Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
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: BBS5 ENSPTRG00000012614

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Description

Bardet-Biedl syndrome 5 [Source:HGNC Symbol;Acc:HGNC:970]

Location

Chromosome 2B: 59,657,380-59,682,963 forward strand.

Pan_tro_3.0:CM000316.3

About this gene

This gene has 2 transcripts (splice variants) and 193 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000023364.5	BBS5-202	1705	341aa	ENSPTRP00000021547.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	K7CV40	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,
ENSPTRT00000087256.1	BBS5-201	1643	320aa	ENSPTRP00000063140.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3REP2	-

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Summary

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