All individuals with variants in gene PNPT1

22 entries on 1 page. Showing entries 1 - 22.
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     
00155227 29311637-Fam1 PubMed: Saeed 2018 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F yes Pakistan Punjab - - - - obesity severe, early-onset obesity (BMI score ≥3) 1 1 Johan den Dunnen
00282298 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282299 - PubMed: Posey 2016, PubMed: Yang 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00282300 - PubMed: Posey 2016, PubMed: Yang 2013 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00282301 - PubMed: Slavotinek 2015 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282302 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282303 - PubMed: von Ameln 2012 - - - - - - - - - HL - 1 1 Global Variome, with Curator vacancy
00282304 - PubMed: Vedrenne 2012 - - - - - - - - - ? - 1 1 Global Variome, with Curator vacancy
00282305 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282306 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282307 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282308 - PubMed: Slavotinek 2015 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282309 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00282310 - - - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00314707 MCA350 PubMed: Slavotinek 2015 - M - United States - - - - - ? see paper; severe delays, seizures, microcephaly, sensorineural deafness, chorioretinal defect, ... 2 1 Johan den Dunnen
00399866 Pat1 PubMed: Pennisi 2022 - M no - - - - - - ENC see paper; ... 2 1 Johan den Dunnen
00399867 Pat2 PubMed: Pennisi 2022 - M yes - - - - - - ENC see paper; ... 1 1 Johan den Dunnen
00399868 Pat3 PubMed: Pennisi 2022 - F yes - - - - - - ENC see paper; ... 1 1 Johan den Dunnen
00399869 Pat4 PubMed: Pennisi 2022 - F no - - - - - - ENC see paper; ... 2 1 Johan den Dunnen
00399870 Pat5 PubMed: Pennisi 2022 - M no - - - - - - ENC see paper; ... 2 1 Johan den Dunnen
00399871 Pat6 PubMed: Pennisi 2022 - M yes - - - - - - ENC see paper; ... 1 1 Johan den Dunnen
00441469 DXDCHE32 PubMed: Vanniya 2022 2-generation family, 1 affected, unaffected heterozygous parents/relatives F - India - - - - - HL prelingual bilateral profound sensorineural hearing loss, vestibular dysfunction, unilateral progressive vision loss 2 1 Johan den Dunnen
Legend   How to query  


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