All individuals with variants in gene G3BP2

9 entries on 1 page. Showing entries 1 - 9.
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00327463 M69 II-1 Doucette 2021, Submitted Affected sister in a 4 member family. Brother is reportedly affected however we were unable to examine him. Parents are both unaffected, presuming recessive inheritance pattern. F - Canada Middle eastern origin - - Yes - retinal degeneration Fundus findings: Circumscribed central retinal atrophy (Retinal atrophy HP:0001105) Ocular coherence tomography (OCT): Atrophy of outer retina. Bruch's membrane is absent in the central fovea. Electroretinogram: Normal ffERG in the right eye; reduced cone flash and flicker in the left eye (Abnormal ERG HP:0000512) 1 2 Lance P Doucette
00470348 118517 PubMed: Jia 2022, PubMed: Joanna 2020 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., intellectual disability, deveopmental delay 1 1 Johan den Dunnen
00470349 DDD4K.01415 PubMed: Jia 2022, PubMed: McRae 2017 2-generation family, 1 affected, unaffected non-carrier parents - - United Kingdom (Great Britain) - - - - - NDD see paper; ..., intellectual disability, deveopmental delay 1 1 Johan den Dunnen
00470350 49254 PubMed: Jia 2022, PubMed: Joanna 2020 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., intellectual disability, deveopmental delay 1 1 Johan den Dunnen
00470351 12523.p1 PubMed: Jia 2022, PubMed: Iossifov 2014 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., autism spectrum disorder 1 1 Johan den Dunnen
00470352 113530 PubMed: Jia 2022, PubMed: Joanna 2020 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., intellectual disability, deveopmental delay 1 1 Johan den Dunnen
00470353 DDD4K.03714 PubMed: Jia 2022, PubMed: McRae 2017 2-generation family, 1 affected, unaffected non-carrier parents - - United Kingdom (Great Britain) - - - - - NDD see paper; ..., intellectual disability, deveopmental delay 1 1 Johan den Dunnen
00470354 2-1261-003 PubMed: Jia 2022, PubMed: Yuen 2017 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., autism spectrum disorder 1 1 Johan den Dunnen
00470355 MAC961 PubMed: Jia 2022, PubMed: Satterstrom 2020 2-generation family, 1 affected, unaffected non-carrier parents - - - - - - - - NDD see paper; ..., autism spectrum disorder 1 1 Johan den Dunnen
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