All individuals with variants in gene TRIP11

15 entries on 1 page. Showing entries 1 - 15.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00132077 1 - - M no Brazil - - - - - ACG1A - 2 1 Karina Silveira
00291144 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 12 Mohammed Faruq
00291145 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 37 Mohammed Faruq
00291146 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00291147 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 15 Mohammed Faruq
00291148 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 144 Mohammed Faruq
00304452 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304453 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00326447 - - - F no Argentina - - - - - ODCD - 2 1 Karen E. Heath
00326506 - family, 2 affected siblings - - - - - - - - - ODCD - 2 2 Karen E. Heath
00326507 - - - - - - - - - - - ODCD - 2 1 Karen E. Heath
00331585 15DG1394 PubMed: Maddirevula 2018 family M yes - Arab - - - - skeletal dysplasia Skeletal dysplasia, Abdominal distention, Limb undergrowth 1 1 LOVD
00331586 16DG0956 PubMed: Maddirevula 2018 family M yes - Arab - - - - skeletal dysplasia Skeletal Dysplasia, Stillbirth 1 1 LOVD
00331587 11DG0205 PubMed: Maddirevula 2018 family F yes - Arab - - - - skeletal dysplasia Thoracic hypoplasia, Recurrent fractures, Blue sclerae, Hepatomegaly, Skeletal dysplasia 1 1 LOVD
00469800 Fam127 PubMed: Jacob 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents - - India - - - - - skeletal dysplasia - 3 1 Johan den Dunnen
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