Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: NMS ENSCAFG00845016126

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Description

neuromedin S [Source:HGNC Symbol;Acc:HGNC:32203]

Location

Primary_assembly 10: 43,126,855-43,140,936 reverse strand.

ROS_Cfam_1.0:CM025109.1

About this gene

This gene has 1 transcript (splice variant) and 87 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00845028687.1	NMS-201	887	147aa	ENSCAFP00845022579.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I3P1U0	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,

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Summary

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