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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HESX1 ENSPTRG00000015044

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Description

HESX homeobox 1 [Source:VGNC Symbol;Acc:VGNC:1836]

Location

Chromosome 3: 58,358,122-58,387,583 reverse strand.

Pan_tro_3.0:CM000317.3

About this gene

This gene has 2 transcripts (splice variants), 195 orthologues and 58 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000028167.4	HESX1-201	2020	185aa	ENSPTRP00000025986.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8P7U0 A2T777	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,
ENSPTRT00000108118.1	HESX1-202	456	151aa	ENSPTRP00000079824.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SS96 A0A6D2WH69	-

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Summary

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