All individuals with variants in gene SEMA4A

70 entries on 1 page. Showing entries 1 - 70.
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00033091 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033093 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033097 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033106 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033110 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033117 - - - M - - - - - - - retinal disease secundary photoreceptor damage due to uveÔtis ODS 1 1 Kornelia Neveling
00033125 - - - F - - - - - - - retinal disease early onset; mild intellectual disability, obesitas 1 1 Kornelia Neveling
00033135 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033138 - - - M - - - - - - - retinal disease hypertension 2 1 Kornelia Neveling
00033143 - - - F - - - - - - - retinal disease diabetes mellitus, hypertension, hearing loss 1 1 Kornelia Neveling
00033144 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033148 - - - M - - - - - - - retinal disease Mantle cell lymphoma 1 1 Kornelia Neveling
00033149 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033153 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033164 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033367 - - - ? ? Pakistan - - - - - Healthy/Control - 1 6 Raheel Qamar
00033368 - - - ? ? Pakistan - - - - - Healthy/Control - 1 11 Raheel Qamar
00033369 - - 2 generation family 1 affected, 2 unaffected carrier parents M no Pakistan - - - - - CORD Fundus granularity, macular degeneration and peripheral retinal pigmentation; Onset Progressive loss of visual acuity and colour vision, night blindness, photophobia and epiphora in bright light 2 1 Raheel Qamar
00033370 - - - ? ? Pakistan - - - - - CORD Fundus granularity, macular degeneration and peripheral retinal pigmentation; Onset Progressive loss of visual acuity and colour vision, night blindness, photophobia and epiphora in bright light 2 1 Raheel Qamar
00033371 - - - ? ? Pakistan - - - - - retinal disease Bony corpuscle-type pigmentation, attenuated blood vessels; Onset Night blindness 2 1 Raheel Qamar
00033372 - - - ? ? Pakistan - - - - - retinal disease Bony corpuscle-type pigmentation, attenuated blood vessels; Onset Night blindness 2 1 Raheel Qamar
00033373 - - - ? ? Pakistan - - - - - Healthy/Control - 1 13 Raheel Qamar
00033374 - - - ? ? Pakistan - - - - - Healthy/Control - 1 9 Raheel Qamar
00033375 - - 2 generation family 4 affected, 2 normal M no Pakistan - - - - - retinal disease Bony corpuscle-type pigmentation, attenuated blood vessels; Onset Night blindness 1 4 Raheel Qamar
00033376 - - - ? ? Pakistan - - - - - retinal disease Bony corpuscle-type pigmentation, attenuated blood vessels; Onset Night blindness 1 1 Raheel Qamar
00033377 - - - ? ? Pakistan - - - - - retinal disease Bony corpuscle-type pigmentation, attenuated blood vessels; Onset Night blindness 1 1 Raheel Qamar
00033378 - - - ? ? Pakistan - - - - - ? blindness 1 1 Raheel Qamar
00231982 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00231983 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00231984 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00231985 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 4 Yoshito Koyanagi
00231986 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00231987 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 147 Yoshito Koyanagi
00231988 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1202 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00231989 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1202 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00231990 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00231991 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233602 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 8 Yoshito Koyanagi
00276092 - - - ? no Spain European Non-Finish ? - - - HNPCC (Lynch) - 1 1 Mariona Terradas
00276094 - - - ? - Spain European Non-Finish - - - - HNPCC (Lynch) - 1 1 Mariona Terradas
00289541 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 23 Mohammed Faruq
00289542 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 170 Mohammed Faruq
00304147 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00308379 CIC05563 PubMed: Boulanger-Scemama 2015, PubMed: Boulanger-Scemama 2019 - - - France - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308380 CIC07563 PubMed: Boulanger-Scemama 2015, PubMed: Boulanger-Scemama 2019 - - - France - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00328419 690899 PubMed: Zhou 2018 - - - China - - - - - retinal disease - 1 1 LOVD
00332050 Pat188 PubMed: Birtel 2018 patient F - Germany - - - - - retinal disease reduced visual acuity; EOG borderline; scotopic ERG normalreduced; photopic ERG borderline 1 1 LOVD
00333355 Pat15 PubMed: Costa 2017 - M - Brazil - - - - - retinal disease see paper; ... 1 1 LOVD
00372645 RP289 PubMed: Xu 2014 patient F - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372694 RP301 PubMed: Xu 2014 - - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372702 QT367 PubMed: Xu 2014 - - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00375421 RP#013 PubMed: Katagiri 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00376785 52 PubMed: Wang 2014 - M - United States - - - - - retinal disease - 1 1 LOVD
00379431 - PubMed: Zhou 2011 - - - China - - - - - retinal disease - 1 1 LOVD
00379700 R0012 PubMed: Wan 2018 - ? - China Han Chinese - - - - retinal disease - 1 1 LOVD
00379706 R0019 PubMed: Wan 2018 - ? - China Han Chinese - - - - retinal disease - 1 1 LOVD
00381642 - PubMed: Eisenberger-2013 - F ? Turkey - - - - - retinal disease - 1 1 LOVD
00381817 - PubMed: Wang-2014 - - - - - - - - - retinal disease - 1 1 LOVD
00386182 RPN-296 PubMed: Rodriguez-Munoz 2020 family fRPN-139, proband M - Spain - - - - - retinal disease - 1 1 LOVD
00386296 RPN-60 PubMed: Rodriguez-Munoz 2020 family fRPN-GB, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00389160 444 PubMed: Weisschuh 2020 Filing key number: 142, unclassified / mixed, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389498 782 PubMed: Weisschuh 2020 Filing key number: 303, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389499 783 PubMed: Weisschuh 2020 Filing key number: 303, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389517 801 PubMed: Weisschuh 2020 Filing key number: 318, autosomal dominant retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389620 904 PubMed: Weisschuh 2020 Filing key number: 381, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00403260 Patient 1 PubMed: Men-2017 - M - (United States) - - - - - retinal disease nystagmus, normal visual attention, and a normal fundus exam. ERG responses were severely decreased 1 1 LOVD
00446997 ARRP-450 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - ? - 1 1 Johan den Dunnen
00447376 STGD-427 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - ? - 1 1 Johan den Dunnen
00447494 ARRP-186 PubMed: Weisschuh 2024 family, 2 affected F - Germany - - - - - ? - 1 2 Johan den Dunnen
00447535 CRD-783 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 2 1 Johan den Dunnen
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