All individuals with variants in gene PXDN

20 entries on 1 page. Showing entries 1 - 20.
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00011670 - - - - - - - - - - - ? - 1 1 Anne Slavotinek
00016311 - - - - - - - - - - - - - 2 1 Anne Slavotinek
00016312 - - - F no - - - - - - ? - 2 1 Anne Slavotinek
00016314 - - - - - - - - - - - CTRCT - 2 1 Anne Slavotinek
00150101 - - - M yes - - - - - - microcephaly, postnatal progressive, with seizures and brain atrophy - 1 1 Celia Zazo-Seco
00150102 - - - M no - - - - - - - - 2 1 Celia Zazo-Seco
00151411 - - - F no - - - - - - MCOP microphthalmia (HP:0000568) 1 1 Celia Zazo-Seco
00292303 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 71 Mohammed Faruq
00292304 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00292305 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 11 Mohammed Faruq
00332116 F44‐M PubMed: Patel 2017 family - - