Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Myh3 ENSRNOG00000046276

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Description

myosin heavy chain 3 [Source:RGD Symbol;Acc:3138]

Gene Synonyms

RNMHCG

Location

Primary_assembly 10: 52,269,185-52,293,000 forward strand.

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 102 orthologues, 42 paralogues and is associated with 16 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000004147.7	Myh3-201	6035	1940aa	ENSRNOP00000004147.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HFH7 G3V6D8	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,
ENSRNOT00000115161.2	Myh3-202	5750	1875aa	ENSRNOP00000089035.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A7B8	-

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Summary

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