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KLHL31
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NextBio Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle
Heart
Jejunum
Heart atrium
Heart ventricle
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Disease Atlas
Most Correlated Diseases
Delayed hypersensitivity disorder
Rheumatoid arthritis
Alpha-1-antitrypsin deficiency
Disorder of digestive system
Arthropathy
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Most Correlated Compounds
Levamisole
famciclovir
dexamisole
Floxuridine
lomefloxacin
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Most Correlated Gene Perturbations
Dppa2
PAPOLG
PAPOLA
YBX3
ENPP2
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.
Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis.
A novel zebrafish kelchlike gene klhl and its human ortholog KLHL display conserved expression patte…
Klhl31 is associated with skeletal myogenesis and its expression is regulated by myogenic signals an…
A novel human BTB-kelch protein KLHL31, strongly expressed in muscle and heart, inhibits transcripti…
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