All individuals with variants in gene LTBP2

52 entries on 1 page. Showing entries 1 - 52.
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00036088 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036089 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036090 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036091 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036092 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036093 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036094 - - - - - Germany - - - - - ? Sphärophakie 1 1 Andreas Laner
00036095 - - - - - Germany - - - - - ? Sphärophakie 1 1 Andreas Laner
00036096 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036097 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036098 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036099 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036100 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036101 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036102 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00036103 - - - - - Germany - - - - - - - 1 1 Andreas Laner
00081432 - - - - - China Han - - - - OPLL thoracic ossification of the ligamentum flavum; long regional at the thoracic spine 2 1 Xiaochen Qu
00240033 - PubMed: Ali 2009 5-generation family, 3 affecteds - - Pakistan - - - - - GLC3D - 2 3 Ramona Haji-Seyed-Javadi
00240034 - PubMed: Ali 2009 4-generation family, 4 affecteds - - Pakistan - - - - - GLC3D - 2 4 Ramona Haji-Seyed-Javadi
00240035 - PubMed: Ali 2009, PubMed: Firasat 2008 6-generation family, 5 affecteds - - - Gypsy - - - - GLC3D - 2 5 Ramona Haji-Seyed-Javadi
00240036 - PubMed: Désir 2010 unaffected carrier parents - - Macedonia gypsy - - - - MSPKA spherophakia, megalocornea, secondary glaucoma 2 1 Ramona Haji-Seyed-Javadi
00240037 - PubMed: Azmanov 2010 5-generation consanguineous family, 5 affecteds, unaffected carriers - - - Gypsy - - - - GLC3D - 2 5 Ramona Haji-Seyed-Javadi
00240038 - PubMed: Azmanov 2010 unrelated families - - - Gypsy - - - - GLC3D - 1 25 Ramona Haji-Seyed-Javadi
00240039 - PubMed: Khan 2011 2-generation family, 6 affecteds, unaffected carriers - - Saudi Arabia - - - - - MSPKA megalocornea, spherophakia; Ectopia Lentis; glaucoma, secondary 2 6 Ramona Haji-Seyed-Javadi
00240040 - - - - - - Gypsy - - - - GLC3D - 1 1 LOVD
00240041 - PubMed: Ali 2009 6-generation family, 6 affecteds - - Pakistan - - - - - GLC3D - 2 6 Ramona Haji-Seyed-Javadi
00240042 - PubMed: Narooie-Nejad 2009 2-generation family, 2 affecteds - - Iran - - - - - GLC3D - 4 2 Ramona Haji-Seyed-Javadi
00240043 - - - - - - Gypsy - - - - GLC3D - 2 1 LOVD
00240044 - - - - - - Gypsy - - - - GLC3D - 3 1 LOVD
00240045 - - - M - Iran Iranian - - - - MFS ectopia lentis, retinal detachment, mitral valve prolapse, severe pectus excavatum; wrist and thumb sign, plain flat foot, reduced upper segment/lower segment and increased armspan/height 1 1 Ramona Haji-Seyed-Javadi
00240046 - - - - - - - - - - - Healthy/Control - 2 1 LOVD
00240047 - PubMed: Désir 2010 6-generation family, 3 affecteds, unaffected carriers - - Morocco - - - - - MSPKA spherophakia, megalocornea, secondary glaucoma 1 3 Ramona Haji-Seyed-Javadi
00240048 - - - - - - Gypsy - - - - GLC3D - 3 1 LOVD
00240049 - - - - - - Gypsy - - - - GLC3D - 1 1 LOVD
00240050 - - - - - - Gypsy - - - - GLC3D - 2 1 LOVD
00240051 - PubMed: Narooie-Nejad 2009 2-generation family, 1 affected - - Iran - - - - - GLC3D - 2 1 LOVD
00240052 - - - - - Iran - - - - - GLC3D - 1 3 LOVD
00240053 - PubMed: Kumar 2010 4-generation consanguineous family, 3 affecteds, unaffected carriers - - India - - - - - MSPKA microspherophakia, isolated; Ectopia Lentis 4 3 Ramona Haji-Seyed-Javadi
00240054 - PubMed: Kumar 2010 4-generation consanguineous family, 2 affecteds (1 heterozygous for LBTP2:c.3262G>A), unaffected carriers - - India - - - - - MSPKA microspherophakia, isolated; Ectopia Lentis 2 1 LOVD
00240055 - PubMed: Azmanov 2010 isolated patient - - - Gypsy - - - - GLC3D - 2 1 LOVD
00240056 - PubMed: Azmanov 2010 isolated patient - - - Gypsy - - - - GLC3D - 2 1 LOVD
00240057 - - - M - Iran Iranian - - - - WMS3 Ectopia Lentis, microspherophakia, shallow anterior chamber-severe myopia, short stature, brachydactyly, joint stiffness, pulmonary stenosis, aortic stenosis 2 1 Ramona Haji-Seyed-Javadi
00240058 - PubMed: Khan 2011 2-generation family, 2 affecteds, unaffected carriers - - Saudi Arabia - - - - - MSPKA megalocornea, spherophakia; Ectopia Lentis; glaucoma, secondary 2 2 Ramona Haji-Seyed-Javadi
00240059 - PubMed: Khan 2011 2-generation family, 2 affecteds, unaffected carriers - - Saudi Arabia - - - - - MSPKA megalocornea, spherophakia; Ectopia Lentis; glaucoma, secondary 2 2 Ramona Haji-Seyed-Javadi
00240060 - PubMed: Narooie-Nejad 2009 6-generation family, 10 affecteds - - Iran - - - - - GLC3D - 2 10 Ramona Haji-Seyed-Javadi
00291112 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00291113 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 18 Mohammed Faruq
00382117 205 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - GLC3D anterior segment developmental anomalies including glaucoma; MIM, 613086 1 1 LOVD
00385456 13013898 PubMed: Lenassi 2020 retrospective analysis M - (United Kingdom (Great Britain)) - - - - - retinal disease - 2 1 LOVD
00385483 15022428 PubMed: Lenassi 2020 retrospective analysis F - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00385493 16012251 PubMed: Lenassi 2020 retrospective analysis F - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00444098 Fam3PatII2 2-generation family, affected fetus/boy, unaffected heterozygous carrier parents PubMed: Bayam 2024 M yes Saudi Arabia Arab - - - - ? see paper; ..., pregnancy unremarkable; birth term, C-section, weight 3.09kg, length 52cm, OFC 34cm (-0.9 SD); weight 10.5kg (-2.98 SD), length 92cm (-1.32 SD), OFC 44cm (-3.7 SD); global developmental delay; not walking; no clear words; MRI brain 1y-widening bilateral ventricles, basal cisterns and cereberal cortical sulci suggestive of global brain volume loss, periventricular abnormal high signal intensity FLAIR, T1 and T2-weighted images suggestive of periventricular leukomalacia, bbrain appears small in size (microcephaly), corpus callosum very thin; EEG slow background activity, generalized and predominantly anterior spikes of epileptic discharge; no coordination; initial infantile hypotonia progressed to hypertonia/spasticity; hyperreflexia; not able to stand or walk; normal sensory; profound intellectual disability; myoclonic seizures then mixed seizures; persistent head lag, abnormality of ocular smooth pursuit; hypertelorism, medial flaring eye browes, thick upper and lower lips, elevated ear lobules, low auricle; flexion deformity at both ankles/wrists; no anomalies digestive organs; no hert defects; mild hydronephrotic changes in infantile period with normal renal biochemical function; older sibling 6y-deceased, severe neurodevelopmental disease, seizures 1 1 Zafer Yuksel
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