NPIPB11 nuclear pore complex interacting protein family member B11

Information
Symbol
NPIPB11
Type
protein-coding
Description
nuclear pore complex interacting protein family member B11
Entrez Gene ID
728888
Genome
hg19
Position
chr16:29,392,631-29,418,032
Genome
hg38
Position
chr16:29,381,310-29,406,711
HGNC
HGNC:37453 HGNC
Ensembl
ENSG00000254206 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 1 0
Ranking
ClinVar
0
0
0
6
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
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 NPIP
HGNC HGNC:37453 HGNC
Ensembl ENSG00000254206 Ensembl
AllianceGenome HGNC:37453
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000614927.1 hg38 chr16 29,385,034 29,397,696 12,663
ENST00000698511.1 hg38 chr16 29,381,310 29,406,711 25,402
ENST00000524087.5 hg38 chr16 29,381,354 29,404,029 22,676
ENST00000698511.1 hg19 chr16 29,392,631 29,418,032 25,402
ENST00000524087.5 hg19 chr16 29,392,675 29,415,350 22,676
ENST00000614927.1 hg19 chr16 29,396,355 29,409,017 12,663
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