All individuals with variants in gene PACS1

12 entries on 1 page. Showing entries 1 - 12.
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00050380 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, defect in the atrial septum, inguinal hernia, postnatal microcephaly, progressive microcephaly, slender tapering fingers, hypoplastic male genitalia, hypertelorism, shallow orbits, thin upper lip vermilion, long palpebral fissure, downslanted palpebral fissures, slender long bone, flared iliac wings 1 1 Johan den Dunnen
00050384 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? defect in the atrial septum, seizures, microcephaly, delayed speech and language development, cryptorchidism, global developmental delay 1 1 Johan den Dunnen
00050525 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, delayed speech and language development, low-set ears, anteverted nares, bulbous nose, flat forehead, 2-3 toe syndactyly, joint laxity, cortical dysplasia, abnormality of blood and blood-forming tissues 1 1 Johan den Dunnen
00050682 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? absence seizures, generalized tonic-clonic seizures, seizures, seizures, frontal upsweep of hair, abnormality of the orbital region, downslanted palpebral fissures, long palpebral fissure, thin upper lip vermilion, umbilical hernia, webbed neck, pectus excavatum 1 1 Johan den Dunnen
00092244 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 2-generation family, 1 affected, unaffected non-carrier parents F - United States - - - - - SHMS;MRD17 severe IDD, microcephaly, facial dysmorphisms, myopia, bifid uvula and submucous cleft, dysplastic pulmonary, aortic valves, failure to thrive progressive ataxia and cerebellar atrophy; neurodegeneration progressive cerebellar atrophy 1 1 Johan den Dunnen
00164662 23159249-Pat1 PubMed: Schuurs-Hoeijmakers 2012 2-generation family, 1 affected, unaffected non-carrier parents M no Netherlands - - - - - ID see paper; ..., remarkable face 1 1 Johan den Dunnen
00164663 23159249-Pat2 PubMed: Schuurs-Hoeijmakers 2012 2-generation family, 1 affected, unaffected non-carrier parents M no Belgium - - - - - ID see paper; ..., remarkable face 1 1 Johan den Dunnen
00303029 Pat74 PubMed: Helbig 2016 - - - United States - - - - - seizures Unclassified epilepsy; age onset neonatal 1 1 Johan den Dunnen
00325388 Pat1 PubMed: Hong 2020 - F - Taiwan - - - - - ? 1d-onset seizures; focal seizures; walk with aids; 14y-cognition delay 1 1 Johan den Dunnen
00469181 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00469182 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
00469183 - PubMed: Retterer 2016 analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
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