All individuals with variants in gene TOPORS

148 entries on 2 pages. Showing entries 1 - 100.
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00033088 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033091 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033092 - - - M - - - - - - - retinal disease hearing loss 1 1 Kornelia Neveling
00033093 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033107 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033111 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033126 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033129 - - - M - - - - - - - retinal disease onset childhood; retinal degeneration, severe, early onset (EOSRD); Leber congenital amaurosis; tinnitus: BAE normal 1 1 Kornelia Neveling
00033141 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00173886 RP282 PubMed: Xu 2014 - - - United States - - - - - retinal disease - 1 1 Isabelle Audo
00173892 31 PubMed: Wang 2014b - F - United States - - - - - CORD - 1 1 Isabelle Audo
00233117 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1200 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233118 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233119 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233120 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233121 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233122 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00233123 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233124 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233125 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233126 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 4 Yoshito Koyanagi
00233127 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 7 Yoshito Koyanagi
00233128 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233129 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233130 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233765 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00294842 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00294843 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 26 Mohammed Faruq
00294844 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 30 Mohammed Faruq
00308569 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309431 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309432 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00325514 EC17 PubMed: Zenteno 2020 family - - Mexico - - - - - retinal disease retinitis pigmentosa 1 1 Johan den Dunnen
00328092 G005181 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328310 W000191 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00333387 RD14–07 PubMed: Wang 2017 - - - United States - - - - - retinal disease see paper; ... 1 1 LOVD
00334571 349 PubMed: Vincent 2017 patient, no family history F no Samoa - - - - - retinal disease see paper; ... 1 1 LOVD
00335171 9237 PubMed: Haer-Wigman 2017 family - no Netherlands - - - - - ? 58y-diagnosis visual impairment 1 1 LOVD
00335311 Pat50 PubMed: Bravo-Gil 2017 patient - - Spain - - - - - retinal disease see paper; ... 1 1 Nereida Bravo Gil
00335438 RP083 PubMed: Huang 2018 - - - - - - - - - retinal disease see paper; ... 1 1 LOVD
00335450 Fam6 PubMed: Todorova 2017 2-generation family, 2 affected - - Switzerland - - - - - retinal disease congenital nystagmus, rod-cone dystrophy, prominent optic disc with dilated, tortuous, with excessive branching pattern peri- papillary vessels 1 2 Johan den Dunnen
00335590 FAM_048 PubMed: Van Cauwenbergh 2017 - - - Belgium - - - - - retinal disease see paper; ... 1 1 LOVD
00359133 13006275 PubMed: Ellingford 2016 patient - - - - - - - - retinal disease - 1 1 LOVD
00363393 HM785 PubMed: Sun 2015 proband - - China - - - - - retinal disease - 1 1 LOVD
00363396 HM654 PubMed: Sun 2015 proband - - China - - - - - retinal disease - 1 1 LOVD
00363422 - PubMed: Coussa 2015 index patient - - Canada French-Canadian - - - - retinal disease see paper; ... 1 1 LOVD
00363423 - PubMed: Coussa 2015 index patient - - Canada French-Canadian - - - - retinal disease see paper; ... 1 1 LOVD
00363424 - PubMed: Coussa 2015 index patient - - Canada French-Canadian - - - - retinal disease see paper; ... 1 1 LOVD
00372085 XF1 PubMed: Yoon 2015 family - - Korea - - - - - retinal disease see paper; ... 1 1 LOVD
