Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: NPBWR2 ENSSSCG00000037868

.

Description

neuropeptides B and W receptor 2 [Source:VGNC Symbol;Acc:VGNC:110574]

Location

Primary_assembly 17: 62,917,322-62,918,320 reverse strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 1 transcript (splice variant), 145 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000045438.2	NPBWR2-201	999	333aa	ENSSSCP00000039175.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287A5D3	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

.

Summary

.

.