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KLHL31;jsessionid=66B9E2E761DC1BA2242A4480EFB3E127
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle
Heart
Jejunum
Heart atrium
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Most Correlated Diseases
Delayed hypersensitivity disorder
Rheumatoid arthritis
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Alpha-1-antitrypsin deficiency
Steinert myotonic dystrophy syndrome
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Levamisole
nateglinide
famciclovir
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lomefloxacin
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Dppa2
PAPOLG
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YBX3
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Literature
Most Relevant Literature
Genomic and Transcriptional Profiles of Kelch-like (klhl) Gene Family in Polyploid Carassius Complex…
Epigenetics of Muscle- and Brain-Specific Expression of KLHL Family Genes.
Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice.
Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis.
Targeting kelch-like (KLHL) proteins: achievements, challenges and perspectives.
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There were no clinical trials for KLHL31;jsessionid=66B9E2E761DC1BA2242A4480EFB3E127
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