FBXW9 F-box and WD repeat domain containing 9

Information
Symbol
FBXW9
Type
protein-coding
Description
F-box and WD repeat domain containing 9
Entrez Gene ID
84261
Genome
hg19
Position
chr19:12,799,730-12,807,445
Genome
hg38
Position
chr19:12,688,916-12,696,631
MIM
609074 OMIM
HGNC
HGNC:28136 HGNC
Ensembl
ENSG00000132004 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
72
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 :
Search word :
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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 Fbw9
SYNONYM MEC-15
MIM 609074 OMIM
HGNC HGNC:28136 HGNC
Ensembl ENSG00000132004 Ensembl
AllianceGenome HGNC:28136
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393261.8 hg38 chr19 12,688,916 12,696,631 7,716
ENST00000587955.1 hg38 chr19 12,689,216 12,696,581 7,366
ENST00000393261.8 hg19 chr19 12,799,730 12,807,445 7,716
ENST00000587955.1 hg19 chr19 12,800,030 12,807,395 7,366
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