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

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Gene: MYT1 ENSSSCG00000039212

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Description

myelin transcription factor 1 [Source:VGNC Symbol;Acc:VGNC:104000]

Location

Primary_assembly 17: 62,979,350-63,014,696 forward strand.

Sscrofa11.1:CM000828.5

About this gene

This gene has 2 transcripts (splice variants), 274 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000054739.3	MYT1-202	5049	1116aa	ENSSSCP00000035817.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZW30 A0A8D0TFH7	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,
ENSSSCT00000053867.3	MYT1-201	1770	590aa	ENSSSCP00000036547.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZY54 A0A8D0TE38	-

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Summary

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