Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: myt1la ENSDARG00000008209

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Description

myelin transcription factor 1-like, a [Source:ZFIN;Acc:ZDB-GENE-041001-172]

Location

Chromosome 20: 30,445,971-30,574,029 forward strand.

GRCz11:CM002904.2

About this gene

This gene has 2 transcripts (splice variants), 78 orthologues, 7 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000153150.3	myt1la-201	4144	1257aa	ENSDARP00000127218.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5TZG3	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,
ENSDART00000184871.1	myt1la-202	3803	1257aa	ENSDARP00000154337.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5TZG3	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,

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Summary

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