Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Myg1 ENSRNOG00000013343

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Description

MYG1 exonuclease [Source:RGD Symbol;Acc:1359237]

Gene Synonyms

C12orf10, MGC95325

Location

Primary_assembly 7: 135,335,334-135,346,740 forward strand.

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000017942.8	Myg1-201	1192	381aa	ENSRNOP00000017942.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q641W2	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,
ENSRNOT00000136838.1	Myg1-202	1127	362aa	ENSRNOP00000111052.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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