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ATP6V1B2
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Neutrophil of bone marrow
Frontal cortex
Substantia nigra pars compacta
Microglial cell
Whole blood
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Disease Atlas
Most Correlated Diseases
Caseating tuberculoid granuloma
Bacterial pneumonia
Chronic fatigue syndrome
Hemorrhagic shock
Disease caused by parasite
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Pharmaco Atlas
Most Correlated Compounds
perfosfamide
Practolol
JM 3100
Ornithogalum glycoside
8-sulfocholecystokinin octapeptide
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Knockdown Atlas
Most Correlated Gene Perturbations
GATA5
PLEKHG6
TBL1X
CYP2C19
HOXC6
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
ATP6V1B2-related epileptic encephalopathy.
DOORS syndrome and a recurrentĀ truncating ATP6V1B2 variant.
Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with hete…
SIRT1 Interacts with and Deacetylates ATP6V1B2 in Mature Adipocytes.
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for ATP6V1B2
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