NTS (Neurotensin) Gene

A comprehensive resource for the NTS gene, including genomic data, expression, mutations, and associated diseases.

Gene Information Card

Symbol NTS
Full Name Neurotensin
Gene Type protein-coding
Chromosomal Location 12q21.31
NCBI Gene ID 4922 ncbi.nlm.nih.gov/gene/4922
Ensembl ID ENSG00000133636
UniProt ID P30990
OMIM ID 162650
HGNC ID 8038
Aliases NT, NTS1, NN

Description

The NTS gene encodes neurotensin, a 13-amino acid neuropeptide that functions as a neurotransmitter and neuromodulator in the central nervous system and as a hormone in the periphery. It is involved in dopamine signaling, pain modulation, and gut motility. NTS is also implicated in cancer, where it can promote cell proliferation and migration.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal Cancer NTS overexpression activates MAPK and PI3K/Akt pathways, promoting tumor growth and metastasis. PMID: 23454750
Breast Cancer NTS signaling through NTSR1 enhances cell proliferation and invasion in estrogen receptor-positive breast cancer. PMID: 21575863
Schizophrenia Altered NTS levels in cerebrospinal fluid and brain regions are associated with dopamine dysregulation. PMID: 10446204
Irritable Bowel Syndrome NTS modulates intestinal motility and secretion, contributing to symptoms. PMID: 11083470

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.3 Medium
Small Intestine 8.7 Medium
Colon 6.5 Low
Stomach 5.2 Low
Pancreas 3.1 Low
Cell Line Expression
Cell Line nTPM Notes
SH-SY5Y 15.4 Neuroblastoma cell line; high NTS expression
HT-29 9.8 Colorectal adenocarcinoma; moderate expression
MCF-7 7.2 Breast cancer; moderate expression
HeLa 2.1 Cervical cancer; low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.79G>A (p.Glu27Lys) Missense <0.01% Unknown; rare variant in population databases
c.214C>T (p.Arg72Trp) Missense <0.01% Unknown; rare variant in population databases
c.315_316insA Frameshift <0.01% Predicted loss of function; not observed in ClinVar
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., c.315_316insA) are predicted to cause loss of function due to premature truncation.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in NTS.

Dominant Negative (DN)

No evidence for dominant-negative effects in NTS.

Pathways

• Neurotensin signaling pathway (Reactome: R-HSA-416476)
• GPCR downstream signaling (Reactome: R-HSA-388396)

Protein Summary

Neurotensin is a 13-amino acid peptide (sequence: pELYENKPRRPYIL) derived from a 170-amino acid precursor. It binds to three receptors: NTSR1, NTSR2, and NTSR3 (sortilin). The peptide modulates dopamine transmission, pain perception, and gut function. In cancer, NTS acts as a growth factor via NTSR1, activating MAPK and PI3K pathways.

Related Products

Product name Cat.No. Species Gene ID
NTSR1 Knockout HEK293 Cell Line EDJ-KQ1594 Human 4923 Details Get a Quote
NTS Knockout HEK293 Cell Line EDJ-KQ2476 Human 4922 Details Get a Quote
NTSR2 Knockout HEK293 Cell Line EDJ-KQ7426 Human 23620 Details Get a Quote
NTS Knockout A-549 Cell Line EDJ-KQ23044 Human 4922 Details Get a Quote
NTSR1 Knockout HCT 116 Cell Line EDJ-KQ21278 Human 4923 Details Get a Quote
NTS Knockout HeLa Cell Line EDJ-KQ21689 Human 4922 Details Get a Quote
NTSR1 Knockout HeLa Cell Line EDJ-KQ54034 Human 4923 Details Get a Quote
NTSR2 Knockout HeLa Cell Line EDJ-KQ55784 Human 23620 Details Get a Quote
NTSR1 Knockout A-549 Cell Line EDC90450 Human 4923 Details Get a Quote
NTSR2 Knockout A-549 Cell Line EDJ-KQ64279 Human 23620 Details Get a Quote
NTS Knockout HCT 116 Cell Line EDJ-KQ70993 Human 4922 Details Get a Quote
NTSR2 Knockout HCT 116 Cell Line EDJ-KQ72725 Human 23620 Details Get a Quote
Contact Us
*
*
*
How did you hear about us: