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

Gene: Mycl ENSRNOG00000014259

Description

MYCL proto-onco, bHLH transcription factor [Source:RGD Symbol;Acc:1588591]

Gene Synonyms

Lmyc1, Mycl1, Mycl1_mapped

Location

GRCr8:CM070395.1

About this gene

This gene has 1 transcript (splice variant), 268 orthologues, 4 paralogues and is associated with 3 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000019101.7	Mycl-201	3294	399aa	ENSRNOP00000019101.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V7T4	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,

Upcoming Ensembl Platform Transition