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
External references
Supporting evidence
ID History
- Gene history

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Gene: Myom1 ENSRNOG00000057701

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Description

myomesin 1 [Source:RGD Symbol;Acc:631436]

Location

Primary_assembly 9: 118,362,621-118,485,952 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 4 transcripts (splice variants), 271 orthologues, 13 paralogues and is associated with 15 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000112958.2	Myom1-203	5716	1689aa	ENSRNOP00000085118.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GBP8	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 P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000173417.1	Myom1-204	5592	1592aa	ENSRNOP00000101346.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000095102.2	Myom1-202	5233	1545aa	ENSRNOP00000087945.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GFM8	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSRNOT00000085362.3	Myom1-201	5202	1676aa	ENSRNOP00000073506.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K5P5	-

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Summary

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