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Med13L
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Dendritic (plasmacytoid) cell
Basophil of peripheral blood
Saphenous vein
Myometrium
Nipple cross-section
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Disease Atlas
Most Correlated Diseases
Chronic fatigue syndrome
Disorder of pregnancy
Congenital heart disease
Helicobacter pylori gastrointestinal tract infection
Congenital glucose-galactose malabsorption
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Most Correlated Compounds
Tolnaftate
Mesalamine
hydroxyachillin
Cefotetan
Propidium
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Most Correlated Gene Perturbations
FGFR1
H2-Eb2
HLA-DQA1
ASTN1
CCDC170
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
Molecular and Functional Characterisation of a Novel Intragenic 12q24.21 Deletion Resulting in MED13…
Performance of meta-predictors for the classification of MED13L missense variations, implication of …
MED13L and its disease-associated variants influence the dendritic development of cerebral cortical …
Two novel pathogenic variants in MED13L: one familial and one isolated case.
MED13L-related intellectual disability due to paternal germinal mosaicism.
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Clinical Trials
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Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight
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