All individuals with variants in gene CNGB3

816 entries on 9 pages. Showing entries 1 - 100.
Legend   How to query   « First ‹ Prev     1 2 3 4 5 6 7 8 9     Next › Last »

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00095944 61036 PubMed: Li 2017 - F yes Pakistan Pakistani - - - - RD progressive RD 1 1 James Hejtmancik
00105013 71ORG1 PubMed: de Castro-Miró 2016 - F yes Saudi Arabia - - - - - ACHM - 1 1 Marta de Castro-Miró
00105022 22ORG1 PubMed: de Castro-Miró 2016 - F no Spain - - - - - retinal disease - 1 1 Marta de Castro-Miró
00144158 - PubMed: Katagiri 2014 index patient M no Japan Japanese - - - - retinal disease - 1 1 Rob W.J. Collin
00155440 - Sharon, submitted - F no Israel white;Jewish - - - - ACHM3 - 2 2 Dror Sharon
00155441 - Sharon, submitted - M no Israel African-N;Jewish - - - - ACHM3 - 1 1 Dror Sharon
00155442 - Sharon, submitted - M no Israel Jewish-Ashkenazi - - - - ACHM3 - 2 4 Dror Sharon
00155443 - Sharon, submitted - M no Israel white;Jewish - - - - ACHM3 - 1 1 Dror Sharon
00155444 - Sharon, submitted - M yes Israel beduin - - - - ACHM3 - 1 2 Dror Sharon
00155445 - Sharon, submitted - M no Israel Jewish-Ashkenazi - - - - ACHM3 - 1 2 Dror Sharon
00155446 - Sharon, submitted - F no Israel Jewish-Ashkenazi - - - - ACHM3 - 2 1 Dror Sharon
00170849 IRD4.0_#15 Manuscript under review (González-del Pozo et al., 2018) - M ? Spain - - - - - COD - 1 1 María González-del Pozo
00173732 10888875-Fam1 PubMed: Sundin 2000 large multi-generation family, 23 affected, unaffected heterozygous carrier relatives F;M - Micronesia Pingelapese islanders - - - - ACHM see paper; ..., total colorblindness, photophobia, nystagmus, 20/200 visual acuity, normal-appearing retina; ECG slightly lower than normal rod function, no detectable cone response 1 23 Johan den Dunnen
00173733 10888875-Fam2 PubMed: Sundin 2000 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no Micronesia Pingelapese islanders - - - - ACHM achromatopsia, total colourblindness, photophobia, nystagmus, 20/200 visual acuity, normal-appearing retina, healthy, normal intelligence; electroretinography older brother revealed normal rod response, no cone response 2 2 Johan den Dunnen
00173737 10888875-Fam3 PubMed: Sundin 2000 affected female F ? Micronesia Pingelapese islanders - - - - ACHM horizontal nystagmus, marked photophobia; normal electroretinographic rod response, no detectable cone response 1 1 Johan den Dunnen
00173738 10958649-FamCHRO4 PubMed: Kohl 2000 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - - white - - - - ACHM - 1 1 Johan den Dunnen
00173740 10958649-FamCHRO12 PubMed: Kohl 2000 2-generation family, 2 affected (2M), unaffected heterozygous carrier parents/relatives M - - white - - - - ACHM - 2 2 Johan den Dunnen
00173741 10958649-FamCHRO17 PubMed: Kohl 2000 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - - white - - - - ACHM - 2 1 Johan den Dunnen
00173742 10958649-FamCHRO19 PubMed: Kohl 2000 2-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives F;M - - white - - - - ACHM - 1 3 Johan den Dunnen
00173743 10958649-FamCHRO56 PubMed: Kohl 2000 2-generation family, 3 affected (3F), unaffected heterozygous carrier parents/relatives F - - white - - - - ACHM - 1 3 Johan den Dunnen
00173744 10958649-FamCHRO92 PubMed: Kohl 2000 2-generation family, 2 affected (2M), unaffected heterozygous carrier parents/relatives M - - white - - - - ACHM - 1 2 Johan den Dunnen
00173745 10958649-FamCHRO120 PubMed: Kohl 2000 2-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives F;M - - white - - - - ACHM - 1 2 Johan den Dunnen
00173746 10958649-FamCHRO182 PubMed: Kohl 2000 2-generation family, 3 affected (F, 2?), unaffected heterozygous carrier parents/relatives F - - white - - - - ACHM - 1 3 Johan den Dunnen
00173747 10958649-FamCHRO183 PubMed: Kohl 2000 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M - Micronesia - - - - - ACHM - 1 1 Johan den Dunnen
00173748 10958649-FamCHRO184 PubMed: Kohl 2000 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F - - white - - - - ACHM - 1 1 Johan den Dunnen
00263131 - - - F - - - - - - - ? Achromatopsia (HP:0011516) 1 1 IMGAG
00294669 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 130 Mohammed Faruq
00294670 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00294671 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294672 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 233 Mohammed Faruq
00294673 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 58 Mohammed Faruq
00295560 - - - F - - - - - - - ? Abnormal eye physiology (HP:0012373); Achromatopsia (HP:0011516) 1 1 Andreas Laner
00305204 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00305205 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 11 Mohammed Faruq
00305206 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00308499 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308500 - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309094 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309095 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00309096 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00309097 - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - retinal disease - 1 5 Global Variome, with Curator vacancy
00309098 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00309099 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309100 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309101 - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - retinal disease - 1 2 Global Variome, with Curator vacancy
