NUFIP2 nuclear FMR1 interacting protein 2

Information
Symbol
NUFIP2
Type
protein-coding
Description
nuclear FMR1 interacting protein 2
Entrez Gene ID
57532
Genome
hg19
Position
chr17:27,582,857-27,621,166
Genome
hg38
Position
chr17:29,255,839-29,294,148
MIM
609356 OMIM
HGNC
HGNC:17634 HGNC
Ensembl
ENSG00000108256 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 28
Uncertain significance 0 56
Ranking
ClinVar
0
0
0
94
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 :
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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 182-FIP
SYNONYM 82-FIP
SYNONYM FIP-82
SYNONYM NUFP2
SYNONYM PIG1
MIM 609356 OMIM
HGNC HGNC:17634 HGNC
Ensembl ENSG00000108256 Ensembl
AllianceGenome HGNC:17634
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000579665.1 hg38 chr17 29,264,399 29,294,115 29,717
ENST00000225388.9 hg38 chr17 29,255,839 29,294,148 38,310
ENST00000225388.9 hg19 chr17 27,582,857 27,621,166 38,310
ENST00000579665.1 hg19 chr17 27,591,417 27,621,133 29,717
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