NOL8 nucleolar protein 8

Information
Symbol
NOL8
Type
protein-coding
Description
nucleolar protein 8
Entrez Gene ID
55035
Genome
hg19
Position
chr9:95,059,772-95,087,632
Genome
hg38
Position
chr9:92,297,490-92,325,350
MIM
611534 OMIM
HGNC
HGNC:23387 HGNC
Ensembl
ENSG00000198000 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 12
Uncertain significance 0 100
Ranking
ClinVar
0
0
0
112
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 C9orf34
SYNONYM NOP132
SYNONYM bA62C3.3
SYNONYM bA62C3.4
MIM 611534 OMIM
HGNC HGNC:23387 HGNC
Ensembl ENSG00000198000 Ensembl
AllianceGenome HGNC:23387
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000545558.5 hg38 chr9 92,297,490 92,325,350 27,861
ENST00000358855.8 hg38 chr9 92,297,359 92,325,594 28,236
ENST00000442668.7 hg38 chr9 92,297,358 92,325,350 27,993
ENST00000535387.5 hg38 chr9 92,297,836 92,324,161 26,326
ENST00000542053.5 hg38 chr9 92,297,836 92,325,333 27,498
ENST00000358855.8 hg19 chr9 95,059,641 95,087,876 28,236
ENST00000442668.7 hg19 chr9 95,059,640 95,087,632 27,993
ENST00000535387.5 hg19 chr9 95,060,118 95,086,443 26,326
ENST00000542053.5 hg19 chr9 95,060,118 95,087,615 27,498
ENST00000545558.5 hg19 chr9 95,059,772 95,087,632 27,861
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