYV , 2OYW , 3F6K , 4PO7 , 5LUZ , 6UP7 , 8VJY
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07421 Pro-NT_NN
7 170
Neurotensin/neuromedin N precursor
Family
Sequence
Sequence length 170
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Neuroactive ligand-receptor interaction   Peptide ligand-binding receptors
G alpha (q) signalling events
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Schizophrenia Schizophrenia rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 20659557, 23483448, 25449842, 20193696
Unknown
Disease name Disease term dbSNP ID References
Catalepsy Catalepsy 20882060
Mental depression Mental Depression, Depressive disorder rs587778876, rs587778877 22754041
Mood disorder Mood Disorders 22754041

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