{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,9]],"date-time":"2026-05-09T07:31:25Z","timestamp":1778311885828,"version":"3.51.4"},"reference-count":11,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2014,10,30]],"date-time":"2014-10-30T00:00:00Z","timestamp":1414627200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Genetics"],"published-print":{"date-parts":[[2015,9]]},"abstract":"The aim of this study is to investigate the genetic basis of autosomal recessive congenital cataract and intellectual disability phenotype in a consanguineous Tunisian family. The whole genome scan of the studied family was performed with single nucleotide polymorphisms (SNPs<\/jats:styled-content>). The resulted runs of homozygosity (ROH) were analyzed through the integrated Systems Tool for Eye gene discovery (iSyTE) in order to prioritize candidate genes associated with congenital cataract. Selected genes were amplified and sequenced. Bioinformatic analysis was conducted to predict the function of the mutant gene. We identified a new specific lens gene named syntaxin 3<\/jats:italic> linked to the studied phenotype. The direct sequencing of this gene revealed a novel missense mutation c.122A<\/jats:styled-content>>G which results in p.E41G<\/jats:styled-content>. Bioinformatic analysis suggested a deleterious effect of this mutation on protein structure and function. Here, we report for the first time a missense mutation of a novel lens specific gene STX3<\/jats:styled-content><\/jats:italic> in a phenotype associating autosomal recessive congenital cataract and intellectual disability.<\/jats:p>","DOI":"10.1111\/cge.12489","type":"journal-article","created":{"date-parts":[[2014,10,31]],"date-time":"2014-10-31T02:12:48Z","timestamp":1414721568000},"page":"283-287","source":"Crossref","is-referenced-by-count":13,"title":["Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3<\/scp><\/i> in a consanguineous Tunisian family"],"prefix":"10.1111","volume":"88","author":[{"given":"M.","family":"Chograni","sequence":"first","affiliation":[{"name":"Laboratory of Human Genetics, Faculty of Medicine of Tunis University Tunis ElManar Tunis Tunisia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.S.","family":"Alkuraya","sequence":"additional","affiliation":[{"name":"Developmental Genetics Unit King Faisal Specialist Hospital and Research Center Riyad Saudi Arabia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Ourteni","sequence":"additional","affiliation":[{"name":"Congenital and Hereditary Disorders Department Charles Nicolle hospital Tunis Tunisia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"F.","family":"Maazoul","sequence":"additional","affiliation":[{"name":"Congenital and Hereditary Disorders Department Charles Nicolle hospital Tunis Tunisia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Lariani","sequence":"additional","affiliation":[{"name":"Laboratory of Human Genetics, Faculty of Medicine of Tunis University Tunis ElManar Tunis Tunisia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.B.","family":"Chaabouni","sequence":"additional","affiliation":[{"name":"Laboratory of Human Genetics, Faculty of Medicine of Tunis University Tunis ElManar Tunis Tunisia"},{"name":"Congenital and Hereditary Disorders Department Charles Nicolle hospital Tunis Tunisia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2014,10,30]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/S1350-9462(98)00018-4"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1007\/s004390051002"},{"key":"e_1_2_6_4_1","first-page":"2007","article-title":"Cat\u2010Map: putting cataract on the map","volume":"16","author":"Shiels A","year":"2010","journal-title":"Mol Vis"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1167\/iovs.11-8839"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1093\/bioinformatics\/18.9.1250"},{"key":"e_1_2_6_7_1","doi-asserted-by":"publisher","DOI":"10.1093\/nar\/gkg520"},{"key":"e_1_2_6_8_1","doi-asserted-by":"publisher","DOI":"10.1186\/1471-2415-11-35"},{"key":"e_1_2_6_9_1","doi-asserted-by":"publisher","DOI":"10.4236\/ojoph.2012.23014"},{"key":"e_1_2_6_10_1","doi-asserted-by":"publisher","DOI":"10.1006\/bbrc.1995.1910"},{"key":"e_1_2_6_11_1","doi-asserted-by":"publisher","DOI":"10.1083\/jcb.201310134"},{"key":"e_1_2_6_12_1","doi-asserted-by":"publisher","DOI":"10.1523\/JNEUROSCI.16-21-06713.1996"}],"container-title":["Clinical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fcge.12489","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1111\/cge.12489","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,10,3]],"date-time":"2023-10-03T11:58:00Z","timestamp":1696334280000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1111\/cge.12489"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,10,30]]},"references-count":11,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2015,9]]}},"alternative-id":["10.1111\/cge.12489"],"URL":"https:\/\/doi.org\/10.1111\/cge.12489","archive":["Portico"],"relation":{},"ISSN":["0009-9163","1399-0004"],"issn-type":[{"value":"0009-9163","type":"print"},{"value":"1399-0004","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,10,30]]}}}