NOL12 nucleolar protein 12

Information
Symbol
NOL12
Type
protein-coding
Description
nucleolar protein 12
Entrez Gene ID
79159
Genome
hg19
Position
chr22:38,082,350-38,089,481
Genome
hg38
Position
chr22:37,686,343-37,693,474
HGNC
HGNC:28585 HGNC
Ensembl
ENSG00000273899 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
34
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 Nop25
SYNONYM dJ37E16.7
HGNC HGNC:28585 HGNC
Ensembl ENSG00000273899 Ensembl
AllianceGenome HGNC:28585
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000359114.9 hg38 chr22 37,686,343 37,693,474 7,132
ENST00000611699.1 hg38 chr22 37,686,360 37,693,471 7,112
ENST00000359114.9 hg19 chr22 38,082,350 38,089,481 7,132
ENST00000611699.1 hg19 chr22 38,082,367 38,089,478 7,112
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