NPBWR1

protein-coding

neuropeptides B and W receptor 1, the group of Neuropeptides B and W receptors

Gene summary

Predicted to enable G protein-coupled receptor activity and neuropeptide binding activity. Involved in G protein-coupled receptor signaling pathway. Predicted to be located in membrane. Predicted to be active in neuron projection and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]

Previous symbols:
  • GPR7

MANE transcript

NM_005285.5

Inheritance

—

ClinVar variants

U:51B:4

Top phenotype

—

Max pathogenic AF

—

Genomic locus

chr8:52,939,182-52,943,734

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~4.6 kb
Loading mutation effect viewer...

GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to NPBWR1 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 54
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_005285.5. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
51
clinvar
3
clinvar
1
clinvar
55
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00513155
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 3 of 3 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_005285.5RefSeqNP_005276.21MANE Select
ENST00000674939.1EnsemblENSP00000501711.11MANE Select
ENST00001122477.1EnsemblENSP00000792282.11Standard
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.