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CNOT1;jsessionid=276F20D88AF8FD17245D282196873C80
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Testis seminiferous tubule
Testes
Ciliary ganglion
Atrioventricular node
Superior cervical ganglion
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Disease Atlas
Most Correlated Diseases
Holoprosencephaly sequence
Pyloric ulcer
Bacterial sepsis of newborn
Mental retardation
Developmental mental disorder
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Most Correlated Compounds
Agouti Signaling Protein
repaglinide
trabectedin
Diazinon
Desoxycorticosterone
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Knockdown Atlas
Most Correlated Gene Perturbations
Alu
robo
MEN1
CASP10
GSDME
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Vissers-Bodmer syndrome caused by a novel de novo CNOT1 frameshift variant.
Fetal Description of the Pancreatic Agenesis and Holoprosencephaly Syndrome Associated to a Specific…
Pathogenicity analysis and splicing rescue of a classical splice site variant (c.1343+1G>T) of CNOT1…
CNOT1 regulates circadian behaviour through Per2 mRNA decay in a deadenylation-dependent manner.
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for CNOT1;jsessionid=276F20D88AF8FD17245D282196873C80
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