All individuals with variants in gene GATA2

44 entries on 1 page. Showing entries 1 - 44.
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00245811 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245812 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245813 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245814 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245815 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245816 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245817 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245818 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245819 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245820 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245821 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245822 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245823 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245824 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245825 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245826 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245827 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245828 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245829 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245830 - - - - - - - - - - - IMD21 - 1 1 LOVD
00245831 - PubMed: Mansour 2010 3 affected family members M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia 1 1 LOVD
00245832 - PubMed: Mansour 2010 5 affected family members M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia 1 1 LOVD
00245833 - - - - - - - - - - - ADCAD coronary artery disease, association with 1 1 LOVD
00245834 - - - - - - - - - - - Healthy/Control - 4 1 LOVD
00245835 - PubMed: Mansour 2010 - M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia 1 1 LOVD
00245836 - OMIM:var - F - (United Kingdom (Great Britain)) Chinese - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) 1 1 LOVD
00245837 - OMIM:var - F - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) 1 1 LOVD
00245838 - PubMed: Mansour 2010 - M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) 1 1 LOVD
00245839 - OMIM:var - M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia 1 1 LOVD
00245840 - PubMed: Mansour 2010 - M - (United Kingdom (Great Britain)) European - - - - Emberger syndrome Primary lymphoedema associated with a predisposition to acute myeloid leukemia / Sporadic? (parents not tested) 1 1 Pia Ostergaard
00245841 - - - - - - - - - - - ADCAD - 1 1 LOVD
00245842 - - - - - - - - - - - ADCAD - 1 1 LOVD
00245843 - - - - - - - - - - - ADCAD - 1 1 LOVD
00293198 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 36 Mohammed Faruq
00293199 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 9 Mohammed Faruq
00293200 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 13 Mohammed Faruq
00335038 - PubMed: Luo 2021, Journal: Luo 2021 analysis 233 patients - - China - - - - - IMD74 hospitalized after COVID-19 infection, 1 1 Liu Wenbing
00380787 ? PubMed: Nair 2018 - ? - Lebanon - - - - - IMD21 Hearing impairment; motor delay; lower limb edema (Immune/hematology) 1 1 LOVD
00402918 Fam3Pat1 PubMed: Ozen 2017 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Turkey - - - - - CHAPLE see paper; ... 1 1 Johan den Dunnen
00433107 Pat84,1/84,4 PubMed: Stray-Pedersen 2017 2-generation family, affected twin sisters, unaffected heterozygous carrier parents F - Norway - 45y - - - IMD both classic GATA2-related phenotype with disseminated warts and malignant transformation 1 2 Johan den Dunnen
00433109 Pat86,1 PubMed: Stray-Pedersen 2017 - F - Norway - - - - - IMD defect in innate immunity including mucocutaneous candidiasis, hyper IgE syndrome, mendelian susceptibility to mycobacterial disease, and complement deficiency 1 1 Johan den Dunnen
00433111 Pat88,1 PubMed: Stray-Pedersen 2017 - M - Norway - - - - - IMD defect in innate immunity including mucocutaneous candidiasis, hyper IgE syndrome, mendelian susceptibility to mycobacterial disease, and complement deficiency 1 1 Johan den Dunnen
00443658 UCDMX004_S4 - - F - Mexico Mexican - - - - cancer, colon - 1 1 Leticia Angélica Barraza Arellano
00461043 - - - - - Netherlands - - - - - ? - 1 1 Tjakko van Ham
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