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MKS1;jsessionid=284B3775ECBFC3F7278A83CC9A84F216
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Granulocyte-macrophage progenitor cell of bone marrow
Parotid gland
Transverse colon
Skeletal muscle psoas
Bladder
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Disease Atlas
Most Correlated Diseases
Bardet-Biedl syndrome
Placental insufficiency
Myoneural disorder
Pyloric ulcer
Disorder of brain
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Pharmaco Atlas
Most Correlated Compounds
Bethanechol
Acebutolol
Sulfadimethoxine
Hexamethonium
Methionine Sulfoximine
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Knockdown Atlas
Most Correlated Gene Perturbations
RPL35
YAF2
ZNF131
RARA
STAB1
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Regulation of canonical Wnt signalling by the ciliopathy protein MKS1 and the E2 ubiquitin-conjugati…
Case Report: Preimplantation Genetic Testing for Meckel Syndrome Induced by Novel Compound Heterozyg…
Formation of the B9-domain protein complex MKS1-B9D2-B9D1 is essential as a diffusion barrier for ci…
Mitochondrial Retrograde Signaling Contributes to Metabolic Differentiation in Yeast Colonies.
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for MKS1;jsessionid=284B3775ECBFC3F7278A83CC9A84F216
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