All individuals with variants in gene GRM6

90 entries on 1 page. Showing entries 1 - 90.
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00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 1 1 Yu Sun
00059923 - - 1 familie M yes India Indian - - - - CSNB1B - 1 1 Soumittra Nagasamy
00100090 61155 PubMed: Li 2017 - F yes Pakistan Pakistani - - - - CSNB - 1 1 James Hejtmancik
00100095 61170 PubMed: Li 2017 - M yes Pakistan Pakistani - - - - CSNB - 1 1 James Hejtmancik
00100096 61172 PubMed: Li 2017 - M yes Pakistan Pakistani - - - - CSNB - 1 1 James Hejtmancik
00144156 - PubMed: Katagiri 2014 index patient F no Japan Japanese - - - - retinal disease - 1 1 Rob W.J. Collin
00293824 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 162 Mohammed Faruq
00293825 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00293826 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 120 Mohammed Faruq
00293827 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 68 Mohammed Faruq
00305026 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00305027 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00305028 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00308708 - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - Healthy/Control - 1 1 Global Variome, with Curator vacancy
00327461 M68 II-1 Doucette 2021, submitted Only Affected brother of a 4 member family. 1 unaffected sister and unaffected parents. Patient has an occult macular dystrophy though no RP1L1 variants were noted. M - Canada - - - Yes - maculopathy Fundus: No specific findings OCT: Normal ERG:Central loss on multi-focal electroretinogram (abnormal ERG HP:0000512) - Reduced Visual Acuity 20/40 OU (HP:0007663) 1 1 Lance P Doucette
00328055 G001436 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 2 1 LOVD
00328294 W000165 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - retinal disease - 1 1 LOVD
00328474 15020397 PubMed: Taylor 2017 no family history retinal disease M - United Kingdom (Great Britain) - - - - - retinal disease congenital stationary night blindness (HP:0007642) 1 1 LOVD
00333353 Pat9 PubMed: Costa 2017 - F - Brazil - - - - - retinal disease see paper; ... 1 1 LOVD
00333364 Pat4 PubMed: Costa 2017 - F - Brazil - - - - - retinal disease see paper; ... 1 1 LOVD
00334966 H33 PubMed: Jin 2017 - - - China - - - - - ? see paper; ... 1 1 LOVD
00358958 Case71471 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358971 Case70946 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00358972 Case70559 PubMed: Tiwari 2016 see paper M - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00362232 Pat14 PubMed: Fadaie 2021 - F - Netherlands - - - - - retinal disease - 2 1 Zeinab Fadaie
00363458 UFC+7.74 PubMed: Ge 2015 simplex case - - United States - - - - - retinal disease see paper; ... 2 1 LOVD
00375386 - PubMed: Zeitz 2015 - - - Belgium - - - - - retinal disease see paper; ... 1 1 LOVD
00375387 - PubMed: Zeitz 2015 - - - United Kingdom (Great Britain) - - - - - retinal disease see paper; ... 1 1 LOVD
00376554 - PubMed: Zeitz-2009 - - - Germany - - - - - retinal disease - 1 1 LOVD
00376598 - PubMed: Zeitz-2009 SNP or modifier - - Switzerland - - - - - retinal disease - 1 1 LOVD
00376637 - PubMed: Zeitz-2009 - - - Netherlands - - - - - retinal disease - 1 1 LOVD
00376638 - PubMed: Zeitz-2009 - - - Netherlands - - - - - retinal disease - 1 1 LOVD
