Gene Gene information from NCBI Gene database.
Entrez ID 80028
Gene name F-box and leucine rich repeat protein 18
Gene symbol FBXL18
Synonyms (NCBI Gene)
Fbl18
Chromosome 7
Chromosome location 7p22.1
Summary The protein encoded by this gene is a member of a family of proteins that contain an approximately 40-amino acid F-box motif. This motif is important for interaction with SKP1 and for targeting some proteins for degradation. The encoded protein has been s
miRNA miRNA information provided by mirtarbase database.
1408
miRTarBase ID miRNA Experiments Reference
MIRT022552 hsa-miR-124-3p Microarray 18668037
MIRT031644 hsa-miR-16-5p Sequencing 20371350
MIRT042025 hsa-miR-484 CLASH 23622248
MIRT041358 hsa-miR-193b-3p CLASH 23622248
MIRT610164 hsa-miR-8485 HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005829 Component Cytosol TAS
GO:0031146 Process SCF-dependent proteasomal ubiquitin-dependent protein catabolic process IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609084 21874 ENSG00000155034
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96ME1
Protein name F-box/LRR-repeat protein 18 (F-box and leucine-rich repeat protein 18)
Protein function Substrate-recognition component of the SCF (SKP1-CUL1-F-box protein)-type E3 ubiquitin ligase complex.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00646 F-box 27 74 F-box domain Domain
Sequence
MASSGEDISNDDDDMHPAAAGMADGVHLLGFSDEILLHILSHVPSTDLILNVRRTCRKLA
ALCLDKSLIHTVLL
QKDYQASEDKVRQLVKEIGREIQQLSMAGCYWLPGSTVEHVARCRS
LVKVNLSGCHLTSLRLSKMLSALQHLRSLAIDVSPGFDASQLSSECKATLSRVRELKQTL
FTPSYGVVPCCTSLEKLLLYFEILDRTREGAILSGQLMVGQSNVPHYQNLRVFYARLAPG
YINQEVVRLYLAVLSDRTPQNLHAFLISVPGSFAESGATKNLLDSMARNVVLDALQLPKS
WLNGSSLLQHMKFNNPFYFSFSRCTLSGGHLIQQVINGGKDLRSLASLNLSGCVHCLSPD
SLLRKAEDDIDSSILETLVASCCNLRHLNLSAAHHHSSEGLGRHLCQLLARLRHLRSLSL
PVCSVADSAPRADRAPAQPAMHAVPRGFGKKVRVGVQSCPSPFSGQACPQPSSVFWSLLK
NLPFLEHLELIGSNFSSAMPRNEPAIRNSLPPCSRAQSVGDSEVAAIGQLAFLRHLTLAQ
LPSVLTGSGLVNIGLQCQQLRSLSLANLGMMGKVVYMPALSDMLKHCKRLRDLRLEQPYF
SANAQFFQALSQCPSLQRLCLVSRSGTLQPDAVLAFMARCLQVVMCHLFTGESLATCKSL
QQSLLRRWGEVTGRRPQLFTELREEPSARTSRATGRRQPCLPDSGVVCCPCGRPLAVSGI
ILVGVSPSLVVKTTCVYRVLFKNLDYASIFFLVCLFETESHSVVQAGVQWRDLSSLQPLL
SGLQPQPPEQLENELEIGFSYCFVI
Sequence length 805
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Thyroid cancer, nonmedullary, 1 Benign rs74478333 RCV005908441
Uterine carcinosarcoma Benign rs74478333 RCV005908440
Uterine corpus endometrial carcinoma Benign rs74478333 RCV005908442
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Glioma Associate 27926990