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Accordingly, pathogenic variants in deubiquitinating enzymes (DUBs) have been implicated in neurodevelopmental disorders and congenital abnormalities. ATXN7L3 is a component of the DUB module of the Spt-Ada-Gcn5 acetyltransferase (SAGA) complex and two other related DUB modules, and it serves as an obligate adaptor protein of three ubiquitin-specific proteases (USP22, USP27X or USP51).<\/jats:p>\n               <jats:p>Through exome sequencing and by using GeneMatcher, we identified nine individuals with heterozygous variants in ATXN7L3. The core phenotype included global motor and language developmental delay, hypotonia and distinctive facial characteristics, including hypertelorism, epicanthal folds, blepharoptosis, a small nose and mouth, and low-set, posteriorly rotated ears.<\/jats:p>\n               <jats:p>To assess pathogenicity, we investigated the effects of a recurrent nonsense variant [c.340C&amp;gt;T; p.(Arg114Ter)] in fibroblasts of an affected individual. ATXN7L3 protein levels were reduced, and deubiquitylation was impaired, as indicated by an increase in histone H2Bub1 levels.<\/jats:p>\n               <jats:p>This is consistent with the previous observation of increased H2Bub1 levels in Atxn7l3-null mouse embryos, which have developmental delay and embryonic lethality. In conclusion, we present clinical information and biochemical characterization supporting ATXN7L3 variants in the pathogenesis of a rare syndromic neurodevelopmental disorder.<\/jats:p>","DOI":"10.1093\/brain\/awae160","type":"journal-article","created":{"date-parts":[[2024,5,16]],"date-time":"2024-05-16T15:00:48Z","timestamp":1715871648000},"page":"2732-2744","source":"Crossref","is-referenced-by-count":4,"title":["<i>De novo<\/i> variants in <i>ATXN7L3<\/i> lead to developmental delay, hypotonia and distinctive facial features"],"prefix":"10.1093","volume":"147","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3595-7075","authenticated-orcid":false,"given":"Tamar","family":"Harel","sequence":"first","affiliation":[{"name":"Department of Genetics, Hadassah Medical Center , Jerusalem , Israel , 9112001"},{"name":"Faculty of Medicine, Hebrew University of Jerusalem , Jerusalem , Israel , 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