00309102 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00309103 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00319828 FamDPatII1 PubMed: Eksandh 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Sweden - - - - - retinal disease Age: 2y 1 1 Julia Lopez
00319829 FamEPatII1 PubMed: Eksandh 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Sweden - - - - - retinal disease Age: 2y6m 1 1 Julia Lopez
00319830 FamFPatIII1 PubMed: Eksandh 2002 3-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives M - Sweden - - - - - retinal disease Age: 13y 1 4 Julia Lopez
00319831 FamFPatIII2 PubMed: Eksandh 2002 sister F - Sweden - - - - - retinal disease Age: 13y 1 1 Julia Lopez
00319832 FamFPatIII3 PubMed: Eksandh 2002 nephew M - Sweden - - - - - retinal disease Age: 21y 1 1 Julia Lopez
00319833 FamGPatII1 PubMed: Eksandh 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Sweden - - - - - retinal disease Age: 26y 1 1 Julia Lopez
00319834 FamHPatII1 PubMed: Eksandh 2002 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Sweden - - - - - retinal disease Age: 36y 2 1 Julia Lopez
00320042 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 10y 2 1 Julia Lopez
00320043 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 8y 2 1 Julia Lopez
00320044 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 38y 1 1 Julia Lopez
00320048 - PubMed: Johnson 2004 2nd variant not found. Probably out of the screening scope. - - United Kingdom (Great Britain) - - - - - retinal disease age: 44y 1 1 Julia Lopez
00320054 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 14y 1 1 Julia Lopez
00320055 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 20y 1 1 Julia Lopez
00320057 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 34y 1 1 Julia Lopez
00320058 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 36y 2 1 Julia Lopez
00320060 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 2y 1 1 Julia Lopez
00320061 - PubMed: Johnson 2004 - - - United Kingdom (Great Britain) - - - - - retinal disease age: 24y 1 1 Julia Lopez
00320063 - PubMed: Johnson 2004 2nd variant not found. Probably out of the screening scope. - - United Kingdom (Great Britain) - - - - - retinal disease age: 12y 1 1 Julia Lopez
00324248 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 2 1 Julia Lopez
00324251 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 2 1 Julia Lopez
00324255 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324256 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324258 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324259 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324262 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324263 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324264 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 2 1 Julia Lopez
00324266 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324268 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324269 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324271 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 2 1 Julia Lopez
00324272 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324273 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324274 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00324275 - PubMed: Nishiguchi 2005 - - - - - - - - - retinal disease - 1 1 Julia Lopez
00325487 3580 PubMed: Zenteno 2020 single patient - - Mexico - - - - - retinal disease retinitis pigmentosa 1 1 Johan den Dunnen
00327935 B240061 PubMed: Carss 2017 - M - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00327967 B240280 PubMed: Carss 2017 - M - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00328023 G001290 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328135 G005509 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328206 G007720 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328311 W000192 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00328338 W000373 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00328451 14000069 PubMed: Taylor 2017 no family history retinal disease M - United Kingdom (Great Britain) - - - - - retinal disease cone dysfunction syndrome (HP:0030637) 2 1 LOVD
00328452 15003158 PubMed: Taylor 2017 no family history retinal disease F - United Kingdom (Great Britain) - - - - - retinal disease cone dysfunction syndrome (HP:0030637) 1 1 LOVD
00328453 86795 PubMed: Taylor 2017 no family history retinal disease M - United Kingdom (Great Britain) - - - - - retinal disease cone dysfunction syndrome (HP:0030637) 2 1 LOVD
00328454 14012482 PubMed: Taylor 2017 no family history retinal disease F - United Kingdom (Great Britain) - - - - - retinal disease cone dysfunction syndrome(HP:0030637), cone/cone-rod dystrophy (HP:0000548) 2 1 LOVD
00331296 Fam12 PubMed: Wawrocka 2018 - - - Poland - - - - - retinal disease - 1 1 LOVD
00331299 Fam6 PubMed: Wawrocka 2018 - - - Poland - - - - - retinal disease - 1 1 LOVD
00331720 Pat9 PubMed: Matet 2018 - F yes - white - - - - retinal disease see paper; ..., detailed analysis 1 1 LOVD
00331721 Pat10 PubMed: Matet 2018 - F yes - Africa-North - - - - retinal disease see paper; ..., detailed analysis 1 1 LOVD
00331722 Pat11 PubMed: Matet 2018 - F no - white - - - - retinal disease see paper; ..., detailed analysis 2 1 LOVD
00331723 ?;Pat12 PubMed: Mayer 2017, PubMed: Matet 2018 - M no - white - - - - retinal disease see paper; ..., detailed analysis 1 1 LOVD
Legend   How to query   « First ‹ Prev     1 2 3 4 5 6 7 8 9     Next › Last »


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.