All individuals with variants in gene PRICKLE1

29 entries on 1 page. Showing entries 1 - 29.
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     
00116834 S_158:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00116839 S_170:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00116843 S_176:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00116884 S_272:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00116886 S_274:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00117003 S_532:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00117012 S_561:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00117058 S_631:0/1:TYPICAL_RE PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 194 RE cases - - - - - - - - epilepsy, Rolandic typical Rolandic epilepsy 1 1 Dheeraj Bobbili
00117066 S_652:0/1:TYPICAL_RE PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 194 RE cases - - - - - - - - epilepsy, Rolandic typical Rolandic epilepsy 1 1 Dheeraj Bobbili
00117103 S_737:0/1:TYPICAL_RE PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 194 RE cases - - - - - - - - epilepsy, Rolandic typical Rolandic epilepsy 1 1 Dheeraj Bobbili
00117120 S_86:0/1:CONTROL PubMed: Bobbili 2018, Journal: Bobbili 2018 individual from 567 controls - - - - - - - - Healthy/Control - 1 1 Dheeraj Bobbili
00222900 - - - M - United States white - - - - ? caudal agenesis: a heterogeneous constellation of anomalies comprising total or partial agenesis of the spinal column, anal imperforation, genital anomalies, bilateral renal dysplasia or aplasia, pulmonary hypoplasia, and lower limb abnormalities 1 1 Zoha Kibar
00222901 - - - F - Italy - - - - - ? diastematomyelia type II: complex dysraphic state caused by failure midline integration notochord leading to variably elongated separation spinal cord in two hemicords (Rossi et al., 2004) 1 1 Zoha Kibar
00222902 - - - M - United States - - - - - ? Lumbosacral myelomeningocele 1 1 Zoha Kibar
00222903 - - - - - United States - - - - - ? Lumbosacral myelomeningocele 1 1 Zoha Kibar
00222904 - - - M - Italy Italian - - - - ? Lumbosacral myelomeningocele, Chiari II malformation 1 1 Zoha Kibar
00222905 - - - M - Italy Italian - - - - ? lumbosacral myelomeningocele, hydrocephalus, Chiari type II malformation 1 1 Zoha Kibar
00222906 - - - - - United States - - - - - ? myelomeningocele 1 1 Zoha Kibar
00222907 - - - M - United States white - - - - ? myelomeningocele 1 1 Zoha Kibar
00222908 - - - M - United States white - - - - ? myelomeningocele 1 1 Zoha Kibar
00222909 - - - M - United States white - - - - ? myelomeningocele 1 1 Zoha Kibar
00222910 FamA PubMed: Bassuk 2008 6-generation family, 8 affecteds - yes Israel Middle-East - - - - EPM1B - 1 8 LOVD
00222911 FamB PubMed: Bassuk 2008 6-generation family, 15 affecteds - yes Israel;Jordan Middle-East - - - - EPM1B - 1 15 LOVD
00222912 FamC PubMed: Bassuk 2008 6-generation family, 3 affecteds - yes Israel Middle-East - - - - EPM1B - 1 3 LOVD
00222913 Pat2 PubMed: Tao 2011 - M - United States - - - - - EPM1B myoclonic seizures, generalized EEG pattern, mild mental retardation 1 1 LOVD
00222914 Pat3 PubMed: Tao 2011 - F - United States - - - - - EPM1B juvenile myoclonic epilepsy 1 1 LOVD
00290697 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295997 - - - F - - - - - - - ? Intellectual disability (HP:0001249); Seizures (HP:0001250); Ataxia (HP:0001251) 1 1 Andreas Laner
00374886 S-3739 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 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.