All individuals with variants in gene CENPJ

19 entries on 1 page. Showing entries 1 - 19.
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00000019 - PubMed: Almomani 2011 - - - - - - - - - autism, BMD/DMD, TSC - 1 1 Global Variome, with Curator vacancy
00095095 - - - - no - - - - - - MCPH6 Congenital microcephaly 2 1 Karen Stals
00290864 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00290865 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 29 Mohammed Faruq
00290866 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00290867 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00290868 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295358 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00308741 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00361620 12DG1883 PubMed: Anazi 2017 simplex case M yes Saudi Arabia - - - - - ID not syndromic; global developmental delay, Microcephaly 1 1 Johan den Dunnen
00418892 - - - - - - - - - - - microcephaly - 1 1 Andrea Accogli
00431890 SIDS235 - - F - Switzerland Europe 00y06m - - - SIDS SIDS 1 1 Cordula Haas
00433740 M-238 PubMed: Darvish 2010 family, 2 affected - yes Iran - - - - - microcephaly severe intellectual disability; microcephaly (OFC -4 to -6SD); facial dysmorphism (mall ears, hypertelorism, notched nasal tip, strabismus), developmental delay; joint stiffness (ankles); wheelchair bound; pectus incarnatum; finger deformities; seizure 1 2 Johan den Dunnen
00433779 MCP21 PubMed: Sajid Hussain 2013 family, 1 affected - - Pakistan - - - - - microcephaly microcephaly; unable to speak/read/write 1 1 Johan den Dunnen
00433780 MCP22 PubMed: Sajid Hussain 2013 family, 1 affected - - Pakistan - - - - - microcephaly microcephaly 1 1 Johan den Dunnen
00433781 MCP24 PubMed: Sajid Hussain 2013 family, 1 affected - - Pakistan - - - - - microcephaly microcephaly; friendly behavior, partial self-caring ability, no history of epileptic seizure, no reading/writing skills 1 1 Johan den Dunnen
00433895 FamMC7PatIV1 PubMed: Kraemer 2016 family, 3 affected - yes Pakistan - - - - - microcephaly microcephaly, OFC 43.18cm (SD-7,88); mild intellectual disability 1 3 Johan den Dunnen
00433896 FamMC7PatIV2 PubMed: Kraemer 2016 sib - yes Pakistan - - - - - microcephaly microcephaly, OFC 43.18cm (SD-9,35); severe intellectual disability 1 1 Johan den Dunnen
00433897 FamMC7PatIV3 PubMed: Kraemer 2016 sib - yes Pakistan - - - - - microcephaly microcephaly, OFC 45.7cm (SD-7,48); severe intellectual disability 1 1 Johan den Dunnen
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