CUL9 cullin 9

Information
Symbol
CUL9
Type
protein-coding
Description
cullin 9
Entrez Gene ID
23113
Genome
hg19
Position
chr6:43,149,934-43,192,325
Genome
hg38
Position
chr6:43,182,196-43,224,587
MIM
607489 OMIM
HGNC
HGNC:15982 HGNC
Ensembl
ENSG00000112659 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 52
Likely benign 0 88
Conflicting classifications of pathogenicity 0 4
Uncertain significance 0 304
Ranking
ClinVar
0
0
12
422
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 :
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 H7AP1
SYNONYM PARC
MIM 607489 OMIM
HGNC HGNC:15982 HGNC
Ensembl ENSG00000112659 Ensembl
AllianceGenome HGNC:15982
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000252050.9 hg38 chr6 43,182,196 43,224,587 42,392
ENST00000372647.6 hg38 chr6 43,182,185 43,224,585 42,401
ENST00000372647.6 hg19 chr6 43,149,923 43,192,323 42,401
ENST00000252050.9 hg19 chr6 43,149,934 43,192,325 42,392
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