All individuals with variants in gene BEST1

1875 entries on 19 pages. Showing entries 1 - 100.
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00000102 - PubMed: Almomani 2011 - - - - - - - - - - - 2 1 Global Variome, with Curator vacancy
00000220 PCD206 PubMed: Antony 2013 2-generation family, 1 affected, unaffected parents M - United Kingdom (Great Britain) - - - - - CILD14 - 2 1 Hannah Mitchison
00000221 PCD210 PubMed: Antony 2013 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Afghanistan Pubjabi - - - - CILD14 - 2 1 Hannah Mitchison
00033162 - - - M - - - - - - - retinal disease retinal degeneration, severe, early onset (EOSRD) 1 1 Kornelia Neveling
00033170 - - - F - - - - - - - retinal disease retinal degeneration, severe, early onset (EOSRD) 1 1 Kornelia Neveling
00100088 PKRD141;61141 PubMed: Li 2017 - F yes Pakistan Pakistani - - - - RD - 1 1 James Hejtmancik
00155391 - Sharon, submitted - M yes Israel Arab-Muslim - - - - VMD2 - 1 2 Dror Sharon
00155392 - Sharon, submitted - F no Israel Jewish-Ashkenazi - - - - VMD2 - 1 2 Dror Sharon
00207676 - - - F - - - - - - - retinal disease - 1 1 Marta de Castro-Miró
00207682 - - - M - - - - - - - retinal disease - 1 1 Marta de Castro-Miró
00233202 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00233203 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233204 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233205 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00233206 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 32 Yoshito Koyanagi
00233207 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233208 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 12 Yoshito Koyanagi
00233209 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233773 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00263902 - - - F - - - - - - - ? Macular degeneration (HP:0000608) 1 1 IMGAG
00290459 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00290460 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 13 Mohammed Faruq
00295936 - - - F - - - - - - - ? Macular degeneration (HP:0000608) 1 1 IMGAG
00300619 - - - M - Germany - - - - - ? Abnormality of the eye (HP:0000478) 1 1 Andreas Laner
00300621 - - - F - Germany - - - - - ? Abnormality of the retina (HP:0000479) 1 1 Andreas Laner
00305912 Pat4 PubMed: Marcogliese 2018 2-generation family, 1 affected, unaffected parents F - - - - - - - NDD, VMD no dysmorphisms; motor regression present (age onset unknown); 12y-single words; unsteady gait, clumsy, 12y-mostly wheelchair-bound; 12y-loss of fine motor skills; excessive drooling; 12y-lost continence; 15y-lower extremity dystonia; bilateral ptosis, macular degeneration; 12y-poor balance; Bracken Basics Concepts III Receptive and School Readiness Composite, Conner’s Parent Rating Scale, 6y-Child Behavior Checklist intellectual functioning at approximately 1-3 year level; 13y-epilepsy, spells that consist of falling that last about 1 min; EEG 6.5y-no electrographic or electroclinical sz, but photic stim produced photoconvulsive response, 13y-moderately abnormal - recorded photo myoclonic sz during intermittent photic stim, generalized interictal epileptiform features, sleep architecture was additionally somewhat disrupted with high-voltage rhythmic delta; MRI brain 6y-normal, 13y-normal, 15y-thin corpus callosum but overall within normal limits, MRI brain 13y-spine normal, 15y-spine normal 1 1 Johan den Dunnen
00305959 - - - M - - - - - - - ? Vitelliform-like macular lesions (HP:0007677) 1 1 IMGAG
00308417 CIC05272 PubMed: Boulanger-Scemama 2015 - - - France - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308481 - PubMed: Holtan 2020 2 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00308482 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308483 - PubMed: Holtan 2020 9 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 9 Global Variome, with Curator vacancy
00308484 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308485 - PubMed: Holtan 2020 4 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 4 Global Variome, with Curator vacancy
00308486 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308487 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308601 - PubMed: Holtan 2020 1 homozygous patient - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308602 - PubMed: Holtan 2020 1 homozygous patient - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308633 - PubMed: Holtan 2020 2 homozygous patients - - Norway - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00308674 - PubMed: Kim 2019 - - - Korea - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308735 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00308972 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 2 1 Global Variome, with Curator vacancy
00308973 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308974 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00308975 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308976 - PubMed: Sharon 2019 3 IRD families - - Israel - - - - - retinal disease - 1 3 Global Variome, with Curator vacancy