00372497 107 PubMed: Wang 2015 index case - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372640 RP316 PubMed: Xu 2014 patient M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372641 RP021 PubMed: Xu 2014 family M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372668 RP397 PubMed: Xu 2014 patient M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00373488 RP1608 PubMed: Fernandez-San Jose 2015 family, 2 affected - - Spain - - - - - retinal disease see paper; ... 1 2 LOVD
00373869 Rp201 PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - retinal disease see paper; ... 1 1 LOVD
00374930 W136-1 PubMed: Huang 2015 - F - China - - - - - retinal disease best corrected visual acuity 0.8/0.7 1 1 LOVD
00375291 K6210 PubMed: Oishi 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00376747 43 PubMed: Wang 2014 - M - United States - - - - - retinal disease - 1 1 LOVD
00376794 61 PubMed: Wang 2014 - M - United States - - - - - retinal disease - 1 1 LOVD
00376797 64 PubMed: Wang 2014 - F - United States - - - - - retinal disease - 1 1 LOVD
00377168 227 Tracewska 2021, MolVis in press proband F no Poland Slavic - - yes - retinal disease see paper 1 2 LOVD
00377169 441 Tracewska 2021, MolVis in press son M no Poland Slavic - - yes - retinal disease see paper 1 1 LOVD
00377486 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00377487 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00377488 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00379566 - PubMed: O'Sullivan-2012 - - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00381024 - PubMed: Chen-2013 - F - China Chinese - - - - retinal disease - 1 1 LOVD
00381046 - PubMed: Chen-2013 - - - China Chinese - - - - retinal disease - 1 1 LOVD
00381056 - PubMed: Chen-2013 - - - China Chinese - - - - retinal disease - 1 1 LOVD
00381653 - PubMed: Eisenberger-2013 - F no Germany - - - - - retinal disease - 1 1 LOVD
00381655 - PubMed: Eisenberger-2013 - F no Germany - - - - - retinal disease - 1 1 LOVD
00381779 - PubMed: Sullivan-2013 - - no - - - - - - retinal disease - 1 1 LOVD
00381780 - PubMed: Sullivan-2013 - - no - - - - - - retinal disease - 1 1 LOVD
00381789 - PubMed: Sullivan-2013 - - no - - - - - - retinal disease - 1 1 LOVD
00381911 61 PubMed: Birtel 2018 - F - Germany - - - - - retinal disease - 1 1 LOVD
00381912 62 PubMed: Birtel 2018 - F - Germany - - - - - retinal disease - 1 1 LOVD
00382440 269 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 1 1 LOVD
00382605 468 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 1 1 LOVD
00384504 15283 PubMed: Wang 2019 - M - China - - - - - retinal disease - 1 1 LOVD
00386193 RPN-309 PubMed: Rodriguez-Munoz 2020 family fRPN-147, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00389670 954 PubMed: Weisschuh 2020 Filing key number: 424, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389671 955 PubMed: Weisschuh 2020 Filing key number: 424, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389672 956 PubMed: Weisschuh 2020 Filing key number: 424, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389852 1136 PubMed: Weisschuh 2020 Filing key number: 783, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389994 1278 PubMed: Weisschuh 2020 Filing key number: 1095, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00390004 1288 PubMed: Weisschuh 2020 Filing key number: 1135, sporadic retinitis pigmentosa , no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00390404 G005181 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00390405 W000191 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - retinal disease - 1 1 LOVD
00392326 19118 PubMed: Xiao-2021 - F - China - - - - - retinal disease best corrected visual acuity right/left eye: 0.5/0.3, electroretinograhy responses: not available 1 1 LOVD
00392353 19364 PubMed: Xiao-2021 - M - China - - - - - retinal disease best corrected visual acuity right/left eye: 0.8/0.8, electroretinograhy responses: not available 1 1 LOVD
00392389 19937 PubMed: Xiao-2021 - F - China - - - - - retinal disease best corrected visual acuity right/left eye: 0.7/0.7, electroretinograhy responses: extinguished 1 1 LOVD
00392591 47 PubMed: Ma 2021 - ? - Korea - - - - - retinal disease - 1 1 LOVD
00394542 - PubMed: Colombo-2020 - F no - - - - - - retinal disease - 1 1 LOVD