00376639 - PubMed: Zeitz-2009 - - - - - - - - - retinal disease - 1 1 LOVD
00376640 - PubMed: Zeitz-2009 - - - - - - - - - retinal disease - 1 1 LOVD
00376641 - PubMed: Zeitz-2009 SNP or modifier - - Germany - - - - - retinal disease - 1 1 LOVD
00376642 - PubMed: Zeitz-2009 - - - Germany - - - - - retinal disease - 1 1 LOVD
00376643 - PubMed: Zeitz-2009 - - - Netherlands - - - - - retinal disease - 1 1 LOVD
00376644 - PubMed: Zeitz-2009 - - - - - - - - - retinal disease - 1 1 LOVD
00376645 - PubMed: Zeitz-2009 - F - Germany - - - - - retinal disease - 1 1 LOVD
00376646 - PubMed: Zeitz-2009 - - - - - - - - - retinal disease - 1 1 LOVD
00376647 - PubMed: Zeitz-2009 - - - - - - - - - retinal disease - 1 1 LOVD
00376853 Pat8 PubMed: Malaichamy 2014 see paper - - India - - - - - retinal disease see paper; ... 1 1 LOVD
00379599 - PubMed: Wang-2012 - F - China - - - - - retinal disease - 1 1 LOVD
00379600 - PubMed: Wang-2012 - F - China - - - - - retinal disease - 1 1 LOVD
00379630 - PubMed: Godara-2012 - F - - - - - - - retinal disease - 2 1 LOVD
00379631 - PubMed: Godara-2012 - F - - - - - - - retinal disease - 2 1 LOVD
00379632 - PubMed: Godara-2012 - F - - - - - - - retinal disease - 2 1 LOVD
00381254 - PubMed: Bijveld-2013 - F - Netherlands Dutch - - - - retinal disease - 2 2 Julia Lopez
00381255 - PubMed: Bijveld-2013 - M - Netherlands Dutch - - - - retinal disease - 2 1 Julia Lopez
00381256 - PubMed: Bijveld-2013 - M - Netherlands Dutch - - - - retinal disease - 1 1 Julia Lopez
00382310 139 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 2 1 LOVD
00382550 412 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 2 1 LOVD
00384145 RP-2633 PubMed: Martin Merida 2019 - ? - Spain - - - - - retinal disease - 2 1 LOVD
00384234 12110 PubMed: Wang 2019 - M - China - - - - - retinal disease - 2 1 LOVD
00384287 13427 PubMed: Wang 2019 - M - China - - - - - MYP2 - 1 1 LOVD
00384384 14128 PubMed: Wang 2019 - F - China - - - - - retinal disease - 1 1 LOVD
00386875 121-056 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
00386907 OGI678_001361 PubMed: Zampaglione 2020 - ? - - - - - - - retinal disease - 1 1 LOVD
00388497 14016318 PubMed: Ellingsford 2018 - - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00389067 351 PubMed: Weisschuh 2020 Filing key number: 118, congenital stationary night blindness, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 2 1 LOVD
00390273 G001436 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
00390274 W000165 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - retinal disease - 1 1 LOVD
00415086 - - 3 generation family, parents unaffected heterozygous carriers F yes India Asian >18y - yes none CSNB - 1 1 Srilekha Sundar
00415087 - - - F no India Asian >05y - yes none CSNB - 1 1 Srilekha Sundar
00415564 274-011 PubMed: Dryja 2005 - M - (United States) - - - - - retinal disease Refractive error -0.25; VA(OD;OS): 20/20;20/20 1 1 LOVD
00415565 063-007 PubMed: Dryja 2005 - M - (United States) - - - - - retinal disease Refractive error -4.62; VA(OD;OS): 20/40;20/40 2 1 LOVD
00415566 274-021 PubMed: Dryja 2005 - F - (United States) - - - - - retinal disease Refractive error -5.38; VA(OD;OS): 20/25;20/30 1 1 LOVD
00415567 - PubMed: O'Connor 2006 - F - (United Kingdom (Great Britain)) - - - - - retinal disease poor night vision and horizontal nystagmus since early infancy; myopic astigmatism 1 1 LOVD
