FBXL8 F-box and leucine rich repeat protein 8

Information
Symbol
FBXL8
Type
protein-coding
Description
F-box and leucine rich repeat protein 8
Entrez Gene ID
55336
Genome
hg19
Position
chr16:67,193,860-67,198,077
Genome
hg38
Position
chr16:67,159,957-67,164,174
MIM
609077 OMIM
HGNC
HGNC:17875 HGNC
Ensembl
ENSG00000135722 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 12
Likely benign 0 8
Uncertain significance 0 52
Ranking
ClinVar
0
0
2
70
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM FBL8
MIM 609077 OMIM
HGNC HGNC:17875 HGNC
Ensembl ENSG00000135722 Ensembl
AllianceGenome HGNC:17875
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000258200.8 hg38 chr16 67,159,957 67,164,174 4,218
ENST00000518148.1 hg38 chr16 67,159,932 67,162,663 2,732
ENST00000521920.5 hg38 chr16 67,160,005 67,162,954 2,950
ENST00000519917.5 hg38 chr16 67,159,961 67,164,174 4,214
ENST00000518148.1 hg19 chr16 67,193,835 67,196,566 2,732
ENST00000258200.8 hg19 chr16 67,193,860 67,198,077 4,218
ENST00000519917.5 hg19 chr16 67,193,864 67,198,077 4,214
ENST00000521920.5 hg19 chr16 67,193,908 67,196,857 2,950
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