Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
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Ontologies
Phenotypes
Genetic Variation
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Pathway
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External references
Supporting evidence
ID History
- Gene history

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Gene: BBS2 ENSSSCG00000025417

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Description

Bardet-Biedl syndrome 2 [Source:HGNC Symbol;Acc:HGNC:967]

Location

Primary_assembly 6: 18,542,386-18,575,514 reverse strand.

Sscrofa11.1:CM000817.5

About this gene

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

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000024678.4	BBS2-202	2719	727aa	ENSSSCP00000027274.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	I3LT30	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,
ENSSSCT00000082172.1	BBS2-201	2577	683aa	ENSSSCP00000068782.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R3K8	-

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Summary

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