00415568 Subject 1 PubMed: Sergouniotis 2012 - M - - - - - - - retinal disease Refractive error: OD(-16.50?-1.00x110) - OS(-17); VA: OD(0.36) - OS(3); nystagmus 2 1 LOVD
00415569 Subject 2 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-12.00?-2.00x7) - OS(-11.00?-2.00x150); VA: OD(1.78*) - OS(0.80*); nystagmus 2 1 LOVD
00415570 Subject 3 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-1.00?-1.25x105) - OS(-0.50?-2.50x50); VA: OD(0.18*) - OS(0.18*) 1 1 LOVD
00415571 Subject 4 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-0.50?-1.00x80) - OS(-0.50?-1.50x105); VA: OD(0.2) - OS(0); nystagmus 1 1 LOVD
00415572 Subject 5 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-7.00?-3.50x10) - OS(-7.00?-1.75x175); VA: OD(0.20*) - OS(0.18*) 1 1 LOVD
00415573 Subject 6 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-4.50?-2.75x20) - OS(-6.00?-2.00x180); VA: OD(0.08) - OS(0.14) 1 1 LOVD
00415574 Subject 7 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(-3.50?-3.50x180) - OS(-3.50?-4.00x180); VA: OD(0.58) - OS(0.28); nystagmus 2 1 LOVD
00415575 Subject 8 PubMed: Sergouniotis 2012 - M - - - - - - - retinal disease Refractive error: OD(-4.25?-1.50x175) - OS(-2.50?-1.00x180); VA: OD(0.54) - OS(0.2) 1 1 LOVD
00415576 Subject 9 PubMed: Sergouniotis 2012 - F - - - - - - - retinal disease Refractive error: OD(+0.25?-0.75x25) - OS(+0.25?-1.50x160); VA: OD(0.22) - OS(0.2); nystagmus 2 1 LOVD
00415577 14 PubMed: Naeem-2015 - M yes - pakistani - - - - retinal disease VA: 6/60OD -6/60OS 1 1 LOVD
00415578 16 PubMed: Naeem-2015 - M yes - pakistani - - - - retinal disease VA: 6/6OD - 6/6OS; astigmatism/ hyperopia 1 1 LOVD
00415579 14 PubMed: Naeem-2015 - M yes - pakistani - - - - retinal disease VA: 6/9OD - 6/12OS; astigmatism/ hyperopia 1 1 LOVD
00415580 18 PubMed: Naeem-2015 - F yes - pakistani - - - - retinal disease VA: counting fingers 1 1 LOVD
00415581 19 PubMed: Naeem-2015 - F yes - pakistani - - - - retinal disease VA: counting fingers 1 1 LOVD
00415582 10 PubMed: Naeem-2015 - F yes - pakistani - - - - retinal disease VA: 6/36OD - counting fingers OS 1 1 LOVD
00415583 15 PubMed: Naeem-2015 - M yes - pakistani - - - - retinal disease VA: 6/6OD - 6/6OS; hyperopia 1 1 LOVD
00415584 II-2 PubMed: Tourville-2019 - F yes - - - - - - retinal disease Her visual acuity reached 9/10 for the right eye with -1.75(-1.75 at 155°) and 10/10 for the left eye with -2.75(-1.5 at 20°). (see paper) 1 1 LOVD
00415585 II-1 PubMed: Tourville-2019 - M yes - - - - - - retinal disease myopia and astigmatism but also a small angle esotropia with a moderate left eye amblyopia at 3/10. The cycloplegic refraction was ?1.75 (?1.75 at 155°) for the right eye and ?2.75 (?1.50 et 20°) for the left eye 1 1 LOVD
00415586 II3 PubMed: Liu-2019 - M - - - - - - - retinal disease Pseudodominant inheritance; mild myopia (?1.0 to ?2.0 D) with mild astigmatism; nystagmus and strabismus 2 1 LOVD
00415587 III3 PubMed: Liu-2019 - F - - - - - - - retinal disease Pseudodominant inheritance; mild myopia (?1.0 to ?2.0 D) with mild astigmatism; amblyopia 3 1 LOVD
00415588 III4 PubMed: Liu-2019 - M - - - - - - - retinal disease Pseudodominant inheritance; mild myopia (?1.0 to ?2.0 D) with mild astigmatism; amblyopia 3 1 LOVD
00435099 Fam_17_GRM6 - Heterozygous carrier parents M no India Asian >30y - Yes - CSNB - 1 1 Srilekha Sundar
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