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: Mynn ENSRNOG00000027923

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Description

myoneurin [Source:RGD Symbol;Acc:1307889]

Gene Synonyms

LOC361924, MGC108895

Location

Primary_assembly 2: 114,708,156-114,725,452 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 154 orthologues, 56 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000078148.3	Mynn-202	4204	610aa	ENSRNOP00000075326.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2KAA6 A6IHM0	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,
ENSRNOT00000010344.8	Mynn-201	4120	582aa	ENSRNOP00000010344.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IHL9 F7F7X6	-

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Summary

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