FBXO7 F-box protein 7

Information
Symbol
FBXO7
Type
protein-coding
Description
F-box protein 7
Entrez Gene ID
25793
Genome
hg19
Position
chr22:32,870,798-32,894,816
Genome
hg38
Position
chr22:32,474,811-32,498,829
MIM
605648 OMIM
HGNC
HGNC:13586 HGNC
Ensembl
ENSG00000100225 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 64
Likely pathogenic 0 16
Benign 0 68
Likely benign 0 402
Conflicting classifications of pathogenicity 0 18
Uncertain significance 0 212
Ranking
ClinVar
0
0
68
682
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
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 FBX
SYNONYM FBX07
SYNONYM FBX7
SYNONYM PARK15
SYNONYM PKPS
MIM 605648 OMIM
HGNC HGNC:13586 HGNC
Ensembl ENSG00000100225 Ensembl
AllianceGenome HGNC:13586
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000266087.12 hg38 chr22 32,474,811 32,498,829 24,019
ENST00000452138.3 hg38 chr22 32,475,237 32,498,608 23,372
ENST00000397426.5 hg38 chr22 32,475,257 32,498,829 23,573
ENST00000266087.12 hg19 chr22 32,870,798 32,894,816 24,019
ENST00000452138.3 hg19 chr22 32,871,224 32,894,595 23,372
ENST00000397426.5 hg19 chr22 32,871,244 32,894,816 23,573
Genome browser