FBXW5 F-box and WD repeat domain containing 5

Information
Symbol
FBXW5
Type
protein-coding
Description
F-box and WD repeat domain containing 5
Entrez Gene ID
54461
Genome
hg19
Position
chr9:139,834,887-139,839,190
Genome
hg38
Position
chr9:136,940,435-136,944,738
MIM
609072 OMIM
HGNC
HGNC:13613 HGNC
Ensembl
ENSG00000159069 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 10
Uncertain significance 0 138
Ranking
ClinVar
0
0
0
154
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 Fbw5
MIM 609072 OMIM
HGNC HGNC:13613 HGNC
Ensembl ENSG00000159069 Ensembl
AllianceGenome HGNC:13613
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000325285.8 hg38 chr9 136,940,435 136,944,738 4,304
ENST00000325285.8 hg19 chr9 139,834,887 139,839,190 4,304
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