Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Nmu ENSRNOG00000002164

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Description

neuromedin U [Source:RGD Symbol;Acc:68388]

Location

Primary_assembly 14: 32,198,943-32,226,632 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 3 transcripts (splice variants), 142 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000159345.1	Nmu-203	641	174aa	ENSRNOP00000103523.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A250SHE5 P12760	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,
ENSRNOT00000113115.2	Nmu-202	1031	166aa	ENSRNOP00000097729.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6B657	-
ENSRNOT00000002941.6	Nmu-201	611	164aa	ENSRNOP00000002941.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2UHE1	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data