00308977 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308978 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308979 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308980 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00308981 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308982 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308983 - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - retinal disease - 1 5 Global Variome, with Curator vacancy
00308984 - PubMed: Sharon 2019 4 IRD families - - Israel - - - - - retinal disease - 1 4 Global Variome, with Curator vacancy
00308985 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00325452 3109 PubMed: Zenteno 2020 - - - Mexico - - - - - retinal disease macular dystrophy 1 1 Johan den Dunnen
00328191 G007693 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328253 G009002 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328427 690275 PubMed: Zhou 2018 - - - China - - - - - retinal disease - 1 1 LOVD
00328428 680687 PubMed: Zhou 2018 - - - China - - - - - retinal disease - 1 1 LOVD
00328429 690910 PubMed: Zhou 2018 - - - China - - - - - retinal disease - 1 1 LOVD
00331963 Pat101 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG borderline 1 1 LOVD
00331964 Pat102 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00331965 Pat103 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00331966 Pat104 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG normal 2 1 LOVD
00331967 Pat105 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; scotopic ERG normal; photopic ERG borderline 2 1 LOVD
00332014 Pat152 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; EOG borderline 1 1 LOVD
00332015 Pat153 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced 1 1 LOVD
00332016 Pat154 PubMed: Birtel 2018 family F - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG normal 1 1 LOVD
00332017 Pat155 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease night vision problems; EOG reduced; scotopic ERG normal; photopic ERG normal 1 1 LOVD
00332018 Pat156 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00332019 Pat157 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00332020 Pat158 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced 1 1 LOVD
00332021 Pat159 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG normal 1 1 LOVD
00332022 Pat160 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease metamorphopsia; EOG reduced 1 1 LOVD
00332023 Pat161 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG normal 1 1 LOVD
00332024 Pat162 PubMed: Birtel 2018 family M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normal; photopic ERG borderline 1 1 LOVD
00332025 Pat163 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced 1 1 LOVD
00332026 Pat164 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00332027 Pat165 PubMed: Birtel 2018 patient M - Germany - - - - - retinal disease reduced visual acuity; EOG reduced; scotopic ERG borderline; photopic ERG borderline 1 1 LOVD
00332504 Pat29 PubMed: Avela 2018 - - - Finland - - - - - retinal disease see paper; ... 2 1 LOVD
00333486 patient PubMed: Li 2017 - F - China - - - - - ? see paper; ... 1 1 Johan den Dunnen
00333682 837 PubMed: Stone 2017 family, 2 affected M - (United States) - - - - - retinal disease clinical category IIB 1 2 LOVD
00333683 838 PubMed: Stone 2017 family, 20 affected M - (United States) - - - - - retinal disease clinical category IIB 1 20 LOVD
00333684 839 PubMed: Stone 2017 family, 26 affected F - (United States) - - - - - retinal disease clinical category IIB 1 26 LOVD
00333685 841 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333686 842 PubMed: Stone 2017 family, 2 affected M - (United States) - - - - - retinal disease clinical category IIB 1 2 LOVD
00333687 843 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333688 845 PubMed: Stone 2017 family, 2 affected M - (United States) - - - - - retinal disease clinical category IIB 1 2 LOVD
00333689 846 PubMed: Stone 2017 family, 4 affected M - (United States) - - - - - retinal disease clinical category IIB 1 4 LOVD
00333690 847 PubMed: Stone 2017 1 affected F - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333691 848 PubMed: Stone 2017 1 affected F - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333692 850 PubMed: Stone 2017 family, 5 affected F - (United States) - - - - - retinal disease clinical category IIB 1 5 LOVD
00333693 851 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333694 852 PubMed: Stone 2017 family, 2 affected F - (United States) - - - - - retinal disease clinical category IIB 1 2 LOVD
00333695 853 PubMed: Stone 2017 1 affected F - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333696 857 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333697 858 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333698 859 PubMed: Stone 2017 1 affected F - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00333699 860 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category IIB 1 1 LOVD
00334111 648 PubMed: Stone 2017 1 affected M - (United States) - - - - - retinal disease clinical category II 2 1 LOVD
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