ATP6V0A2

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ATP6V0A2

A gene on chromosome 12q24.31 that encodes a subunit of H+-ATPase (also known as V-ATPase, vacuolar ATPase), a multisubunit enzyme that mediates acidification of eukaryotic intracellular organelles, which is required for an array of molecular processes, including protein sorting, zymogen activation, receptor-mediated endocytosis and synaptic vesicle proton gradient generation.

Molecular pathology
ATP6V0A2 mutations cause cutis laxa type II and wrinkly skin syndrome.
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As part of Strand 2 of the ARCL project, researchers have been observing IDL lessons and interviewing stakeholders in order to develop a better understanding of how students, teachers, parents/carers and others use the technology, what they feel about their engagement in IDL activities and how those experiences influence their perceptions, satisfaction, behaviours, working practices, learning process and (learning) outcomes.
Tenders are invited for Casual Renewal of Damaged PSC line sleeper, Pulling back , Distressing, Lifting of Track, Providing Gap less joint in CMS Xings, Providing Missing land boundary pillars, Fixing Gang Board/Jurisdiction Board, Protection of unauthorized Track Crossing, Wedening of Cess, Raising of Cess, Slope Repairing, Repairs to Trolley Refuges, Spreading of Track Ballast and other Related track works in between ARCL