STAT2 signal transducer and activator of transcription 2

Information
Symbol
STAT2
Type
protein-coding
Description
signal transducer and activator of transcription 2
Entrez Gene ID
6773
Genome
hg19
Position
chr12:56,735,381-56,753,891
Genome
hg38
Position
chr12:56,341,597-56,360,107
MIM
600556 OMIM
HGNC
HGNC:11363 HGNC
Ensembl
ENSG00000170581 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 52
Likely pathogenic 0 6
Benign 0 30
Likely benign 0 396
Conflicting classifications of pathogenicity 0 12
Likely risk allele 0 2
Uncertain significance 0 404
Ranking
ClinVar
0
0
66
810
10
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 :
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 IMD44
SYNONYM ISGF-3
SYNONYM P113
SYNONYM PTORCH3
SYNONYM STAT113
MIM 600556 OMIM
HGNC HGNC:11363 HGNC
Ensembl ENSG00000170581 Ensembl
AllianceGenome HGNC:11363
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000557235.5 hg38 chr12 56,342,936 56,360,126 17,191
ENST00000698193.1 hg38 chr12 56,342,366 56,360,203 17,838
ENST00000314128.9 hg38 chr12 56,341,597 56,360,107 18,511
ENST00000651915.1 hg38 chr12 56,341,608 56,360,131 18,524
ENST00000698186.1 hg38 chr12 56,341,606 56,360,203 18,598
ENST00000314128.9 hg19 chr12 56,735,381 56,753,891 18,511
ENST00000557235.5 hg19 chr12 56,736,720 56,753,910 17,191
ENST00000698193.1 hg19 chr12 56,736,150 56,753,987 17,838
ENST00000698186.1 hg19 chr12 56,735,390 56,753,987 18,598
ENST00000651915.1 hg19 chr12 56,735,392 56,753,915 18,524
Genome browser