Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Ontologies
- GO: Anatomical entity
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Genetic Variation
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ID History
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Gene: NMS ENSRNOG00000038979

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Description

neuromedin S [Source:RGD Symbol;Acc:1359122]

Location

Primary_assembly 9: 48,665,398-48,676,461 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 3 transcripts (splice variants) and 86 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000157217.1	NMS-203	557	173aa	ENSRNOP00000101925.1	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,
ENSRNOT00000149399.1	NMS-202	533	165aa	ENSRNOP00000111288.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000059587.4	NMS-201	496	152aa	ENSRNOP00000056345.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5H8A2	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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