All individuals with variants in gene TMEM38B

37 entries on 1 page. Showing entries 1 - 37.
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00300374 Fam28 PubMed: Liu 2017 analysis 101 unrelated OI families - - China - - - - - OI - 1 1 Johan den Dunnen
00300375 Fam29 PubMed: Liu 2017 analysis 101 unrelated OI families - - China - - - - - OI - 1 1 Johan den Dunnen
00327455 B40 PubMed: Demir 2021 analysis 43 OI patients M - Turkey - - - - - OI - 1 1 Johan den Dunnen
00331576 11DG0907, 14DG0982 PubMed: Maddirevula 2018 family, 2 affected (2F) F yes - Arab - - - - skeletal dysplasia Recurrent fractures 1 2 LOVD
00331577 09DG00035, 09DG00036 , 10DG2179 , 11DG0676 PubMed: Maddirevula 2018 family, 4 affected (4F) F yes - Arab - - - - skeletal dysplasia Recurrent fractures, Delayed speech and language development 1 4 LOVD
00331578 12DG0244 ,12DG0245 , 12DG0246 , 12DG0830 PubMed: Maddirevula 2018 family, 4 affected (F, 3M) F;M yes - Arab - - - - skeletal dysplasia Recurrent fractures 1 4 LOVD
00331579 14DG2011 PubMed: Maddirevula 2018 family M yes - Arab - - - - skeletal dysplasia Recurrent fractures, Bowing of the legs 1 1 LOVD
00372871 - PubMed: Rubinato 2014 The parents are possibly related.; The 33,892 bp deletion spans exons 1 and 2. It was originally reported as chr9:108444592_108478483del, probably for an earlier genome build. - - Albania - - - - - OI - 1 1 Raymond Dalgleish
00372872 Proband 2 PubMed: Cabral 2016 - - - - Europe - - - - OI - 2 1 Raymond Dalgleish
00372873 P2 PubMed: Cao 2019 - - - China - - - - - OI The authors were contacted for further clarification of the OI type. They stated that the patient could be classified as type 3 according to the 5 types of OI (Bonafe et al., 2015, PMID: 26394607). 2 1 Raymond Dalgleish
00372874 Family 1 PubMed: Lv 2016 - - - China Han - - - - OI - 1 1 Raymond Dalgleish
00372875 OI-F3 IV:2 PubMed: Shaheen 2012 - - - Saudi Arabia - - - - - OI - 1 1 Raymond Dalgleish
00372876 OI-F11 IV:3 PubMed: Shaheen 2012 - - - Saudi Arabia - - - - - OI - 1 1 Raymond Dalgleish
00372877 OI-F13 IV:6 PubMed: Shaheen 2012 - - - Saudi Arabia - - - - - OI - 1 1 Raymond Dalgleish
00372878 P3-IV:1 PubMed: Volodarsky 2013 - - - Israel Bedouin - - - - OI - 1 1 Michael Volodarsky
00372879 P1-II:1 PubMed: Volodarsky 2013 - - - Israel Bedouin - - - - OI - 1 1 Michael Volodarsky
00372880 P2-IV:1 PubMed: Volodarsky 2013 - - - Israel Bedouin - - - - OI - 1 1 Michael Volodarsky
00372881 Proband 1 PubMed: Cabral 2016 - - yes Saudi Arabia - - - - - OI - 1 1 Raymond Dalgleish
00372882 AN_005820 PubMed: Essawi 2018 Additional two sisters of the proband were found homozygous for the same mutation - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372883 AN_005821 PubMed: Essawi 2018 An additional sister and two cousins of the proband were found homozygous for the same mutation - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372884 AN_005822 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372885 AN_005823 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 2 1 Sofie Symoens
00372886 AN_005824 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372887 AN_005825 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372888 AN_005826 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372889 AN_005827 PubMed: Essawi 2018 The probands sister harbors the same homozygous mutation - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372890 AN_005828 PubMed: Essawi 2018 The probands OI diagnosed sister harbors the same homozygous mutation - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372891 AN_005829 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372892 AN_005830 PubMed: Essawi 2018 - - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372893 AN_005831 PubMed: Essawi 2018 Additional 2 cousins were found homozygous for the same deletion - - Palestine - - - - - OI - 1 1 Sofie Symoens
00372894 No. 1 PubMed: Caparros-Martin 2016 - - - Egypt - - - - - OI - 1 1 Raymond Dalgleish
00372896 Proband 3 PubMed: Cabral 2016 - - yes Pakistan - - - - - OI - 1 1 Raymond Dalgleish
00372897 Family 2 PubMed: Lv 2016 The proband also has an affected younger brother. - - China Han - - - - OI - 1 1 Raymond Dalgleish
00372898 No. 44 PubMed: Caparros-Martin 2016 - - - Turkey - - - - - OI - 1 1 Raymond Dalgleish
00466822 Pat109 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI OI4 common variable osteogenesis imperfecta, normal sclerae 1 1 Johan den Dunnen
00466823 Pat110 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI OI4 common variable osteogenesis imperfecta, normal sclerae 1 1 Johan den Dunnen
00466824 Pat111 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI OI3 progressively deforming osteogenesis imperfecta 1 1 Johan den Dunnen
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