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However, the mechanisms regulating brain zinc homeostasis are poorly understood. We performed secondary analyses of brain MRI GWAS and exome sequencing data from adults in the UK Biobank. Coding ZIP12 polymorphisms in zinc transporter ZIP12 (\n                    <jats:italic>SLC39A12)<\/jats:italic>\n                    were associated with altered brain susceptibility weighted MRI (swMRI).\u00a0Conditional and joint association analyses revealed independent GWAS signals in linkage disequilibrium with 2 missense ZIP12 polymorphisms, rs10764176 and\u00a0rs72778328, with reduced zinc transport activity.\u00a0ZIP12 rare coding variants predicted to be deleterious were associated with similar impacts on brain swMRI. In Neuro\u20102a cells, ZIP12 deficiency by short hairpin RNA (shRNA) depletion or CRISPR\/Cas9 genome editing resulted in impaired mitochondrial function, increased superoxide presence, and detectable protein carbonylation.\u00a0Inhibition of Complexes I and IV of the electron transport chain reduced neurite outgrowth in ZIP12 deficient cells.\u00a0Transcriptional coactivator PGC\u20101\u03b1, mitochondrial superoxide dismutase (SOD2), and chemical antioxidants \u03b1\u2010tocopherol, MitoTEMPO, and MitoQ restored neurite extension impaired by ZIP12 deficiency. Mutant forms of \u03b1\u2010synuclein and tau linked to familial Parkinson\u2019s disease and frontotemporal dementia, respectively, reduced neurite outgrowth in cells deficient in ZIP12.\u00a0Zinc and ZIP12 may confer resilience against neurological diseases or premature aging of the brain.\n                  <\/jats:p>","DOI":"10.1096\/fj.202000772r","type":"journal-article","created":{"date-parts":[[2020,7,27]],"date-time":"2020-07-27T09:34:39Z","timestamp":1595842479000},"page":"10702-12725","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":12,"title":["Role of zinc transporter ZIP12 in susceptibility\u2010weighted brain magnetic resonance imaging (MRI) phenotypes and mitochondrial function"],"prefix":"10.1096","volume":"34","author":[{"given":"Morgan D.","family":"Strong","sequence":"first","affiliation":[{"name":"Department of Nutritional Sciences Oklahoma State University Stillwater OK 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