NOP58 NOP58 ribonucleoprotein

Information
Symbol
NOP58
Type
protein-coding
Description
NOP58 ribonucleoprotein
Entrez Gene ID
51602
Genome
hg19
Position
chr2:203,130,486-203,168,384
Genome
hg38
Position
chr2:202,265,763-202,303,661
MIM
616742 OMIM
HGNC
HGNC:29926 HGNC
Ensembl
ENSG00000055044 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
30
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 HSPC120
SYNONYM NOP5
SYNONYM NOP5/NOP58
MIM 616742 OMIM
HGNC HGNC:29926 HGNC
Ensembl ENSG00000055044 Ensembl
AllianceGenome HGNC:29926
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000264279.10 hg38 chr2 202,265,763 202,303,661 37,899
ENST00000264279.10 hg19 chr2 203,130,486 203,168,384 37,899
KeyValue
strand+
start203,130,438
Gene SymbolNOP58
Entrez GeneId51,602
Chr Band2q33.1
end203,168,383
chrchr2
Genome browser