All individuals with variants in gene BMP1

29 entries on 1 page. Showing entries 1 - 29.
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00050314 - PubMed: DDDS 2015, Journal: DDDS 2015 uninherited diplotypes - - United Kingdom (Great Britain) - - - - - ? severe undiagnosed developmental disorders 1 1 Johan den Dunnen
00100647 @DRN - - M no (Italy) white - - yes surgery of cranial posterior fossa CM1 hypertelorism, prominent head, epicanthus, clinodactyly, psycho-motor delay 1 2 Patrizia De Marco
00294619 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 199 Mohammed Faruq
00305194 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00372585 - PubMed: Asharani 2012 The patient, whose parents are first cousins, is described as having an OI-like disease. An analysis of bone tissue from this patient (or from his sibling?) was presented subsequently by {PMID24091809:Hoyer-Kuhn et al., 2014}. - - Turkey - - - - - OI - 1 1 Raymond Dalgleish
00372586 - PubMed: Valencia 2014 - - - Pakistan - - - - - OI3, OI4 - 1 1 Victor L Ruiz-Perez
00372587 - PubMed: Syx 2015 - - - Portugal - - - - - OI, OI4 - 2 1 Raymond Dalgleish
00372588 - PubMed: Syx 2015 Patient P3 has a brother (P4) harbouring the same sequence variants. - - Scotland - - - - - OI - 2 1 Raymond Dalgleish
00372589 - {PMID29499418 : Mrosk 2018} - - - India - - - - - OI - 1 1 Raymond Dalgleish
00372590 - PubMed: Xu 2019 - - - China Han - - - - OI7 - 2 1 Raymond Dalgleish
00372591 - PubMed: Essawi 2018, Journal: Essawi 2018 - - yes Palestine - - - - - OI3, OI4 - 1 1 Sofie Symoens
00372593 - PubMed: Essawi 2018, Journal: Essawi 2018 - - yes Palestine - - - - - OI, OI1 - 1 1 Sofie Symoens
00372595 - PubMed: Martínez-Glez 2012 - - - Egypt - - - - - OI3 - 1 1 Victor L Ruiz-Perez
00372596 - PubMed: Sangsin 2017 - - - Thailand - - - - - OI - 2 1 Raymond Dalgleish
00372597 - PubMed: Cho 2014 - - - Korea - - - - - OI, OI3 - 2 1 Sung Yoon Cho
00372598 - PubMed: Essawi 2018, Journal: Essawi 2018 - - yes Palestine - - - - - OI, OI2, OI3 - 1 1 Sofie Symoens
00372599 - PubMed: Syx 2015 - - - - white - - - - OI3 - 2 1 Raymond Dalgleish
00372600 - PubMed: Pollitt 2016 - - - - - - - - - OI - 2 1 Raymond Dalgleish
00372601 P1 PubMed: Fahiminiya 2014 patient has a younger brother who harbours the same PLS3 variant - - - - - - - - osteoporosis - 1 1 Raymond Dalgleish
00372602 - PubMed: Fahiminiya 2014 - - - Canada French-Canadian - - - - ? Bone fragility 2 1 Raymond Dalgleish
00372603 P1 PubMed: Pollitt 2016 family, 2 affected brothers, both have a severe progressive form of OI - - - - - - - - OI - 1 2 Raymond Dalgleish
00372604 P2 PubMed: Pollitt 2016 brother of P1, harboring the same variation; both individuals have a severe progressive form of OI - - - - - - - - OI - 1 1 Raymond Dalgleish
00372605 - PubMed: Mohd Nawawi 2018 WNT1 sequence variants are normally recessive. The single variant in this patient probably does not account alone for the OI phenotype. - - Malaysia - - - - - OI3 - 1 1 Raymond Dalgleish
00372606 - PubMed: Mrosk 2018 - - - India - - - - - OI - 1 1 Raymond Dalgleish
00372607 - PubMed: Fahiminiya 2014 - - - Canada French-Canadian - - - - ? Bone fragility 1 1 Raymond Dalgleish
00372608 - PubMed: Fahiminiya 2014 - - - Canada French-Canadian - - - - ? Bone fragility 1 1 Raymond Dalgleish
00372609 - PubMed: Fahiminiya 2014 - - - Canada French-Canadian - - - - ? Bone fragility 1 1 Raymond Dalgleish
00410168 Pat1 PubMed: Kuptanon 2022, Journal: Kuptanon 2022 - M no Thailand - - - - - OI13 Dentinogenesis imperfecta (HP:0000703), no Blue sclerae (-HP:0000592), no Hearing abnormality (-HP:0000364) 2 1 Thanakorn Theerapanon
00466828 Pat115 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI OI1 classic non-deforming osteogenesis imperfecta, blue sclerae 1 1 Johan den Dunnen
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