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ProteomicsEndosomal chloride/proton exchangers need inhibitory TMEM9 β-subunits for regulation and prevention of disease-causing overactivity
Multi-epitope affinity purification mass spectrometry (meAP-MS) analysis of TMEM9-, TMEM9B- and CLC3- associated proteins from solubilized mouse brain membranes identified chloride channel subtypes CLCN3, 4 and 5 as exclusive interaction partners of TMEM9 and TMM9B.
ORGANISM(S): Mus musculus (Mouse) 
2025-05-07 | PXD061285 | Pride
Ap-ms Chloride channels Membrane protein complex Auxiliary subunits Mouse brain Protein-protein interactions 
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Not available
S-EPMC7820737 | biostudies-literature
UnknownImpaired Autophagic Clearance with a Gain-of-Function Variant of the Lysosomal Cl-/H+ Exchanger ClC-7.
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S-EPMC10742274 | biostudies-literature
UnknownStructural determinants of M-type KCNQ (Kv7) K+ channel assembly.
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S-EPMC6674134 | biostudies-literature
UnknownMolecular basis of ClC-6 function and its impairment in human disease.
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S-EPMC10575590 | biostudies-literature
UnknownUnique variants in CLCN3, encoding an endosomal anion/proton exchanger, underlie a spectrum of neurodevelopmental disorders.
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S-EPMC8387284 | biostudies-literature
UnknownNeuron-oligodendrocyte potassium shuttling at nodes of Ranvier protects against inflammatory demyelination.
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S-EPMC10065072 | biostudies-literature
UnknownDe novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.
Not available
S-EPMC5794876 | biostudies-literature
UnknownX-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.
Not available
S-EPMC5414091 | biostudies-literature
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