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
  - Paralogues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
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External references
Supporting evidence
ID History
- Gene history

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Gene: BBS1 ENSSSCG00000040416

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Description

Bardet-Biedl syndrome 1 [Source:HGNC Symbol;Acc:HGNC:966]

Location

Primary_assembly 2: 5,886,990-5,906,388 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 3 transcripts (splice variants) and 188 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000042335.2	BBS1-202	3749	593aa	ENSSSCP00000035869.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZWI7 A0A8D1LGF4	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,
ENSSSCT00000080622.1	BBS1-203	3458	496aa	ENSSSCP00000073546.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2R8Z0 A0A8D1HKK7	-
ENSSSCT00000079927.2	BBS1-201	1639	536aa	ENSSSCP00000061919.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QIS0	-

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Summary

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