All individuals with variants in gene SETD2

20 entries on 1 page. Showing entries 1 - 20.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00016422 - PubMed: Luscan 2014, Journal: Luscan 2014 Molecular Diagnostic Department; adopted child F ? France white >22y - - - MALNS;SOTOS2 postnatal overgrowth, macrocephaly, obesity, speech delay and advanced carpal ossification; craniofacial abnormalities including macrocephaly, long face, slightly down-slanting palpebral fissures, pointed chin 1 1 Eric Pasmant
00016425 - PubMed: Luscan 2014, Journal: Luscan 2014 Molecular Diagnostic Department; unaffected, non-carrier parents M no France white >25y - - - MALNS;SOTOS2 postnatal overgrowth, macrocephaly, obesity, speech delay and advanced carpal ossification; craniofacial abnormalities including long face and macrocephaly 1 1 Eric Pasmant
00101379 27317772-T56-P1 PubMed: Tlemsani 2016, Journal: Tlemsani 2016 2 generation family, 1 affected (1M), unaffected non-carrier parents. M - France - - - - - ? Sotos-like syndrome; Height (+3 SD), OFC (+2.5 SD), Weight (+3 SD); mild-moderate intellectual deficiency (HP:0001256), pragmatic language impairment (HP:0002463), bulbous nose (HP:0000414), hypertelorism (HP:0000316), pointed chin (HP:0000307), normal hands and feet. advanced bone age (HP:0005616), BMI 19.8 (no overweight), 2 café au lait spots (HP:0000957), hyperchromic spots following the lines of >Blaschko (HP:0007402). *T56 sister had overgrowth (HP:0001548), macrocephaly (HP:0000256) and hyperpigmented Blaschko spots (HP:0007402). She had mild learning difficulties but no ID, she is very well socially adapted. She did not carry the mutation. 1 1 Lynn Boekhoudt
00210173 - - - M - Germany - - - - - - HP:0001263 (Global developmental delay) 2 1 Andreas Laner
00261165 Fam2PatI2 (mother) Journal: Fischer-Zirnsak 2019 2-generation family, 4 affected (2F, 2M), unaffected heterozygous carrier parents/relatives F - - - - - - - DD developmental delay/intellectual disability (HP:0012758/HP:0001249); 1 4 Johan den Dunnen
00293415 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 235 Mohammed Faruq
00293416 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304953 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00307258 Patient 64 PubMed: Mendonca 2021 patient with retinoblastoma M - Brazil - - - - - RB1 Bilateral 1 1 Vanessa Mendonça
00307259 Patient 66 PubMed: Mendonca 2021 - F - Brazil - - - - - RB1 Unilateral 1 1 Vanessa Mendonça
00311497 272359 PubMed: Faundes 2018 - - - - - - - - - ? - 1 1 Johan den Dunnen
00311558 260963 PubMed: Faundes 2018 - - - - - - - - - ? - 1 1 Johan den Dunnen
00315023 GDB1546 PubMed: Squeo 2020 analysis 263 cases chromatin-related disorder - - Italy - - - - - ? - 1 1 Johan den Dunnen
00315031 18-2798 PubMed: Squeo 2020 analysis 263 cases chromatin-related disorder - - Italy - - - - - ? - 1 1 Johan den Dunnen
00315044 GDB1433 PubMed: Squeo 2020 analysis 263 cases chromatin-related disorder - - Italy - - - - - ? - 1 1 Johan den Dunnen
00315052 GDB1407 PubMed: Squeo 2020 analysis 263 cases chromatin-related disorder - - Italy - - - - - ? - 1 1 Johan den Dunnen
00435242 260488 - - M ? ? (unknown) - - - - - LLS Autism, Absent speech, Multiple cafe-au-lait spots, Spotty hypopigmentation, Vitiligo, Caries 1 1 Andreas Laner
00436146 266625 - - M no Germany - - - - - LLS Intellectual disability, EEG abnormality, Delayed speech and language development, Neurodevelopmental delay 1 1 Andreas Laner
00438597 HSC0048 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures DEE - 1 1 Johan den Dunnen
00441136 R_4600 - - F ? Poland - - - - - LLS - 1 1 Rafał Płoski
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.