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 contribute to ubiquitin protein ligase activity. Predicted to be involved in several processes, including G2/M transition of mitotic cell cycle; SCF-dependent proteasomal ubiquitin-dependent protein catabolic process; and entrainment of circadian clock by photoperiod. Predicted to localize to SCF ubiquitin ligase complex; 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