chr3:128479427:> Detail (hg38) (GATA2)

Information

Genome

Assembly Position
hg19 chr3:128,198,270-128,212,028 
hg38 chr3:128,479,427-128,493,185

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
lung adenocarcinoma Fasudil,Bortezomib D Predictive Supports Sensitivity/Response Somatic 4 22541434 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
Targeting overactive GATA2-mediated pathways with inhibitors bortezomib and fasudil led to dramatic ... CIViC Evidence Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr3:128,479,427-128,493,185
Variant Type
snv
Variant (CIViC) (CIViC Variant)
EXPRESSION
Transcript 1 (CIViC Variant)
ENST00000341105.2
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/57
Summary (CIViC Variant)
GATA2 misregulation has been observed in a number of hematologic malignancies, as well as non-small cell lung cancer. Treatment of over-active GATA2 pathways using the proteasome inhibitor bortezomib has shown dramatic tumor regression in lung cancer.
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