NAP1L4 nucleosome assembly protein 1 like 4

Information
Symbol
NAP1L4
Type
protein-coding
Description
nucleosome assembly protein 1 like 4
Entrez Gene ID
4676
Genome
hg19
Position
chr11:2,965,661-3,013,607
Genome
hg38
Position
chr11:2,944,431-2,992,377
MIM
601651 OMIM
HGNC
HGNC:7640 HGNC
Ensembl
ENSG00000205531 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
50
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
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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 NAP1L4b
SYNONYM NAP2
SYNONYM NAP2L
SYNONYM hNAP2
MIM 601651 OMIM
HGNC HGNC:7640 HGNC
Ensembl ENSG00000205531 Ensembl
AllianceGenome HGNC:7640
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380542.9 hg38 chr11 2,944,437 2,992,329 47,893
ENST00000703798.1 hg38 chr11 2,944,437 2,992,292 47,856
ENST00000526115.5 hg38 chr11 2,945,112 2,992,377 47,266
ENST00000448187.6 hg38 chr11 2,944,444 2,992,300 47,857
ENST00000620138.4 hg38 chr11 2,944,431 2,992,377 47,947
ENST00000380542.9 hg19 chr11 2,965,667 3,013,559 47,893
ENST00000448187.6 hg19 chr11 2,965,674 3,013,530 47,857
ENST00000526115.5 hg19 chr11 2,966,342 3,013,607 47,266
ENST00000620138.4 hg19 chr11 2,965,661 3,013,607 47,947
ENST00000703798.1 hg19 chr11 2,965,667 3,013,522 47,856
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