FBXO7
Sign in to saveAlso known as FBX, FBX07, FBX7, PARK15, PKPS, F-box protein 7
F-box only protein 7 is a protein that in humans is encoded by the FBXO7 gene. Mutations in FBXO7 have been associated with Parkinson's disease.
Gene data
FBXO7- Name
- F-box protein 7
- Type
- protein-coding
- Position
- 32,474,676–32,499,787 (+)
- Aliases
- FBX, FBX07, FBX7, PARK15, PKPS
- Ensembl
- ENSG00000100225
- RefSeq RNA
- NM_001033024.2, NM_001257990.2, NM_012179.4
- RefSeq protein
- NP_001028196.1, NP_001244919.1, NP_036311.3
This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of the ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the Fbxs class and it may play a role in regulation of hematopoiesis. Alternatively spliced transcript variants of this gene have been identified with the full-length natures of only some variants being determined. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
F-box protein 7
- Symbol
- FBXO7
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 22:32,474,676-32,499,787
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 8136
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/25793
- genomic end
- 32894818
- genomic start
- 32870663
- chromosome
- human chromosome 22
- cytogenetic location
- 22q12.3
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Function
- Interactions
- References
- Further reading
F-box only protein 7 is a protein that in humans is encoded by the FBXO7 gene. Mutations in FBXO7 have been associated with Parkinson's disease.
== Function ==
Excerpted from Wikipedia’s “FBXO7” article, available under the CC BY-SA 4.0 licence.