All individuals with variants in gene COL18A1

35 entries on 1 page. Showing entries 1 - 35.
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00074436 - - - F no - white - - Yes - KNO1 - 2 1 Mark Corbett
00103998 Vogelaar-107A PubMed: Vogelaar 2017, Journal: Vogelaar 2017 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer - - - - - - - - cancer, gastric diffuse-type or intestinal-type gastric cancer 1 1 Marjolijn JL Ligtenberg
00293025 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 146 Mohammed Faruq
00293026 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 98 Mohammed Faruq
00293027 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00293028 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 104 Mohammed Faruq
00293029 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 229 Mohammed Faruq
00299641 FamGC3626Pat2 PubMed: Arno 2017 2-generation family, 1 affeted M - - - - - - - retinal disease see paper; ..., 29y-photopsia (HP:0030786), slightly reduced acuity (HP:0007663), mild nyctalopia (HP:0000662); irregular pigmented lesions in periphery(HP:0007703), pale discs (HP:0000543), cystoid macular edema (HP:0011505), peripheral telangiectasia (HP:0007763) with some retinal edema (HP:0020120) and vitreous cells (HP:0004327), possible para-arteriolar sparing; 29y-ERG no identifiable responses other than a minimal, delayed response to 30Hz flicker (PERG, EOG and ERG tested), severe photoreceptor dysfunction; 29y-colour vision Ishihara 15/15 each eye; 29y-Goldmann visual fields ring scotoma at 30 degrees, binocular Esterman age 36: central 20 degrees only retained; presenting VA logMAR (Snellen) R 0.48 (20/60), L 0.3 (20/40); latest VA logMAR R 1.8 (20/1250), L 1.5 (20/630); latest refractive error, dioptres R -1.00/-1.00x5, L +0.75/-1.00x90 1 1 Johan den Dunnen
00304878 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304879 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00304880 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00309106 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00327975 G000988 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328062 G004693 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328236 G008162 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00328304 W000181 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00380143 14DG2133 PubMed: Patel 2018 - - likely Saudi Arabia - - - - - retinal disease - 1 1 LOVD
00383421 - PubMed: Khan 2019 - F - - - - - - - retinal disease - 1 1 LOVD
00383422 - PubMed: Khan 2019 - F - - - - - - - retinal disease - 1 1 LOVD
00387645 33 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - retinal disease - 2 1 LOVD
00390236 G000988 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
00390237 G004693 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
00390238 G008162 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - retinal disease - 2 1 LOVD
00390239 W000181 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - retinal disease - 2 1 LOVD
00447049 CD-1 PubMed: Weisschuh 2024 family, >3 affected M - Germany - - - - - ? - 1 4 Johan den Dunnen
00447206 MISC-296 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00447567 MISC-297 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 2 1 Johan den Dunnen
00447570 MISC-312 PubMed: Weisschuh 2024 family, >3 affected F - Germany - - - - - ? - 2 4 Johan den Dunnen
00447571 MISC-319 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00451560 FamIPatIV3 PubMed: Basharat 2024 4-generation family, 11 affected (4F, 7M) M yes Pakistan - - - - - ? no night vision; perception of light; nystagmus; no corneal haze; no photophobia; mild intellectual disability 1 11 Rabia Basharat
00451561 FamIPatIV4 PubMed: Basharat 2024 relative M yes Pakistan - - - - - ? no night vision; day vision 20/100; normal color vision; nystagmus; no corneal haze; no photophobia; mild intellectual disability 1 1 Rabia Basharat
00451562 FamIPatIV5 PubMed: Basharat 2024 relative M yes Pakistan - - - - - ? no night vision; day vision 20/120; normal color vision; nystagmus; no corneal haze; no photophobia; mild intellectual disability 1 1 Rabia Basharat
00451563 FamIPatIV6 PubMed: Basharat 2024 relative F yes Pakistan - - - - - ? no night vision; day vision 20/120; normal color vision; nystagmus; no corneal haze; no photophobia; mild intellectual disability 1 1 Rabia Basharat
00468446 Pat5 PubMed: Wang 2024 patient, no family history M - China - - - - - CTRCT cortical cataract, pulverulent cataract; symmetrical opacities; macular hypoplasia, high myopia, cardiac defects, joint hypermobility 2 1 Johan den Dunnen
00469580 TabS5-var6 PubMed: Retterer 2016 2-generation family, unaffected heterozygous carrier parents; analysis proband (1/3040); possible combination of variants not reported - - United States - - - - - ? - 1 1 Johan den Dunnen
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