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
Gene expression
Pathway
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External references
Supporting evidence
ID History
- Gene history

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Gene: BBS7 ENSSSCG00000009093

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Description

Bardet-Biedl syndrome 7 [Source:HGNC Symbol;Acc:HGNC:18758]

Location

Primary_assembly 8: 102,213,455-102,259,204 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 2 transcripts (splice variants) and 198 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000009960.4	BBS7-202	3279	715aa	ENSSSCP00000009703.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A288CFV9	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,
ENSSSCT00000037761.2	BBS7-201	2805	693aa	ENSSSCP00000049949.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287B0K8	-

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Summary

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