Log in to bookmark this gene

Bookmark This Gene

Gene Gene information from NCBI Gene database.
Entrez ID 157574
Gene name F-box protein 16
Gene symbol FBXO16
Synonyms (NCBI Gene)
FBX16
Chromosome 8
Chromosome location 8p21.1
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.
11 Show/Hide all (11)
miRTarBase ID miRNA Experiments Reference
MIRT991292 hsa-miR-1266 CLIP-seq
MIRT991293 hsa-miR-143 CLIP-seq
MIRT991294 hsa-miR-4518 CLIP-seq
MIRT991295 hsa-miR-4716-3p CLIP-seq
MIRT991296 hsa-miR-4723-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608519 13618 ENSG00000214050
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IX29
Protein name F-box only protein 16
Protein function Probably recognizes and binds to some phosphorylated proteins and promotes their ubiquitination and degradation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12937 F-box-like 89 → 135 F-box-like Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in heart, spleen and colon. {ECO:0000269|PubMed:12243353}.
Sequence
MMAFAPPKNTDGPKMQTKMSTWTPLNHQLLNDRVFEERRALLGKWFDKWTDSQRRRILTG
LLERCSLSQQKFCCRKLQEKIPAEALDFTTKLPRVLSLYIFSFLDPRSLCRCAQVCWHWK
NLAELDQLWMLKCLR
FNWYINFSPTPFEQGIWKKHYIQMVKELHITKPKTPPKDGFVIAD
VQLVTSNSPEEKQSPLSAFRSSSSLRKKNNSGEKALPPWRSSDKHPTDIIRFNYLDNRDP
METVQQGRRKRNQMTPDFSRQSHDKKNKLQDRTRLRKAQSMMSRRNPFPLCP
Sequence length 292
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
Nonpapillary renal cell carcinoma Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (6)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Neoplasms Breast neoplasm Pubtator 30714168 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma BEFREE 30530053
★★★★★
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 30530053
★★★★★
★☆☆☆☆
Found in Text Mining only
Heart Failure Heart failure Pubtator 36656640 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 30714168
★★★★★
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 30530053, 30714168
★★★★★
★☆☆☆☆
Found in Text Mining only