Gene Gene information from NCBI Gene database.
Entrez ID 26259
Gene name F-box and WD repeat domain containing 8
Gene symbol FBXW8
Synonyms (NCBI Gene)
FBW6FBW8FBX29FBXO29FBXW6
Chromosome 12
Chromosome location 12q24.22
Summary This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cul
miRNA miRNA information provided by mirtarbase database.
345
miRTarBase ID miRNA Experiments Reference
MIRT643228 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT643227 hsa-miR-1304-3p HITS-CLIP 23824327
MIRT643226 hsa-miR-2682-3p HITS-CLIP 23824327
MIRT643225 hsa-miR-6781-3p HITS-CLIP 23824327
MIRT643224 hsa-miR-604 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
40
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 15070733, 17314511, 18498745, 21572988, 24362026, 27705803, 33961781
GO:0005737 Component Cytoplasm IDA 17205132, 18498745
GO:0005737 Component Cytoplasm IEA
GO:0005794 Component Golgi apparatus IDA 21572988
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609073 13597 ENSG00000174989
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N3Y1
Protein name F-box/WD repeat-containing protein 8 (F-box and WD-40 domain-containing protein 8) (F-box only protein 29)
Protein function Substrate-recognition component of the Cul7-RING(FBXW8) ubiquitin ligase complex, which mediates the ubiquitination and subsequent proteasomal degradation of target proteins (PubMed:17205132, PubMed:18498745, PubMed:21572988, PubMed:24362026, Pu
PDB 7Z8B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00646 F-box 117 161 F-box domain Domain
Sequence
MDDYSLDEFRRRWQEELAQAQAPKKRRRPEAAERRARRPEVGSGRGEQASGDPALAQRLL
EGAGRPPAARATRAEGQDVASRSRSPLAREGAGGGEQLVDQLIRDLNEMNDVPFFDIQLP
YELAINIFQYLDRKELGRCAQVSKTWKVIAEDEVLWYRLCQ
QEGHLPDSSISDYSCWKLI
FQECRAKEHMLRTNWKNRKGAVSELEHVPDTVLCDVHSHDGVVIAGYTSGDVRVWDTRTW
DYVAPFLESEDEEDEPGMQPNVSFVRINSSLAVAAYEDGFLNIWDLRTGKYPVHRFEHDA
RIQALALSQDDATVATASAFDVVMLSPNEEGYWQIAAEFEVPKLVQYLEIVPETRRYPVA
VAAAGDLMYLLKAEDSARTLLYAHGPPVTCLDVSANQVAFGVQGLGWVYEGSKILVYSLE
AGRRLLKLGNVLRDFTCVNLSDSPPNLMVSGNMDGRVRIHDLRSGNIALSLSAHQLRVSA
VQMDDWKIVSGGEEGLVSVWDYRMNQKLWEVYSGHPVQHISFSSHSLITANVPYQTVMRN
ADLDSFTTHRRHRGLIRAYEFAVDQLAFQSPLPVCRSSCDAMATHYYDLALAFPYNHV
Sequence length 598
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Ubiquitin mediated proteolysis   Neddylation
Antigen processing: Ubiquitination & Proteasome degradation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs147289806 RCV005910454
Familial cancer of breast Benign rs147289806 RCV005910453
Lung cancer Uncertain significance rs139880165 RCV005926933
Sarcoma Uncertain significance rs139880165 RCV005926931
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Cognition Disorders Associate 22504421
Dementia Associate 22504421
Pancreatic Neoplasms Associate 24362026