All individuals with variants in gene POMGNT2

23 entries on 1 page. Showing entries 1 - 23.
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00056445 - - 4-generation family, 1 affected M yes Jordan - <1m - - - WWS cobbelstone lissencephaly, enlarged ventricles, cerebellar hypolplasia, retinal dysplasia, hypotonia 2 1 Johan den Dunnen
00056446 - - 4-generation family, unaffected carier parents M;F yes Jordan - - - - - Healthy/Control - 1 2 Johan den Dunnen
00056447 - - 4-generation family, 1 affected F yes Saudi Arabia - <1m - - - WWS cobbelstone lissencephaly, enlarged ventricles, cerebellar hypolplasia, microphthalmia, macrophthalmia, hypotonia 2 1 Johan den Dunnen
00056448 - - 4-generation family, unaffected carier parents M;F yes Saudi Arabia - - - - - Healthy/Control cobbelstone lissencephaly, enlarged ventricles, cerebellar hypolplasia, microphthalmia, macrophthalmia, hypotonia 1 2 Johan den Dunnen
00056449 - - 2-generation family, fetus 1 F ? India - <0d - - - WWS cobbelstone lissencephaly, enlarged ventricles, cerebellar hypolplasia; 23w-terminated pregnancy ventricular enlargement 2 1 Johan den Dunnen
00056450 - - 2-generation family, fetus 2 F ? India - <0d - - - WWS cobbelstone lissencephaly, enlarged ventricles, cerebellar hypolplasia; 20w-terminated pregnancy ventricular enlargement 2 1 Johan den Dunnen
00056451 - - 2-generation family, unaffected carrier parents M;F ? India - - - - - Healthy/Control - 1 2 Johan den Dunnen
00080890 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MDDGA8 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8 (OMIM:614830) 1 1 Daniel Trujillano
00104053 - - - - - - - - - - - MDDGA9 - 2 1 Céline Bouchet Seraphin
00134082 96042 - family, 2 affected siblings M yes Syria - 08y - - - MMDD global developmental delay, muscular hypotonia, joint contractures (leg), no speech, hydrocephalus, cryptochism, CK elevation (2500 U/l) 1 2 Andreas Laner
00274315 Fam1255 PubMed: Reddy 2017 - M - United States - - - - - LGMD - 2 1 Johan den Dunnen
00293387 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293388 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00293389 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00361569 10DG2024 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID syndromic; global developmental delay, occipital encephalocele and hydronephrosis 1 1 Johan den Dunnen
00374813 S-3015 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00374814 S-2393 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00392518 Case 37 - - F no (Korea, South (Republic)) Korea - - - - MDDGA - 1 1 Young Jun Ko
00392549 Case 38 - - M no (Korea, South (Republic)) Korea - - - - MDDGA - 1 1 Young Jun Ko
00408684 Pat27 PubMed: Thomas 2022 no family history - yes France - - - - - NMD - 1 1 Johan den Dunnen
00430410 D21 PubMed: Cavdarli 2023 analysis 146 neuromuscular disease patients F - Turkey - - - - - NMD hypotonia; MRI cranial Dandy walker malformation 1 1 Johan den Dunnen
00438488 D21 PubMed: Cavdarli 2023 analysis 67 patients muscular dystrophy/myopathy (not DMD) F - Turkey - - - - - MD hypotonia, cranial mri: dandy walker malformation 1 1 Johan den Dunnen
00460249 Pat20 PubMed: Marti 2025 patient, no family history - - Spain - - - - - hCK asymptomatic, hyperCKemia; elevated CK level 480-1500 UI/L 1 1 Johan den Dunnen
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