All individuals with variants in gene SOX2

25 entries on 1 page. Showing entries 1 - 25.
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00050431 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? bilateral microphthalmos, iris coloboma, microcephaly, absent septum pellucidum, dysplastic corpus callosum, intellectual disability mild, epicanthus, brachycephaly 1 1 Johan den Dunnen
00050673 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected father/child M - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, iris coloboma, autism 1 2 Johan den Dunnen
00154951 - - - F - (Germany) - - - - - ? Global developmental delay (HP:0001263); Microcephaly (HP:0000252); Coloboma (HP:0000589); Dystonia (HP:0001332) 1 1 IMGAG
00377807 - PubMed: Gonzalez Rodriguez 2010 - - - Mexico Mexican-mestizo - - - - retinal disease Bilateral anophthalmia Corpus callosum partial agenesis, ventricular brain dilatation 1 1 LOVD
00449761 - - - M - - (not applicable) white - - - - microcephaly HP:0000528, HP:0002032 1 1 Marketa Wayhelova
00468531 Pat1 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected parents F - France - - - - - MCOP anophthalmia; MRI brain corpus callosum agenesis, Vermian hypoplasia; intellectual disability; short stature 1 1 Johan den Dunnen
00468532 Pat2 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected non-carrier parents M - France - - - - - MCOP 30wg-fetus; microphthalmia, coloboma; MRI brain normal 1 1 Johan den Dunnen
00468533 Pat3 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected parents M - France - - - - - MCOP anophthalmia; MRI brain corpus callosum hypoplasia, periventricular heterotopia; intellectual disability; short stature 1 1 Johan den Dunnen
00468534 Pat4 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - MCOP anophthalmia; MRI brain normal; intellectual disability; growth hormone deficiency; micropenis 1 1 Johan den Dunnen
00468535 Pat5 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected non-carrier parents F - France - - - - - MCOP 30wg-fetus; microphthalmia, athalamia, retinal dysplasia, sclerocornea; MRI brain normal; oesophageal atresia; hemi-uterus 1 1 Johan den Dunnen
00468536 patient;Pat6 PubMed: Menetrey 2002, PubMed: Chassaing 2014 2-generation family, patient and affected fetus (M), unaffected parents F - France - - - - - MCOP anophthalmia; MRI brain normal; oesophageal atresia 1 2 Johan den Dunnen
00468537 Pat7 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected non-carrier parents M - France - - - - - MCOP 28wg-fetus; anophthalmia; MRI brain normal; 1 1 Johan den Dunnen
00468538 Pat8 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected parents M - France - - - - - MCOP anophthalmia, microphthalmia, coloboma; MRI brain corpus callosum hypoplasia; intellectual disability; hypogonadism, micropenis 1 1 Johan den Dunnen
00468539 Pat9 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected non-carrier parents M - France - - - - - MCOP 23wg-fetus; anophthalmia; MRI brain ventriculomegaly; 1 1 Johan den Dunnen
00468540 Pat10 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected non-carrier parents M - France - - - - - MCOP 24wg-fetus; microphthalmia, retinal dysplasia; MRI brain normal; 1 1 Johan den Dunnen
00468541 Pat11 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected parents F - France - - - - - MCOP microphthalmia; intellectual disability; hypogonadism 1 1 Johan den Dunnen
00468542 Pat12 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - MCOP anophthalmia; intellectual disability; growth hormone deficiency; cleft palate 1 1 Johan den Dunnen
00468543 Pat13 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents F - France - - - - - MCOP anophthalmia; MRI brain normal; intellectual disability; atrial septal defect; pyelic dilatation 1 1 Johan den Dunnen
00468544 Pat14 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - MCOP anophthalmia; MRI brain left cerebellar hemisphere hypoplasia; intellectual disability; cryptorchidism 1 1 Johan den Dunnen
00468545 Pat15 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - MCOP anophthalmia, microphthalmia; MRI brain corpus callosum hypoplasia; intellectual disability; oesophageal stenosis; micropenis 1 1 Johan den Dunnen
00468546 Pat16 PubMed: Chassaing 2014 2-generation family, affected fetus, unaffected parents M - France - - - - - MCOP 23wg-fetus; anophthalmia; MRI brain normal; bilateral cleft l/p 1 1 Johan den Dunnen
00468547 Pat17 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents F - France - - - - - MCOP anophthalmia; MRI brain corpus callosum hypoplasia, Vermian hypoplasia; intellectual disability; growth hormone deficiency; hypogonadism 1 1 Johan den Dunnen
00468548 Pat18 PubMed: Chassaing 2014 2-generation family, 1 affected, unaffected non-carrier parents F - France - - - - - MCOP anophthalmia, microphthalmia; MRI brain normal; intellectual disability; growth hormone deficiency; hypogonadism 1 1 Johan den Dunnen
00469411 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00472393 361390 - - F ? Syria - - - - - MCOPS3 Microcephaly, Anophthalmia, Abnormal optic chiasm morphology, Optic nerve aplasia 1 1 Andreas Laner
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