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

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Gene: bsx ENSDARG00000068976

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Description

brain-specific homeobox [Source:ZFIN;Acc:ZDB-GENE-040628-4]

Location

Chromosome 10: 29,890,535-29,892,486 reverse strand.

GRCz11:CM002894.2

About this gene

This gene has 1 transcript (splice variant), 229 orthologues, 11 paralogues and is associated with 49 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000099983.4	bsx-201	977	227aa	ENSDARP00000090755.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1LY36 Q6R3Q6	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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