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

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Gene: nmur3 ENSDARG00000022570

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Description

neuromedin U receptor 1 [Source:HGNC Symbol;Acc:HGNC:4518]

Location

Chromosome 11: 28,107,632-28,126,139 forward strand.

GRCz11:CM002895.2

About this gene

This gene has 2 transcripts (splice variants), 170 orthologues, 22 paralogues and is associated with 6 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000028641.9	nmur3-201	1340	424aa	ENSDARP00000031354.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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, 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000177721.2	nmur3-202	5448	392aa	ENSDARP00000144357.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286YBK1	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,

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Summary

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