Gene
fbxl3b
- ID
- ZDB-GENE-041010-178
- Name
- F-box and leucine-rich repeat protein 3b
- Symbol
- fbxl3b Nomenclature History
- Previous Names
-
- wu:fd52d09
- zgc:101682
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to be involved in SCF-dependent proteasomal ubiquitin-dependent protein catabolic process and entrainment of circadian clock by photoperiod. Predicted to be part of SCF ubiquitin ligase complex. Predicted to be active in cytosol and nucleus. Orthologous to human FBXL3 (F-box and leucine rich repeat protein 3).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Intellectual developmental disorder with short stature, facial anomalies, and speech defects | 606220 |
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | F-box domain | F-box-like domain superfamily | Leucine-rich repeat domain superfamily |
---|---|---|---|---|
UniProtKB:Q5XJQ3
|
162 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available