00396422 087384 PubMed: Ellingford 2016 - - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 Johan den Dunnen
00396596 - PubMed: Numa 2020 - M - Japan Japanese - - - - retinal disease night blindness 1 1 LOVD
00416568 1_II:1 PubMed: Chakarova 2007 family 1, individual II:1 F - - Canadian - - - - retinal disease whole cohort description: age at onset: 10-50y, differed between the generations, three affected patients found to be asymptomatic with a completely normal retinal appearance; visual acuities (range 20/20 to finger counting); 16 of 17 had better than 20/40 acuity and 11 of 17 had 20/20 acuity at the most recent visit; visual-field sizes: 10-80 deg; electroretinography abnormalities: highly variable, with early rod dysfunction followed by cone defects; earliest sign of disease (found in four children) - an unusual perivascular cuff of retinal pigment epithelium atrophy, which was found surrounding the superior and inferior arcades; this progressed to a diffuse pigmentary retinopathy with choroidal sclerosis 1 1 LOVD
00416569 1_II:6 PubMed: Chakarova 2007 family 1, individual II:6 F - - Canadian - - - - retinal disease whole cohort description: age at onset: 10-50y, differed between the generations, three affected patients found to be asymptomatic with a completely normal retinal appearance; visual acuities (range 20/20 to finger counting); 16 of 17 had better than 20/40 acuity and 11 of 17 had 20/20 acuity at the most recent visit; visual-field sizes: 10-80 deg; electroretinography abnormalities: highly variable, with early rod dysfunction followed by cone defects; earliest sign of disease (found in four children) - an unusual perivascular cuff of retinal pigment epithelium atrophy, which was found surrounding the superior and inferior arcades; this progressed to a diffuse pigmentary retinopathy with choroidal sclerosis 1 1 LOVD
00416570 1_III:1 PubMed: Chakarova 2007 family 1, individual III:1 F - - Canadian - - - - retinal disease whole cohort description: age at onset: 10-50y, differed between the generations, three affected patients found to be asymptomatic with a completely normal retinal appearance; visual acuities (range 20/20 to finger counting); 16 of 17 had better than 20/40 acuity and 11 of 17 had 20/20 acuity at the most recent visit; visual-field sizes: 10-80 deg; electroretinography abnormalities: highly variable, with early rod dysfunction followed by cone defects; earliest sign of disease (found in four children) - an unusual perivascular cuff of retinal pigment epithelium atrophy, which was found surrounding the superior and inferior arcades; this progressed to a diffuse pigmentary retinopathy with choroidal sclerosis 1 1 LOVD
00416571 1_III:2 PubMed: Chakarova 2007 family 1, individual III:2 M - - Canadian - - - - retinal disease whole cohort description: age at onset: 10-50y, differed between the generations, three affected patients found to be asymptomatic with a completely normal retinal appearance; visual acuities (range 20/20 to finger counting); 16 of 17 had better than 20/40 acuity and 11 of 17 had 20/20 acuity at the most recent visit; visual-field sizes: 10-80 deg; electroretinography abnormalities: highly variable, with early rod dysfunction followed by cone defects; earliest sign of disease (found in four children) - an unusual perivascular cuff of retinal pigment epithelium atrophy, which was found surrounding the superior and inferior arcades; this progressed to a diffuse pigmentary retinopathy with choroidal sclerosis 1 1 LOVD
00416572 1_III:4 PubMed: Chakarova 2007 family 1, individual III:4 M - - Canadian - - - - retinal disease whole cohort description: age at onset: 10-50y, differed between the generations, three affected patients found to be asymptomatic with a completely normal retinal appearance; visual acuities (range 20/20 to finger counting); 16 of 17 had better than 20/40 acuity and 11 of 17 had 20/20 acuity at the most recent visit; visual-field sizes: 10-80 deg; electroretinography abnormalities: highly variable, with early rod dysfunction followed by cone defects; earliest sign of disease (found in four children) - an unusual perivascular cuff of retinal pigment epithelium atrophy, which was found surrounding the superior and inferior arcades; this progressed to a diffuse pigmentary retinopathy with choroidal sclerosis 1 1 LOVD
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