Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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146330 |
Gene nameGene Name - the full gene name approved by the HGNC.
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F-box and leucine rich repeat protein 16 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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FBXL16 |
SynonymsGene synonyms aliases
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C16orf22, Fbl16, c380A1.1 |
ChromosomeChromosome number
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16 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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16p13.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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Members of the F-box protein family, such as FBXL16, are characterized by an approximately 40-amino acid F-box motif. SCF complexes, formed by SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), and F-box proteins, act as protein-ubiquitin ligases. F-box pr |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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GO ID |
Ontology |
Definition |
Evidence |
Reference |
GO:0000209 |
Process |
Protein polyubiquitination |
TAS |
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GO:0005829 |
Component |
Cytosol |
TAS |
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GO:0019005 |
Component |
SCF ubiquitin ligase complex |
IBA |
21873635 |
GO:0031146 |
Process |
SCF-dependent proteasomal ubiquitin-dependent protein catabolic process |
IBA |
21873635 |
GO:0043687 |
Process |
Post-translational protein modification |
TAS |
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q8N461 |
Protein name |
F-box/LRR-repeat protein 16 (F-box and leucine-rich repeat protein 16) |
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 |
PF13516 |
LRR_6 |
318 → 342 |
Leucine Rich repeat |
Repeat |
PF13516 |
LRR_6 |
344 → 368 |
Leucine Rich repeat |
Repeat |
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Sequence |
MSSPGIDGDPKPPCLPRNGLVKLPGQPNGLGAASITKGTPATKNRPCQPPPPPTLPPPSL AAPLSRAALAGGPCTPAGGPASALAPGHPAERPPLATDEKILNGLFWYFSACEKCVLAQV CKAWRRVLYQPKFWAGLTPVLHAKELYNVLPGGEKEFVNLQGFAARGFEGFCLVGVSDLD ICEFIDNYALSKKGVKAMSLKRSTITDAGLEVMLEQMQGVVRLELSGCNDFTEAGLWSSL SARITSLSVSDCINVADDAIAAISQLLPNLAELSLQAYHVTDTALAYFTARQGHSTHTLR LLSCWEITNHGVVNVVHSLPNLTALSLSGCSKVTDDGVELVAENLRKLRSLDLSWCPRIT DMALEYVACDLHRLEELVLDRCVRITDTGLSYLSTMSSLRSLYLRWCCQVQDFGLKHLLA LGSLRLLSLAGCPLLTTTGLSGLVQLQELEELELTNCPGATPELFKYFSQHLPRCLVIE
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Sequence length |
479 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Attention deficit hyperactivity disorder |
Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
29325848 |
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