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  2. Npy5r - neuropeptide Y receptor Y5 Gene

Npy5r - neuropeptide Y receptor Y5 Gene

Rattus norvegicus

Also known as NPYR5

Gene ID: 25340 | Gene type: protein coding

About Npy5r

Cytogenetic location: 4q32.2 Genomic coordinates (GRCh38): 4:163,343,892-163,352,403 (from NCBI)

This gene has 3 transcripts (splice variants), 137 orthologues and 33 paralogues.

Summary

Enables pancreatic polypeptide receptor activity and peptide YY receptor activity. Involved in several processes, including generation of ovulation cycle rhythm; negative regulation of GABAergic synaptic transmission; and regulation of acute inflammatory response. Located in cytoplasm. Used to study childhood absence epilepsy; hyperinsulinism; and visual epilepsy. Biomarker of coronary restenosis; obesity; and prolactinoma. Human ortholog(s) of this gene implicated in lipid metabolism disorder and obesity. Orthologous to human NPY5R (Neuropeptide Y Receptor Y5). [provided by Alliance of Genome Resources, Apr 2022]

Npy5r Products(3)

mRNA Protein Name
NM_012869.2 NP_037001.1 neuropeptide Y receptor type 5
XM_006253014.4 XP_006253076.1 neuropeptide Y receptor type 5 isoform X1
NM_012869.2 NP_037001.1 neuropeptide Y receptor type 5
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables neuropeptide Y receptor activity IDA
IDA: Inferred from direct assay
8824284 RGD
enables pancreatic polypeptide receptor activity IDA
IDA: Inferred from direct assay
8824284 RGD
enables peptide YY receptor activity IDA
IDA: Inferred from direct assay
8824284 RGD
Biological Process GO Annotation Evidence Reference Source
involved in eating behavior IMP
IMP: Inferred from mutant phenotype
9795372 RGD
involved in generation of ovulation cycle rhythm IMP
IMP: Inferred from mutant phenotype
12047724 RGD
involved in negative regulation of acute inflammatory response to antigenic stimulus IDA
IDA: Inferred from direct assay
18805447 RGD
involved in negative regulation of apoptotic process IMP
IMP: Inferred from mutant phenotype
12791184 RGD
involved in negative regulation of glutamate secretion IMP
IMP: Inferred from mutant phenotype
12623227 RGD
involved in negative regulation of synaptic transmission, GABAergic IMP
IMP: Inferred from mutant phenotype
11796508 RGD
involved in positive regulation of ERK1 and ERK2 cascade IMP
IMP: Inferred from mutant phenotype
21595512 RGD
involved in positive regulation of acute inflammatory response IMP
IMP: Inferred from mutant phenotype
12161018 RGD
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
21595512 RGD
involved in positive regulation of smooth muscle cell proliferation IMP
IMP: Inferred from mutant phenotype
12710532 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

Npy5r Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (58 - 425)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 445 a.a.
Protein Preferred Names Protein Names

neuropeptide Y receptor type 5

NPY-Y5 receptor

NPY5-R

NPYY5-R

Neuropeptide Y5 receptor

Y5 receptor

Related Diseases

Diseases Alias
Panic Disorder

Panic Anxiety Syndrome

Panic

Panic Disorder 1

Episodic Paroxysmal Anxiety Disorder

Body Mass Index Quantitative Trait Locus 11

OBESITY

Obesity, Susceptibility To

Leanness, Inherited

Obesity, Susceptibility To, Bmiq11

Obesity, Mild, Early-Onset

Obesity, Association With

Obesity, Early-Onset, Susceptibility To

Obesity, Severe

Obesity, Severe, And Type Ii Diabetes

Obesity, Late-Onset

BMIQ11

Obesity Bmiq11

Obesity, Early-Onset

Obesity , Susceptibility To

Simple Obesity Nos

Excess Fat

Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

Adiposis

Neuroblastoma

Nb

Neuroblastoma, Susceptibility To

Neuroblastomas

Central Neuroblastoma

Dihydropyrimidinase Deficiency

Dihydropyrimidinuria

Dpys Deficiency

Dph Deficiency

DPYSD

Dihydrouracil Amidohydrolase Deficiency

Dihydropyrimidinuria Due To Dpys Deficiency

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Homo sapiens Npy5r NCBI NCBI:4889