Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: BGN ENSPTRG00000022541

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Description

biglycan [Source:VGNC Symbol;Acc:VGNC:55703]

Location

Chromosome X: 153,161,211-153,176,102 forward strand.

Pan_tro_3.0:CM000336.3

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000043244.3	BGN-202	1131	376aa	ENSPTRP00000042754.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2R1R5	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,
ENSPTRT00000097530.1	BGN-201	2567	368aa	ENSPTRP00000066574.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W4S2 K7DR91	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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