All individuals with variants in gene ABAT

10 entries on 1 page. Showing entries 1 - 10.
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AscendingIndividual ID     

ID_report     

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Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

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Phenotype details     

Variants     

Panel size     

Owner     
00291567 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291573 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 170 Mohammed Faruq
00291574 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 233 Mohammed Faruq
00291575 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 20 Mohammed Faruq
00304545 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00304546 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00361504 13DG1093 PubMed: Anazi 2017 simplex case M yes Saudi Arabia - - - - - ID syndromic; global developmental delay with hypotonia , seizures and dysmorphism 1 1 Johan den Dunnen
00387805 M8700022 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes - Zaboli - - - - ID syndromic intellectual disability, microcephaly 1 2 Johan den Dunnen
00448185 Pat48 PubMed: Poli 2024 - M - Chile - - - - - ? polyhydramnios; decreased fetal movement; seizures. deceased. two affected siblings, deceased. 1 1 Johan den Dunnen
00453028 Fam5 Journal: Paracha 2024 4-generation family, 2 affected sisters,, heterozygous carrier parents/relatives F yes Pakistan - - - - - NDD moderate intellectual disability, development delay, speech problems, aggressive behavior 1 2 Muhammad Umair
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