Bbs1 Gene Summary [Rat]

Predicted to enable RNA polymerase II-specific DNA-binding transcription factor binding activity; phosphoprotein binding activity; and signaling receptor binding activity. Predicted to be involved in several processes, including non-motile cilium assembly; photoreceptor cell maintenance; and regulation of cilium beat frequency involved in ciliary motility. Predicted to act upstream of or within several processes, including Golgi to plasma membrane protein transport; nervous system development; and olfactory behavior. Predicted to be located in centriolar satellite; ciliary membrane; and motile cilium. Predicted to be part of BBSome. Predicted to be active in axoneme and centrosome. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome and Bardet-Biedl syndrome 1. Orthologous to human BBS1 (Bardet-Biedl syndrome 1). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Bbs1
Official Name
Bardet-Biedl syndrome 1 [Source:RGD Symbol;Acc:1307581]
Ensembl ID
ENSRNOG00000019832
Bio databases IDs NCBI: 309156 Ensembl: ENSRNOG00000019832
Aliases Bardet-Biedl syndrome 1
Synonyms AI451249, Bardet-Biedl syndrome 1, BBS2L2, D19Ertd609e
Species
Rat, Rattus norvegicus
OrthologiesHumanMouse

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Bbs1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • smoothened binding
  • phosphoprotein binding
  • transcription factor binding
  • protein binding
  • receptor binding
  • Ciliary BBSome complex subunit 1
  • patched binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • Bardet-Biedl syndrome type 1
  • Bardet-Biedl syndrome
  • weight gain
  • obesity
  • retinal dystrophy
  • digenic Bardet-Biedl syndrome 1/7
  • ciliopathy
  • retinitis pigmentosa
  • impaired glucose tolerance
  • cholesteatoma
regulated by
role in cell
  • phosphorylation in
  • migration
  • proliferation
  • quantity
  • morphology
  • morphogenesis
  • organization
  • stabilization
  • maintenance
  • assembly

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Extracellular Space
  • motile cilia
  • Cytoplasm
  • cilia
  • basal bodies
  • centrosome
  • cytosol

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the rat Bbs1 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • cilium morphogenesis
  • photoreceptor cell morphogenesis
  • neural precursor cell proliferation
  • regulation of cilium beat frequency involved in ciliary motility
  • fertilization
  • Golgi to plasma membrane protein transport
  • cellular lipid metabolic process
  • hippocampus development
  • brain morphogenesis
  • striatum development
  • microtubule cytoskeleton organization
  • cerebral cortex development
  • fat cell differentiation
  • visual perception
  • olfactory behavior
  • hormone metabolic process
  • ventricular system development
  • neuron migration
  • photoreceptor cell maintenance
  • sensory perception of smell
  • adult behavior
  • cartilage development
  • dendrite development

Cellular Component

Where in the cell the gene product is active
  • centrosome
  • motile cilium
  • BBSome
  • centriolar satellite
  • cytosol
  • cilium membrane
  • axoneme

Molecular Function

What the gene product does at the molecular level
  • protein binding
  • smoothened binding
  • phosphoprotein binding
  • patched binding

Gene-Specific Assays for Results You Can Trust

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