NHP2 NHP2 ribonucleoprotein

Information
Symbol
NHP2
Type
protein-coding
Description
NHP2 ribonucleoprotein
Entrez Gene ID
55651
Genome
hg19
Position
chr5:177,576,464-177,580,886
Genome
hg38
Position
chr5:178,149,463-178,153,885
MIM
606470 OMIM
HGNC
HGNC:14377 HGNC
Ensembl
ENSG00000145912 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Benign 0 22
Likely benign 0 136
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 196
Ranking
ClinVar
0
0
42
300
6
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 DKCB2
SYNONYM NHP2P
SYNONYM NOLA2
MIM 606470 OMIM
HGNC HGNC:14377 HGNC
Ensembl ENSG00000145912 Ensembl
AllianceGenome HGNC:14377
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000274606.8 hg38 chr5 178,149,463 178,153,885 4,423
ENST00000314397.9 hg38 chr5 178,149,463 178,153,848 4,386
ENST00000314397.9 hg19 chr5 177,576,464 177,580,849 4,386
ENST00000274606.8 hg19 chr5 177,576,464 177,580,886 4,423
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