Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Gene: MYMX ENSPSNG00000021603

Description

myomixer, myoblast fusion factor [Source:HGNC Symbol;Acc:HGNC:52391]

Location

mPhoSin1.pri:CM018166.1

About this gene

This gene has 1 transcript (splice variant) and 60 orthologues.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPSNT00000033507.1	MYMX-201	255	84aa	ENSPSNP00000029865.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C9KXY8	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,

Summary