Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Gene: Bbs2 ENSRNOG00000019020

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Description

Bardet-Biedl syndrome 2 [Source:RGD Symbol;Acc:71091]

Location

Primary_assembly 19: 10,915,476-10,950,921 forward strand.

GRCr8:CM070409.1

About this gene

This gene has 2 transcripts (splice variants), 202 orthologues and is associated with 14 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000106411.2	Bbs2-202	2746	740aa	ENSRNOP00000087643.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A3J2	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,
ENSRNOT00000026076.5	Bbs2-201	2725	675aa	ENSRNOP00000026076.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q99MH9	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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