NXN nucleoredoxin

Information
Symbol
NXN
Type
protein-coding
Description
nucleoredoxin
Entrez Gene ID
64359
Genome
hg19
Position
chr17:702,550-883,016
Genome
hg38
Position
chr17:799,310-979,776
MIM
612895 OMIM
HGNC
HGNC:18008 HGNC
Ensembl
ENSG00000167693 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 2
Benign 0 98
Likely benign 0 174
Uncertain significance 0 110
Ranking
ClinVar
0
0
50
332
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 NRX
SYNONYM RRS2
SYNONYM TRG-4
MIM 612895 OMIM
HGNC HGNC:18008 HGNC
Ensembl ENSG00000167693 Ensembl
AllianceGenome HGNC:18008
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000537628.6 hg38 chr17 800,768 864,097 63,330
ENST00000575801.5 hg38 chr17 799,313 864,111 64,799
ENST00000336868.8 hg38 chr17 799,310 979,776 180,467
ENST00000336868.8 hg19 chr17 702,550 883,016 180,467
ENST00000575801.5 hg19 chr17 702,553 767,351 64,799
ENST00000537628.6 hg19 chr17 704,008 767,337 63,330
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