All individuals with variants in gene KIAA0586

23 entries on 1 page. Showing entries 1 - 23.
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00183256 29446546-Pat1 PubMed: Pinz 2018 2-generation family, 1 affected, unaffected non-carrier parents M no United States - - - - - ? see paper; ..., 2 1 Johan den Dunnen
00291064 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291065 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 82 Mohammed Faruq
00304432 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00307148 Pat6 PubMed: Krygier 2019 family, 2 affected brothers M - Poland - - - - - ataxia pyramidal signs, abnormal sleep‐wake rhythm, vertical supranuclear gaze palsy, hepatosplenomegaly, elevated serum levels of cholesterol, uric acid and aminotransferases, mild cognitive decline; MRI brain generalized cortical and subcortical atrophy, cerebellar atrophy 2 1 Johan den Dunnen
00377660 443 PubMed: Brooks 2018 family 51 F - United States - - - - - retinal disease oculomotor apraxia, strabismus, retinal degeneration, vessel attenuation, optic nerve atrophy 1 1 LOVD
00377661 368 PubMed: Brooks 2018 family 52 M - United States - - - - - retinal disease strabismus, coloboma - retina, retinal degeneration, optic nerve atrophy 2 1 LOVD
00377662 494 PubMed: Brooks 2018 family 53 M - United States - - - - - retinal disease oculomotor apraxia, coloboma - retina 2 1 LOVD
00377663 579p PubMed: Brooks 2018 family 54 M - United States - - - - - retinal disease oculomotor apraxia 2 1 LOVD
00377664 507 PubMed: Brooks 2018 family 55 M - United States - - - - - retinal disease oculomotor apraxia, nystagmus, strabismus, optic nerve atrophy 2 1 LOVD
00377665 531p PubMed: Brooks 2018 family 56 M - United States - - - - - retinal disease optic nerve atrophy 2 1 LOVD
00386932 FamAPatIII1(Pat19) PubMed: Chen 2017 family, proband and 2 affected sibs, unaffected parents M - Netherlands - - - - - SLI see paper; ..., all affected specific language impairment, special educational needs 2 1 Johan den Dunnen
00388078 368 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00388088 443 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00388104 494 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00388109 507 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00388118 531 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00388138 579 PubMed: Summers 2017 - - - United States - - - - - retinal disease - 2 1 LOVD
00435047 - - - - - France - - - - - JBTS23 - 2 1 Svetlana Gorokhova
00465292 COR62 PubMed: D'Abrusco 2025, Journal: D'Abrusco 2025 - - - - - - - - - JBTS - 2 1 Johan den Dunnen
00465293 COR164 PubMed: D'Abrusco 2025, Journal: D'Abrusco 2025 - - - - - - - - - JBTS - 2 1 Johan den Dunnen
00465294 COR93 PubMed: D'Abrusco 2025, Journal: D'Abrusco 2025 - - - - - - - - - JBTS - 2 1 Johan den Dunnen
00465295 COR130 PubMed: D'Abrusco 2025, Journal: D'Abrusco 2025 - - - - - - - - - JBTS - 2 1 Johan den Dunnen
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