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

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Gene: BSX ENSSSCG00000015139

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Description

brain specific homeobox [Source:VGNC Symbol;Acc:VGNC:85898]

Location

Primary_assembly 9: 49,905,428-49,909,226 reverse strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 1 transcript (splice variant), 126 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000016505.2	BSX-201	699	232aa	ENSSSCP00000016062.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VIV4 F1S9Q4	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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