All individuals with variants in gene NRL

150 entries on 2 pages. Showing entries 1 - 100.
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00033161 - - - M - - - - - - - retinal disease lumped pigmentary retinal degeneration, early onset; ferriprive anemia 2 1 Kornelia Neveling
00105017 69ORG1 PubMed: de Castro-Miró 2016 - M yes Saudi Arabia - - - - - ESCS - 1 1 Marta de Castro-Miró
00155514 - Sharon, submitted - F yes Israel Jewish-Oriental - - - - retinal disease - 1 2 Dror Sharon
00155515 - Sharon, submitted - F no Israel Jewish-Oriental - - - - retinal disease - 1 1 Dror Sharon
00233238 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233239 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233240 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233241 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233242 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00233775 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00291016 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00308525 - PubMed: Holtan 2020 3 patients with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 3 Global Variome, with Curator vacancy
00309258 MOL1109 PubMed: Beryozkin 2015, PubMed: Sharon 2019 family - - Israel Iraq;Jewish - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309259 - PubMed: Sharon 2019 3 IRD families - - Israel - - - - - retinal disease - 1 3 Global Variome, with Curator vacancy
00309260 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00319836 - PubMed: Milla 2002 - - - Spain - - - - - retinal disease - 1 2 Julia Lopez
00325419 1031 PubMed: Zenteno 2020 family - - Mexico - - - - - retinal disease retinitis pigmentosa 1 1 Johan den Dunnen
00326682 - PubMed: Ziviello 2005 - - - Italy - - - - - retinal disease - 1 1 Julia Lopez
00326686 - PubMed: Ziviello 2005 - - - Italy - - - - - retinal disease - 1 1 Julia Lopez
00328492 15004850 PubMed: Taylor 2017 no family history retinal disease M - United Kingdom (Great Britain) - - - - - retinal disease retinal dystrophy (HP:0000556) 1 1 LOVD
00332286 Fam31PatFBP_169 PubMed: Porto 2017 proband - - Brazil - - - - - retinal disease - 2 1 LOVD
00335130 1893 PubMed: Haer-Wigman 2017 patient - yes Netherlands - - - - - ? - 2 1 LOVD
00335644 - PubMed: Sullivan 2006 2 families - - United States - - - - - retinal disease - 1 1 Julia Lopez
00335645 - PubMed: Sullivan 2006 1 family - - United States - - - - - retinal disease - 1 1 Julia Lopez
00335981 - PubMed: Sergouniotis 2016 analysis 486 cases - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00358730 - PubMed: Carrigan 2016 - - - Ireland - - - - - retinal disease see paper; ... 2 1 LOVD
00358731 - PubMed: Carrigan 2016 - - - Ireland - - - - - retinal disease see paper; ... 2 1 LOVD
00359139 13010253 PubMed: Ellingford 2016 patient - - - - - - - - retinal disease - 1 1 LOVD
00373875 OGI-019-047 PubMed: Consugar 2015 - - - United States - - - - - retinal disease see paper; ... 2 1 LOVD
00375300 K2291 PubMed: Oishi 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00376823 UTAD198 PubMed: Daiger 2014 - - - United States - - - - - retinal disease - 1 1 LOVD
00377208 303 Tracewska 2021, MolVis in press proband M no Poland Slavic - - yes - retinal disease see paper 1 3 LOVD
00377209 304 Tracewska 2021, MolVis in press father M no Poland Slavic - - yes - retinal disease see paper 1 1 LOVD
00377210 825 Tracewska 2021, MolVis in press paternal grandmother F no Poland Slavic - - yes - retinal disease see paper 1 1 LOVD
00377268 406 Tracewska 2021, MolVis in press proband F no Poland Slavic - - yes - retinal disease see paper 1 1 LOVD
00377389 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00377390 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00377391 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00379385 - PubMed: Collin-2011 - M - Netherlands - - - - - retinal disease - 1 1 LOVD
00383450 - PubMed: Khan 2019 - M - - - - - - - retinal disease - 1 1 LOVD
00383451 - PubMed: Khan 2019 - F - - - - - - - retinal disease - 1 1 LOVD
00384636 Family 14 patient 1 PubMed: Ehrenberg 2019 - ? no Israel - - - - - ? enhanced S-cone syndrome (AR) and Early onset oculopharyngeal muscular dystrophy (AD) 1 1 LOVD
00384637 Family 15 patient 1 PubMed: Ehrenberg 2019 - ? no Israel - - - - - ? enhanced S-cone syndrome (AR) and Early onset oculopharyngeal muscular dystrophy (AD) 1 1 LOVD
00385040 19653 PubMed: Xu 2020 - ? no China - - - - - retinal disease nyctalopia, no nystagmus, best corrected visual acuity right/left eye: NA 1 1 LOVD
