Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: HLF ENSGALG00010029244

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Description

HLF transcription factor, PAR bZIP family member [Source:UniProtKB Gene Name;Acc:A0A8V1AIZ9]

Location

Primary_assembly 18: 6,539,807-6,570,493 forward strand.

bGalGal1.mat.broiler.GRCg7b:CM028499.1

About this gene

This gene has 1 transcript (splice variant), 277 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGALT00010070691.1	HLF-201	1977	293aa	ENSGALP00010043382.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8V1AIZ9	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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