TXN2 thioredoxin 2

Information
Symbol
TXN2
Type
protein-coding
Description
thioredoxin 2
Entrez Gene ID
25828
Genome
hg19
Position
chr22:36,863,093-36,877,687
Genome
hg38
Position
chr22:36,467,046-36,481,640
MIM
609063 OMIM
HGNC
HGNC:17772 HGNC
Ensembl
ENSG00000100348 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 12
Likely benign 0 34
Uncertain significance 0 48
Ranking
ClinVar
0
0
14
76
2
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 :
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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 :
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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 COXPD29
SYNONYM MT-TRX
SYNONYM MTRX
SYNONYM TRX2
SYNONYM TXN
MIM 609063 OMIM
HGNC HGNC:17772 HGNC
Ensembl ENSG00000100348 Ensembl
AllianceGenome HGNC:17772
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000416967.1 hg38 chr22 36,467,046 36,481,634 14,589
ENST00000403313.5 hg38 chr22 36,467,591 36,481,340 13,750
ENST00000216185.7 hg38 chr22 36,467,046 36,481,640 14,595
ENST00000416967.1 hg19 chr22 36,863,093 36,877,681 14,589
ENST00000216185.7 hg19 chr22 36,863,093 36,877,687 14,595
ENST00000403313.5 hg19 chr22 36,863,638 36,877,387 13,750
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