Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4889
Gene name Gene Name - the full gene name approved by the HGNC.
Neuropeptide Y receptor Y5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NPY5R
Synonyms (NCBI Gene) Gene synonyms aliases
NPY5-R, NPYR5, NPYY5-R
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q32.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a receptor for neuropeptide Y and peptide YY. The encoded protein appears to be involved in regulating food intake, with defects in this gene being associated with eating disorders. Also, the encoded protein is involved
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1191810 hsa-miR-106a CLIP-seq
MIRT1191811 hsa-miR-106b CLIP-seq
MIRT1191812 hsa-miR-17 CLIP-seq
MIRT1191813 hsa-miR-20a CLIP-seq
MIRT1191814 hsa-miR-20b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001601 Function Peptide YY receptor activity IBA 21873635
GO:0001602 Function Pancreatic polypeptide receptor activity IBA 21873635
GO:0002675 Process Positive regulation of acute inflammatory response IEA
GO:0002865 Process Negative regulation of acute inflammatory response to antigenic stimulus IEA
GO:0003151 Process Outflow tract morphogenesis IMP 19593212
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602001 7958 ENSG00000164129
Protein
UniProt ID Q15761
Protein name Neuropeptide Y receptor type 5 (NPY5-R) (NPY-Y5 receptor) (NPYY5-R) (Y5 receptor)
Protein function Receptor for neuropeptide Y and peptide YY. The activity of this receptor is mediated by G proteins that inhibit adenylate cyclase activity. Seems to be associated with food intake. Could be involved in feeding disorders.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 58 425 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Brain; hypothalamus.
Sequence
Sequence length 445
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 (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Obesity Obesity rs74315349, rs1474810899, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562
View all (27 more)
10849579
Associations from Text Mining
Disease Name Relationship Type References
Alcohol Withdrawal Seizures Associate 18828811
Alcoholism Associate 18828811
Autistic Disorder Associate 15090072
Breast Neoplasms Associate 35093384
Carcinoma Renal Cell Associate 32788609
Diabetes Mellitus Inhibit 22029806
Dyslipidemias Associate 17426313, 20797317
Hypertension Associate 19593212
Hypertrophy Left Ventricular Associate 19593212
Hypoxia Stimulate 35093384, 35484119