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Clcn7
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Summary
General Info
Body Atlas
Most Correlated Tissues
Skeletal muscle psoas
Atrioventricular node
Superior cervical ganglion
Ciliary ganglion
Globus pallidus
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Disease Atlas
Most Correlated Diseases
Osteopetrosis
Infantile malignant osteopetrosis
Methicillin resistant Staphylococcus aureus infection
Disease caused by rickettsiae
Cryptosporidiosis
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Pharmaco Atlas
Most Correlated Compounds
Minocycline
ginkgolide A
Tetracaine
5-chloro-1-(4-chlorobenzyl)-3-(phenylthio)indole-2-carboxylic acid
Xylazine
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Knockdown Atlas
Most Correlated Gene Perturbations
Mir181b1
GIMAP5
NR2E1
DUT
Mir9-3
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Curated Studies
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Literature
Most Relevant Literature
CLCN7, a gene shared by autosomal recessive and autosomal dominant osteopetrosis.
The Role of the Lysosomal Cl-/H+ Antiporter ClC-7 in Osteopetrosis and Neurodegeneration.
The chloride antiporter CLCN7 is a modifier of lysosome dysfunction in FIG4 and VAC14 mutants.
H(+)/Cl(‑) exchange transporter 7 promotes lysosomal acidification‑mediated autophagy in mouse cardi…
A Mild Case of Autosomal Recessive Osteopetrosis Masquerading as the Dominant Form Involving Homozyg…
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Clinical Trials
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