NMUR2 (neuromedin U receptor 2)
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.
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
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
|
||||||||||
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.
|
|||||||||
|
Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
|
|||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||
|