Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Des ENSRNOG00000019810

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Description

desmin [Source:RGD Symbol;Acc:620686]

Location

Primary_assembly 9: 76,850,982-76,858,699 forward strand.

mRatBN7.2:CM026982.1

About this gene

This gene has 2 transcripts (splice variants), 280 orthologues, 69 paralogues and is associated with 46 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000026860.5	Des-201	2163	469aa	ENSRNOP00000026860.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6P725	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,
ENSRNOT00000117593.1	Des-202	2485	468aa	ENSRNOP00000094817.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ANC1	-

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Summary

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