All individuals with variants in gene AGBL5

45 entries on 1 page. Showing entries 1 - 45.
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00232190 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232191 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232192 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232193 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232194 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232195 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232196 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00232197 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232198 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232199 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232200 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232201 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232202 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232203 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 4 Yoshito Koyanagi
00232204 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 3 Yoshito Koyanagi
00232205 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232206 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232207 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232208 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232209 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232210 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232211 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232212 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232213 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232214 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232215 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 9 Yoshito Koyanagi
00232216 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 3 Yoshito Koyanagi
00232217 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232218 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00276087 FamE PubMed: Kastner 2015 2-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents - yes Turkey - - - - - retinal disease see paper; ... 1 3 Johan den Dunnen
00308937 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00363757 12DG0507 PubMed: Patel 2016 2-generation family, 3 affected brothers, unaffected heterozygous carrier parents/relatives M - - - - - - - retinal disease see paper; ... 1 3 Johan den Dunnen
00383407 - PubMed: Khan 2019 - F - - - - - - - retinal disease - 1 1 LOVD
00383872 MOL1514 III:4 PubMed: Abu Diab 2019 Mixed Arabic Muslim and Christian descent F yes Israel - - - - - retinal disease RP and liver dysfunction 1 1 LOVD
00387387 7 PubMed: Sun 2020 - F - China - - - - - retinal disease no lens opacity, no choroidal atrophy, negative family history, BCVA OD/OS: 0.6/0.8, retinal crystal deposit 2 1 LOVD
00390160 G007663 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
00391362 18 {PMID:Méjécase 2020:3278337 - ? - United Arab Emirates - - - - - retinal disease - 1 1 LOVD
00392261 7 PubMed: Bell 2021 - F yes (United Kingdom (Great Britain)) - - - - - retinal disease Posterior subcapsular cataract,retinal dystrophy, macular oedema 1 1 LOVD
00408725 II:3 PubMed: Branham 2016 - F - - - - - - - retinal disease 11y: several-year history of nyctalopia; best corrected visual acuity: 20/20 both eyes; visual field: unreliable; electroretinography: barely recordable responses both eyes; fundus: early optic nerve pallor and surface gliosis, vascular attenuation, depressed foveal reflex, fine retinal pigment epithelium granularityl peripheral retina: a few areas of bone spicule-like pigmentation and a coarse retinal pigment epithelium granularity. 17y: best corrected visual acuity: 20/30 both eyes, visual fields:constricted. 24y: best corrected visual acuity right, left eye: 20/50, 20/30; greatly constricted visual field; fundus: heavy bone spicule pigmentation in the equatorial region both eyes; medical history: petit mal seizures beginning at the age of 8 yr, controlled with medication 2 1 LOVD
00408726 II:2 PubMed: Branham 2016 - M - - - - - - - retinal disease 15y: history of impaired night vision; best corrected visual acuity right, left eye: 20/15, 20/20 left eye; visual field: full fields with the v4e isopter, but constriction to 30 degrees centrally with the i4e isopter; . electroretinography: scotopic barely recordable, photopic responses 50% reduction of amplitude and normal waveform; fundus: slight optic disc pallor and gliosis; attenuated vessels; foveal reflex intact in both eyes, retinal pigment epithelium intact in both maculae; peripheral retina: fine bone spicule pigmentation and fine granularity to the retinal pigment epithelium 2 1 LOVD
00408727 F1-IV:3 PubMed: Astuti 2016 Family 1, individual IV:3 M - - - - - - - retinal disease best corrected visual acuity right, left eye: light perception, no light perception; ophthalmoscopy: mild optic disk pallor, attenuated vessels, macular and (mid-) peripheral retinal pigment epithelium atrophy with heavy intraretinal bone spicule pigmentations and deep nummular pigmentations; full field electroretinography: not available; optical coherence tomography: cystoid maculopathy progressing into complete loss of outer retinal layers and thinning inner retinal layers at fovea; fundus autofluorescence: not performed; other symptoms: pseudophakia, cataract extraction (age 29), band keratopathy, cystoid macular edema (responsive to subcutaneous octreotide), Morbus Behcet 1 1 LOVD
00408728 F2-II:1 PubMed: Astuti 2016 Family 2, individual II:1 F - - - - - - - retinal disease best corrected visual acuity right, left eye: 6/18 (0.48), 6/12 (0.3); ophthalmoscopy: optic disc pallor, attenuated vessels, macular and midperipheral retinal pigment epithelium mottling and occasional hyperpigmented spots; full field electroretinography: 8y, findings of marked rod system dysfunction with cone system dysfunction right eye>left eye; marked macular involvement right eye; optical coherence tomography: cysts in inner nuclear layer right eye<left eye, centrally preserved inner segment ellipsoid band and outer nuclear layers right eye<left eye; fundus autofluorescence: parafoveal hyper-autofluorescent ring larger on left eye, right eye additional ring of hypoautofluorescence surrounding this in macula, midperipheral spots of hypo-autofluorescence; other symptoms: posterior subcapsular cataract, cystoid macular ed ma (responsive to topica carbonic anhydrase inhibitor), right amblyopia, right secondary exotropia 2 1 LOVD
00408729 F2-II:3 PubMed: Astuti 2016 Family 2, individual II:3 F - - - - - - - retinal disease best corrected visual acuity right, left eye: 6/18 (0.48), 6/18 (0.48); ophthalmoscopy: optic disc pallor, attenuated vessels, macular and midperipheral retinal pigment epithelium mottling, minimal pigment spots; full field electroretinography: 20y, severe generalized loss of retinal function; optical coherence tomography: cysts inner nuclear layer, small foveal region of preserved inner segment ellipsoid band; fundus autofluorescence: foveal hyper-autofluorescence surrounded by parafoveal hypo-autofluorescent ring, midperipheral spots of hypo-autofluorescence; other symptoms: posterior subcapsular cataract, cystoid macular ed ma (responsive to carbonic anhydrase inhibitor), learning difficulties 2 1 LOVD
00408730 F3-II:1 PubMed: Astuti 2016 Family 3, individual II:1 F - - - - - - - retinal disease best corrected visual acuity right, left eye: 6/12 (0.3), 6/12 (0.3); ophthalmoscopy: optic disc pallor, attenuated vessels, macular retinal pigment epithelium mottling, heavy midperipheral bone spicule pigmentation; full field electroretinography: 39y, findings consistent with RP, report not available ; optical coherence tomography: cysts in inner nuclear layer, centrally preserved outer nuclear layer and inner segment ellipsoid band (disrupted), epiretinal membrane ; fundus autofluorescence: parafoveal spots of hypo-autofluorescence, extensive speckled midperipheral loss of autofluorescence; other symptoms: cataract, cystoid macular edema (responsive to carbonic anhydrase inhibitor) 2 1 LOVD
00426944 48_57 PubMed: Zhu 2022 family 48, individual 57 F - - - - - - - retinal disease - 1 1 LOVD
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