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XM_001136067
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Summary
General Info
Body Atlas
Most Correlated Tissues
Liver
Fetal liver
Fetal lung
Stomach fundus
Kidney
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Disease Atlas
Most Correlated Diseases
Gastrointestinal hemorrhage
Complement deficiency disease
Blood coagulation disorder
Amyloidosis
Body mass index
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Pharmaco Atlas
Most Correlated Compounds
Trichloroepoxypropane
Polysaccharides
beta-cyclodextrin-benzaldehyde
n-butoxy-2-propanol
arsenate
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Knockdown Atlas
Most Correlated Gene Perturbations
OGFOD1
NR4A3
TOP1
MYF5
MIR20B
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Curated Studies
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Literature
Most Relevant Literature
Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the F…
FGA Controls VEGFA Secretion to Promote Angiogenesis by Activating the VEGFR2-FAK Signalling Pathway…
A Novel Frameshift Mutation in the FGA Gene (c.196 delT) Leading to Congenital Afibrinogenemia.
Afibrinogenemia with two compound heterozygous mutations in FGA gene.
Serum Proteomic Analysis Identifies SAA1, FGA, SAP, and CETP as New Biomarkers for Eosinophilic Gran…
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Clinical Trials
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