00386979 5 PubMed: Jauregui 2020 - M - (United States) white - - - - retinal disease - 1 1 LOVD
00389860 1144 PubMed: Weisschuh 2020 Filing key number: 797, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00389954 1238 PubMed: Weisschuh 2020 Filing key number: 998, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 2 1 LOVD
00390771 - PubMed: Booij-2011 - - - - - - - - - retinal disease - 1 1 LOVD
00391581 80 PubMed: Hull 2020 - ? - New Zealand Maori - - - - retinal disease - 1 1 LOVD
00392636 117 PubMed: Ma 2021 - ? - Korea - - - - - retinal disease - 1 1 LOVD
00407357 RP-645 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 1 1 LOVD
00407359 RP-65 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 1 1 LOVD
00409947 famRP251pat_III:1 PubMed: Bessant 1999 Family RP251 F - - - - - - - retinal disease - 1 1 LOVD
00409948 famRP251pat_III:3 PubMed: Bessant 1999 Family RP251 F - - - - - - - retinal disease - 1 1 LOVD
00409949 famRP251pat_III:5 PubMed: Bessant 1999 Family RP251 F - - - - - - - retinal disease - 1 1 LOVD
00409950 famRP251pat_III:6 PubMed: Bessant 1999 Family RP251 F - - - - - - - retinal disease - 1 1 LOVD
00409951 famRP251pat_III:7 PubMed: Bessant 1999 Family RP251 M - - - - - - - retinal disease - 1 1 LOVD
00409952 famRP251pat_III:9 PubMed: Bessant 1999 Family RP251 M - - - - - - - retinal disease - 1 1 LOVD
00409953 famRP251pat_III:11 PubMed: Bessant 1999 Family RP251 M - - - - - - - retinal disease - 1 1 LOVD
00409954 famRP357pat_III:3 PubMed: Bessant 2000 Family RP357 M - United Kingdom (Great Britain) south-east England - - - - retinal disease - 1 1 LOVD
00409955 famRP357pat_IV:4 PubMed: Bessant 2000 Family RP357 M - United Kingdom (Great Britain) south-east England - - - - retinal disease - 1 1 LOVD
00409956 famRP57pat_IV:3 PubMed: Bessant 2000 Family RP57 F - United Kingdom (Great Britain) south-east England - - - - retinal disease - 1 1 LOVD
00409957 famRP57pat_V:1 PubMed: Bessant 2000 Family RP57 M - United Kingdom (Great Britain) south-east England - - - - retinal disease - 1 1 LOVD
00409958 famRP3097pat_II:4 PubMed: Bessant 2000 Family RP3097 M - United Kingdom (Great Britain) south-east England - - - - retinal disease - 1 1 LOVD
00409959 fam1pat_III:2 PubMed: Martinez-Gimeno 2001 - F - Spain 10 - - - - retinal disease cataracts at the beginning of the fourth decade; peripheral visual field constriction and pigmentary deposits first occurred at the beginning of the third decade; electroretinography: abolished rod and cone responses 1 1 LOVD
00409960 fam1pat_III:3 PubMed: Martinez-Gimeno 2001 - M - Spain 10 - - - - retinal disease cataracts at the beginning of the fourth decade; peripheral visual field constriction and pigmentary deposits first occurred at the beginning of the third decade; electroretinography: abolished rod and cone responses 1 1 LOVD
00409961 fam1pat_IV:5 PubMed: Martinez-Gimeno 2001 - F - Spain 11 - - - - retinal disease electroretinography: abolished rod and cone responses 1 1 LOVD
00409962 fam1pat_IV:7 PubMed: Martinez-Gimeno 2001 - M - Spain 11 - - - - retinal disease electroretinography: abolished rod and cone responses 1 1 LOVD
00409963 fam2pat1 PubMed: Martinez-Gimeno 2001 - M - Spain - - - - - retinal disease clinical symptoms of retinitis pigmentosa without electroretinographic responses 1 1 LOVD
00409965 fam5715(001-083)pat_II:2 PubMed: DeAngelis 2002 index patient F - - - - - - - retinal disease - 1 1 LOVD
00409966 fam5715(001-083)pat_III:2 PubMed: DeAngelis 2002 index patient's daughter 1 F - - - - - - - retinal disease age at onset of night blindness (years): 4, age at onset of visual field loss (years): 28; lens opacities (cataract) right/left eye: +/+; bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409967 fam5715(001-083)pat_III:3 PubMed: DeAngelis 2002 index patient's daughter 2 F - - - - - - - retinal disease no night blindness, age at onset of visual field loss (years): 13; lens opacities (cataract) right/left eye: -/-; bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409968 famE481 (001-338)pat_I:2 PubMed: DeAngelis 2002 index patient's paternal grandmother F - - - - - - - retinal disease - 1 1 LOVD
00409969 famE481 (001-338)pat_II:2 PubMed: DeAngelis 2002 index patient's father M - - - - - - - retinal disease - 1 1 LOVD
00409970 famE481 (001-338)pat_II:4 PubMed: DeAngelis 2002 index patient's paternal aunt F - - - - - - - retinal disease - 1 1 LOVD
