Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
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: Myef2 ENSRNOG00000005258

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Description

myelin expression factor 2 [Source:RGD Symbol;Acc:1306547]

Gene Synonyms

LOC362207, MGC109392

Location

Primary_assembly 3: 132,791,694-132,827,523 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 5 transcripts (splice variants), 218 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000081533.3	Myef2-203	2945	591aa	ENSRNOP00000072845.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K402	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 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,
ENSRNOT00000007103.8	Myef2-201	2894	574aa	ENSRNOP00000007103.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AEI5	-
ENSRNOT00000099942.2	Myef2-204	2873	567aa	ENSRNOP00000077919.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y9T8	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,
ENSRNOT00000109676.2	Myef2-205	2846	558aa	ENSRNOP00000081666.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZTD6	-
ENSRNOT00000043611.5	Myef2-202	2774	534aa	ENSRNOP00000048644.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZFG9	-

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Summary

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