Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6869
Gene name Gene Name - the full gene name approved by the HGNC.
Tachykinin receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TACR1
Synonyms (NCBI Gene) Gene synonyms aliases
NK1R, NKIR, SPR, TAC1R
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p12
Summary Summary of gene provided in NCBI Entrez Gene.
This gene belongs to a gene family of tachykinin receptors. These tachykinin receptors are characterized by interactions with G proteins and contain seven hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin substance P, al
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT736804 hsa-miR-206 Western blotting, Immunofluorescence 31579977
MIRT1408484 hsa-miR-1245b-3p CLIP-seq
MIRT1408485 hsa-miR-181a CLIP-seq
MIRT1408486 hsa-miR-181b CLIP-seq
MIRT1408487 hsa-miR-181c CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004995 Function Tachykinin receptor activity IBA 21873635
GO:0005515 Function Protein binding IPI 12716968, 17986524, 23597562, 32296183
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane IDA 17986524
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
162323 11526 ENSG00000115353
Protein
UniProt ID P25103
Protein name Substance-P receptor (SPR) (NK-1 receptor) (NK-1R) (Tachykinin receptor 1)
Protein function This is a receptor for the tachykinin neuropeptide substance P. It is probably associated with G proteins that activate a phosphatidylinositol-calcium second messenger system. The rank order of affinity of this receptor to tachykinins is: substa
PDB 2KS9 , 2KSA , 2KSB , 6E59 , 6HLL , 6HLO , 6HLP , 7P00 , 7P02 , 7RMG , 7RMH , 7RMI , 8U26
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 49 305 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 407
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
  Tachykinin receptors bind tachykinins
G alpha (q) signalling events
Cargo recognition for clathrin-mediated endocytosis
Clathrin-mediated endocytosis
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention Deficit Disorder, Attention deficit hyperactivity disorder rs786205019 19204064
Hypertension Hypertensive disease rs13306026 21294877
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder 16594257, 17974009, 24705689, 20112009, 12692775 ClinVar
Seborrheic dermatitis Seborrheic dermatitis GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Abdominal Pain Associate 23582152
Adenocarcinoma Associate 37385990
Alcoholism Associate 19553914, 24817687
Anorexia Nervosa Associate 28291261
Anxiety Associate 19545476, 37142998
Anxiety Inhibit 19553914
Anxiety Disorders Associate 28291261
Arthritis Psoriatic Associate 22089831
Arthritis Rheumatoid Associate 31010320, 9717978
Astrocytoma Associate 35950469