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

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Gene: bgna ENSDARG00000017884

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Description

biglycan a [Source:ZFIN;Acc:ZDB-GENE-040704-74]

Gene Synonyms

bgn, zgc:91989

Location

Chromosome 8: 14,104,496-14,126,646 reverse strand.

GRCz11:CM002892.2

About this gene

This gene has 2 transcripts (splice variants), 137 orthologues and 30 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000027225.8	bgna-201	1719	369aa	ENSDARP00000017536.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6GMI5	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,
ENSDART00000184946.1	bgna-202	1131	369aa	ENSDARP00000156458.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6GMI5	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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