All individuals with variants in gene ADAR

26 entries on 1 page. Showing entries 1 - 26.
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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     
00058791 - {PMID23001123:Rice 2012} - - no - Norwegian - - - - AGS - 2 3 Johan den Dunnen
00058792 - {PMID23001123:Rice 2012} - - no - Italian - - - - AGS - 2 1 Johan den Dunnen
00058793 - {PMID23001123:Rice 2012} - - yes - Pakistani - - - - AGS - 2 1 Johan den Dunnen
00058794 - {PMID23001123:Rice 2012} - - no - Brazilian - - - - AGS - 1 1 Carli Tops
00058795 - {PMID23001123:Rice 2012} - - yes - Pakistani - - - - AGS - 1 1 Carli Tops
00058796 - {PMID23001123:Rice 2012} - - no - Indian - - - - AGS - 1 1 Johan den Dunnen
00058797 - {PMID23001123:Rice 2012} - - no - Italian - - - - AGS - 2 1 Johan den Dunnen
00058798 - {PMID23001123:Rice 2012} - - no - White British - - - - AGS - 2 1 Johan den Dunnen
00058799 - {PMID23001123:Rice 2012} Identical Twin 1 - no - Spanish - - - - AGS - 2 1 Johan den Dunnen
00058800 - {PMID23001123:Rice 2012} Identical Twin 2 - no - Spanish - - - - AGS - 2 1 Johan den Dunnen
00058801 - - - - no - European-American - - - - AGS - 1 1 Johan den Dunnen
00210194 - - - F - Germany - - - - - - HP:0011842 (Abnormality of skeletal morphology); HP:0011400 (Abnormal CNS myelination); HP:0000252 (Microcephaly) 1 1 Andreas Laner
00230643 FamPatIII1 PubMed: Zhang 2013 3-generation family, 4 affected (3F, M) M - China - - - - - DSH typical hyperpigmented and hypopigmented macules variable in shape and size on dorsal aspects hands and feet 1 4 Alan Herbert
00230644 Fam1Pat1 PubMed: Liu 2014 5-generation family, 4 affected (2F, 2M) F;M - China - - - - - DSH see paper; ... 1 1 Alan Herbert
00230949 Fam2Pat2 PubMed: Liu 2014 3-generation family, 4 affected (2F, 2M) F;M - China - - - - - DSH see paper; ... 1 4 Johan den Dunnen
00230950 Fam3Pat4 PubMed: Liu 2014 2-generation family, affected father/son M - China - - - - - DSH see paper; ... 1 2 Johan den Dunnen
00230951 Fam4Pat4 PubMed: Liu 2014 3-generation family, 4 affected (2F, 2M) F;M - China - - - - - DSH see paper; ... 1 4 Johan den Dunnen
00230952 Fam5Pat5 PubMed: Liu 2014 3-generation family, 5 affected (3F, 2M) F;M - China - - - - - DSH see paper; ... 1 5 Johan den Dunnen
00230953 Fam6Pat6 PubMed: Liu 2014 4-generation family, 5 affected (3F, 2M) F;M - China - - - - - DSH see paper; ... 1 5 Johan den Dunnen
00230954 Fam7Pat7 PubMed: Liu 2014 3-generation family, 5 affected (3F, 2M) F;M - China - - - - - DSH see paper; ... 1 5 Johan den Dunnen
00274152 Pat18 PubMed: Pronicka 2016 2-generation family, 2 affected brothers F - Poland - - - - - ? involvement basal ganglia; mitochondrial disease criteria score 3; muscle biopsy 2 2 Johan den Dunnen
00289527 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00304146 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00374179 S-2936 PubMed: Ganapathy 2019 - - - India - - - - - ? Developmental delay, microcephaly and Dandy-Walker malformations 1 1 Johan den Dunnen
00374645 S-4896 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00459434 - - - M - - (not applicable) white - - - - NDD HP:0007565, HP:0001250, HP:0001263 1 1 Marketa Wayhelova
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