00409971 famE481 (001-338)pat_III:1 PubMed: DeAngelis 2002 index patient M - - - - - - - retinal disease age at onset of night blindness (years): 5, age at onset of visual field loss (years): 16; lens opacities (cataract) right/left eye: -/-; bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409972 famE481 (001-338)pat_III:2 PubMed: DeAngelis 2002 index patient's brother M - - - - - - - retinal disease - 1 1 LOVD
00409973 fam5763 (001-122)pat_I:1 PubMed: DeAngelis 2002 index patient's father M - - - - - - - retinal disease - 1 1 LOVD
00409974 fam5763 (001-122)pat_II:3 PubMed: DeAngelis 2002 index patient M - - - - - - - retinal disease age at onset of night blindness (years): 1, age at onset of visual field loss (years): 12; lens opacities (cataract) right/left eye: +/-; bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409975 fam5677 (001-172)pat_I:2 PubMed: DeAngelis 2002 index patient's mother F - - - - - - - retinal disease age at onset of night blindness (years): 1, age at onset of visual field loss (years): 13; lens opacities (cataract) right/left eye: +/+ (removed right eye at age 45 years and in the left eye at age 65 years); bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409976 fam5677 (001-172)pat_II:2 PubMed: DeAngelis 2002 index patient F - - - - - - - retinal disease no night blindness, no visual field loss; lens opacities (cataract) right/left eye: -/-; bone-spicule pigment in at least 1 quadrant right/left eye: +/+ 1 1 LOVD
00409977 fam5677 (001-172)pat_III:2 PubMed: DeAngelis 2002 index patient's son M - - - - - - - retinal disease age at onset of night blindness (years): 2, no visual field loss; lens opacities (cataract) right/left eye: -/-; bone-spicule pigment in at least 1 quadrant right/left eye: +/- 1 1 LOVD
00409981 048-096 PubMed: Nishiguchi 2004 Family 1160 F - - - - - - - retinal disease best corrected visual acuity right, left eye: 20/200, 20/70; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: nondetectable; 30-Hz white right, left eye: nondetectable 1 1 LOVD
00409982 003-001 PubMed: Nishiguchi 2004 Family 7080, proband F - - - - - - - retinal disease clumped pigmentary retinal dystrophy; best corrected visual acuity right, left eye: 20/40, 20/40; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: 8, 6; 30-Hz white right, left eye: 0.9, 0.6 2 1 LOVD
00409983 078-059 PubMed: Nishiguchi 2004 - ? - - - - - - - retinal disease best corrected visual acuity right, left eye: 20/100, 20/200; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: 458, 396; 30-Hz white right, left eye: 37, 51 1 1 LOVD
00409984 003-252 PubMed: Nishiguchi 2004 - ? - - - - - - - retinal disease best corrected visual acuity right, left eye: 20/30, 20/30; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: 4, 4; 30-Hz white right, left eye: 0.8, 0.9 1 1 LOVD
00409985 115-031 PubMed: Nishiguchi 2004 Family J408 M - - - - - - - retinal disease father deceased, segregation impossible; best corrected visual acuity right, left eye: 20/100, 20/200; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: 308, 264; 30-Hz white right, left eye: 4, 5 1 1 LOVD
00409986 048-019 PubMed: Nishiguchi 2004 Family 1508 F - - - - - - - retinal disease best corrected visual acuity right, left eye: hand motions/hand motions; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: nondetectable; 30-Hz white right, left eye: 0.4, 0.5 1 1 LOVD
00409987 115-039 PubMed: Nishiguchi 2004 - ? - - - - - - - retinal disease best corrected visual acuity right, left eye: 20/200, 20/200; electroretinography amplitude, uV, 0.5-Hz white, right, left eye: 309, 212; 30-Hz white right, left eye: 39, 33 1 1 LOVD
00409988 003-001 PubMed: Nishiguchi 2004 Family 7080, brother of 003-001 M - - - - - - - retinal disease - 2 1 LOVD
00409990 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409991 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409992 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409993 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409994 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409995 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409996 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409997 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409998 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
00409999 ? PubMed: Kanda 2007 cell line (HEK) NRL protein investigation - - - - - - - - retinal disease - 1 1 LOVD
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