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

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Gene: heyl ENSDARG00000055798

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Description

hes related family bHLH transcription factor with YRPW motif like [Source:NCBI gene;Acc:335134]

Gene Synonyms

fk74e12, wu:fk74e12

Location

Chromosome 19: 32,553,874-32,560,591 forward strand.

GRCz11:CM002903.2

About this gene

This gene has 1 transcript (splice variant), 285 orthologues and 27 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000078197.5	heyl-201	1619	310aa	ENSDARP00000072659.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q8AXV5	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,

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Summary

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