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: BARX1 ENSPTRG00000021129

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Description

BARX homeobox 1 [Source:VGNC Symbol;Acc:VGNC:4624]

Location

Chromosome 9: 71,697,409-71,701,139 reverse strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 1 transcript (splice variant), 195 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000039082.5	BARX1-201	1513	254aa	ENSPTRP00000047016.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y061 H2R4D7	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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