Variant Details for FBXL18


Gene Symbol: | FBXL18 ( FLJ10776,FLJ11467,FLJ26934,FLJ38075,FLJ41541,Fbl18 ) |
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Gene Full Name: | F-box and leucine-rich repeat protein 18 |
Band: | 7p22.1 |
Quick Links | Entrez ID:80028; OMIM: 609084; Uniprot ID:FXL18_HUMAN; ENSEMBL ID: ENSG00000155034; HGNC ID: 21874 |
Relate to Another Database: | SFARIGene; denovo-db |


Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. Chromosome coordinates: hg19
Genetic Category | CNVs/SVs | de novo Mutations | Mosaics SNVs | NGS Other Mutations | Low-Scale Gene Mutations | Linkage Regions | Total |
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Number | 4 | 0 | 0 | 0 | 0 | 0 | 4 |


CNV ID | Chr | Band | Start | End | Size | Gain/Loss | UCSC Browser | Reference |
---|---|---|---|---|---|---|---|---|
AutCNV0000249 | 7 | 7p22.2-22.1 | 2133474 | 7233475 | 5100001 | loss | external link | Yu, 2002 |
AutCNV0000730 | 7 | 7p22.1 | 5133474 | 6533475 | 1400001 | gain | external link | Bremer, 2011 |
AutCNV0004828 | 7 | 7p22.1 | gain | Goitia V, 2015 | ||||
AutCNV0005695 | 7 | loss | Yuen RK, 2016 |


iFish (integrated Functional inference of SNVs in human) is based on gene/gene family customized models to classify missense mutations.
Chr | Pos | Ref | Alt | Coding | AA | Validated Method | iFish Prediction | iFish Probability | Reference |
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No related data! |


Chr | Position | Ref | Alt | Genotype | Validated Method | Reference |
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No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
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No related data! |


Chr | Pos | Ref | Alt | Coding | AA | Validated | iFish Prediction | iFish Probability | Reference |
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No related data! |


Linkage Name | Band | Chr | Marker | LOD | NPL | P Value | Reference |
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No related data! |