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: Myo5c ENSRNOG00000008356

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Description

myosin VC [Source:RGD Symbol;Acc:1309994]

Gene Synonyms

LOC315820

Location

Primary_assembly 8: 75,989,528-76,066,483 forward strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 1 transcript (splice variant), 218 orthologues, 41 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000011768.8	Myo5c-201	6640	1749aa	ENSRNOP00000011768.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M111	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,

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Summary

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