All individuals with variants in gene AP5Z1

22 entries on 1 page. Showing entries 1 - 22.
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00294469 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 127 Mohammed Faruq
00294470 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 200 Mohammed Faruq
00305165 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00305166 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00311035 - - - M - - - - - - - ? Abnormality of central motor function (HP:0011442); Abdominal symptom (HP:0011458); Ataxia (HP:0001251); Episodic vomiting (HP:0002572) 2 1 Andreas Laner
00464709 Fam1Pat1 PubMed: Kaminska 2025 3-generation family, 3 affected brothers, unaffected heterozygous carrier parents M - Portugal - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; pollakiuria 2 3 Johan den Dunnen
00464710 Fam1Pat2 PubMed: Kaminska 2025 brother M - Portugal - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; peripheral neuropathy with paraplegia 2 1 Johan den Dunnen
00464711 Fam1Pat3 PubMed: Kaminska 2025 brother M - United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; blurred vision; extensive central chorioretinal atrophy; no neurological symptoms; 50y-hearing loss 2 1 Johan den Dunnen
00464712 Fam2Pat4 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - Belgium - - - - - macular dystrophy macular dystrophy; unilateral central vision loss, central scotoma, paresthesia; extensive central chorioretinal atrophy; paresthesia in hands and feet, mild intellectual disability, ataxic gait; impression of hearing loss 2 1 Johan den Dunnen
00464713 Fam3Pat5 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - Israel - - - - - macular dystrophy macular dystrophy; reduced visual acuity; maculopathy with atrophy and deposits; no neurological symptoms; 40y-hearing loss 1 1 Johan den Dunnen
00464714 Fam4Pat6 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents F - Israel - - - - - macular dystrophy macular dystrophy; reduced visual acuity; maculopathy with atrophy; no neurological symptoms 2 1 Johan den Dunnen
00464715 Fam5Pat7 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M yes United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; pollakiuria; 35y-neurosensory hearing loss; hypercholesterolemia; hypertension; asthma 1 1 Johan den Dunnen
00464716 Fam6Pat8 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; mostly asymptomatic; extensive central chorioretinal atrophy; no neurological symptoms 1 1 Johan den Dunnen
00464717 Fam7Pat9 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; no neurological symptoms; hypertension; >50y-hearing loss 2 1 Johan den Dunnen
00464718 Fam8Pat10 PubMed: Kaminska 2025 2-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents M - United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; no neurological symptoms 2 2 Johan den Dunnen
00464719 Fam8Pat11 PubMed: Kaminska 2025 sister F - United Kingdom (Great Britain) - - - - - macular dystrophy macular dystrophy; central vision loss; extensive central chorioretinal atrophy; no neurological symptoms; hiatus hernia; diverticulosis and colitis; hypertension; bilateral sensorineural hearing loss (onset late 50s) 2 1 Johan den Dunnen
00464720 Fam9Pat12 PubMed: Kaminska 2025 3-generation family, 1 affected, unaffected heterozygous carrier parents M - Spain - - - - - macular dystrophy macular dystrophy; nyctalopia, reduced visual acuity; extensive central chorioretinal atrophy; no neurological symptoms; impression of hearing loss in left ear; hypertension; type 2 diabetes 1 1 Johan den Dunnen
00464721 Fam10Pat13 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Sweden - - - - - macular dystrophy macular dystrophy; problem with reading; extensive central chorioretinal atrophy; no neurological symptoms 2 1 Johan den Dunnen
00464722 Fam11Pat14 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Germany - - - - - macular dystrophy macular dystrophy; metamorphopsias; early maculopathy with deposits; no neurological symptoms; thyroid dysfunction 2 1 Johan den Dunnen
00464723 Fam12Pat15 PubMed: Kaminska 2025 2-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents M - Germany - - - - - macular dystrophy macular dystrophy; poor central vision; extensive central chorioretinal atrophy; parkinsonism 1 1 Johan den Dunnen
00464724 Fam13Pat16 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Switzerland - - - - - macular dystrophy macular dystrophy; spastic atactic gait; early maculopathy; spastic atactic paraparesis 1 1 Johan den Dunnen
00464725 Fam14Pat17 PubMed: Kaminska 2025 2-generation family, 1 affected, unaffected heterozygous carrier parents F yes Spain - - - - - macular dystrophy macular dystrophy; paresthesia; early maculopathy with deposits; paresthesia in the right hand 1 1 Johan den Dunnen
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