NOL11 nucleolar protein 11

Information
Symbol
NOL11
Type
protein-coding
Description
nucleolar protein 11
Entrez Gene ID
25926
Genome
hg19
Position
chr17:65,714,052-65,740,647
Genome
hg38
Position
chr17:67,717,936-67,744,531
MIM
615366 OMIM
HGNC
HGNC:24557 HGNC
Ensembl
ENSG00000130935 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 76
Ranking
ClinVar
0
0
0
84
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
MIM 615366 OMIM
HGNC HGNC:24557 HGNC
Ensembl ENSG00000130935 Ensembl
AllianceGenome HGNC:24557
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000253247.9 hg38 chr17 67,717,936 67,744,531 26,596
ENST00000253247.9 hg19 chr17 65,714,052 65,740,647 26,596
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