All individuals with variants in gene GALNS

23 entries on 1 page. Showing entries 1 - 23.
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00291580 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291581 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00291582 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00291583 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 13 Mohammed Faruq
00308751 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00331457 12DG2624 , 12DG2625 PubMed: Maddirevula 2018 family, 2 affected (F, M) F;M yes - Arab - - - - skeletal dysplasia Global developmental delay, Scoliosis, Short stature, Myopia, Short neck, Malar flatteningYes 1 2 LOVD
00331458 15DG0036 PubMed: Maddirevula 2018 family F yes - Arab - - - - skeletal dysplasia Pectus carinatum, Short stature 1 1 LOVD
00331459 10DG2107, 10DG2108 PubMed: Maddirevula 2018 family, 2 affected (F, M) F;M yes - Arab - - - - skeletal dysplasia Kyphosis, Corneal opacity, Sleep apnea, Inguinal hernia, Short stature, High, narrow palateNo 1 2 LOVD
00385922 V2.15 PubMed: Prasad 2016 - M - - - - - - - ? spondyloepiphyseal dysplasia 2 1 Johan den Dunnen
00385925 V2.49 PubMed: Prasad 2016 - F - - - - - - - MPS mucopolysaccharidosis 1 1 Johan den Dunnen
00386505 - PubMed: Nair 2018 patient - - Lebanon - - - - - ? short stature; severe scoliosis (neurological) 1 1 Johan den Dunnen
00402890 Fam3PatII1 PubMed: Lin 2023, Journal: Lin 2023 2-generation family, 1 affected, unaffected heterozygous parents/relatives M yes Sudan - - - - - MPS, neurodegeneration - 1 1 Barbara Vona
00418704 Fam7 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - MPS4A, NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; cryptorchidism, enuresis; short stature; mild features MPS4A (skeletal phenotype) caused by GALNS variants 2 1 Johan den Dunnen
00419517 9144 PubMed: Marinakis 2021 - M - Greece - - - - - ? - 1 1 Jan Traeger-Synodinos
00455318 GALNS-1 PubMed: Pollard 2013, PubMed: Pollard 2016 - - - United States - - - - - MPS - 1 1 Johan den Dunnen
00455319 GALNS-2 PubMed: Pollard 2013, PubMed: Pollard 2016 - - - United States - - - - - MPS - 2 1 Johan den Dunnen
00456268 Pat46 PubMed: Fernandez-Marmiesse 2014 - M - Spain - - - - - ? see paper; ... 1 1 Johan den Dunnen
00456547 Pat37 PubMed: Fang 2022 - F - China - - - - - MPS attenuated 2 1 Johan den Dunnen
00456548 Pat38 PubMed: Fang 2022 - M - China - - - - - MPS severe 2 1 Johan den Dunnen
00456549 Pat39 PubMed: Fang 2022 - M - China - - - - - MPS severe 2 1 Johan den Dunnen
00456550 Pat40 PubMed: Fang 2022 - F - China - - - - - MPS severe 2 1 Johan den Dunnen
00456551 Pat41 PubMed: Fang 2022 - M - China - - - - - MPS attenuated 2 1 Johan den Dunnen
00456552 Pat42 PubMed: Fang 2022 - F - China - - - - - MPS attenuated 2 1 Johan den Dunnen
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