Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
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Gene: Bbs7 ENSRNOG00000015816

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Description

Bardet-Biedl syndrome 7 [Source:RGD Symbol;Acc:1309264]

Gene Synonyms

LOC361930

Location

Primary_assembly 2: 121,362,885-121,402,473 reverse strand.

GRCr8:CM070392.1

About this gene

This gene has 3 transcripts (splice variants), 199 orthologues and is associated with 10 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021453.8	Bbs7-201	2619	690aa	ENSRNOP00000021453.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q66H90	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,
ENSRNOT00000112087.2	Bbs7-203	2713	689aa	ENSRNOP00000081105.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G5H8	-
ENSRNOT00000111410.2	Bbs7-202	2153	683aa	ENSRNOP00000079415.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZN21	-

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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data