All individuals with variants in gene YARS2

14 entries on 1 page. Showing entries 1 - 14.
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AscendingIndividual ID     

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00037443 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037444 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037445 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00037446 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00204192 - - - - - Lebanon Lebanese - - - - MLASA2 - 1 1 Isabelle Thiffault
00204193 - PubMed: Riley 2010 - M yes Lebanon Lebanese - - - - MLASA2 - 2 1 LOVD
00204194 - PubMed: Riley 2010 Sister of II:2 F yes Lebanon Lebanese - - - - MLASA2 - 2 1 LOVD
00204195 - PubMed: Riley 2010 parents of II:2 and II:3, the parents are first cousins ? yes Lebanon Lebanese - - - - - - 1 2 LOVD
00204196 - PubMed: Riley 2010 A maternal aunt is said to have had transfusion-dependent sideroblastic anemia and a skeletal myopathy, but never had a muscle biopsy. Brothers & sisters are healthy F yes Lebanon Lebanese - - - - MLASA2 - 2 1 LOVD
00295479 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00296589 Pat22 PubMed: Kemp 2011, PubMed: Taylor 2014 - M yes Lebanon - 37y - - - ? deceased; muscle not affected; central nervous system not affected; heart not affected; liver not affected; Exercise intolerance, sideroblastic anaemia, lactic acidosis 1 1 Johan den Dunnen
00309878 Patient 1 PubMed: Zehravi 2021 - M yes Pakistan Asian - - Yes No RMD2;LGMD1C Proximal muscle weakness of lower limbs (HP:0008994), Toe walking (HP:0040083), Frequent falls (HP:0002527), Myalgia (HP:0003326), Gowers sign (HP:0003391), Hyperlordosis (HP:0003307), Calf muscle pseudohypertrophy (HP:0003707), Flexion contracture (HP:0001371), Elevated serum creatinine kinase (HP:0003236), EMG abnormality (HP:0003457) 1 1 Mehwish Zehravi
00310208 Patient 3 PubMed: Zehravi 2021 - M yes Pakistan Asian - - Yes None RMD2;LGMD1C Muscle weakness (HP:0001324), Progressive muscle weakness (HP:0003323),Difficulty climbing stairs (HP:0003551), Difficulty walking (HP:0002355), Toe walking (HP:0040083), Frequent falls (HP:0002527), Myalgia (HP:0003326), Gowers sign (HP:0003391), Hyperlordosis (HP:0003307), Calf muscle pseudohypertrophy (HP:0003707), Flexion contracture (HP:0001371), Elevated serum creatinine kinase (HP:0003236), EMG abnormality (HP:0003457) 1 1 Mehwish Zehravi
00454651 patient PubMed: Ardissone 2016 2-generation family, affected brother/sister, unaffected heterozygous carrier parents F;M no Italy - - - - - MYOP see paper; ..., anemia, lactic acidemia, required periodic blood transfusions; normal cognitive/motor development 1 2 Johan den Dunnen
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