Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56923
Gene name Gene Name - the full gene name approved by the HGNC.
Neuromedin U receptor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NMUR2
Synonyms (NCBI Gene) Gene synonyms aliases
FM-4, FM4, NMU-R2, NMU2R, TGR-1, TGR1
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q33.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein from the G-protein coupled receptor 1 family. This protein is a receptor for neuromedin U, which is a neuropeptide that is widely distributed in the gut and central nervous system. This receptor plays an important role in the r
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1188107 hsa-miR-3616-5p CLIP-seq
MIRT1188108 hsa-miR-3647-5p CLIP-seq
MIRT1188109 hsa-miR-3663-3p CLIP-seq
MIRT1188110 hsa-miR-4795-5p CLIP-seq
MIRT1188111 hsa-miR-4797-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001607 Function Neuromedin U receptor activity IDA 10887190, 10894543
GO:0002023 Process Reduction of food intake in response to dietary excess IEA
GO:0004930 Function G protein-coupled receptor activity TAS 10894543
GO:0005229 Function Intracellular calcium activated chloride channel activity IDA 10899166
GO:0005515 Function Protein binding IPI 25416956
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605108 16454 ENSG00000132911
Protein
UniProt ID Q9GZQ4
Protein name Neuromedin-U receptor 2 (NMU-R2) (G-protein coupled receptor FM-4) (G-protein coupled receptor TGR-1)
Protein function Receptor for the neuromedin-U and neuromedin-S neuropeptides.
PDB 7W55 , 7W57 , 7XK8
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 62 327 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in the CNS, particularly in the medulla oblongata, pontine reticular formation, spinal cord, and thalamus. High level in testis whereas lower levels are present in a variety of peripheral tissues including the g
Sequence
Sequence length 415
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction   Peptide ligand-binding receptors
G alpha (q) signalling events
G alpha (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Migraine Migraine Disorders rs794727411 30266756
Associations from Text Mining
Disease Name Relationship Type References
Alcoholism Associate 21876473
Asthma Associate 36543808
Breast Neoplasms Associate 28423716
Carcinogenesis Associate 26317338
Colorectal Neoplasms Associate 34493299
Obesity Associate 36232539
Osteoarthritis Associate 36232539
Ovarian Neoplasms Associate 26317338
Pulmonary Disease Chronic Obstructive Inhibit 36543808
Rotator Cuff Injuries Associate 30424787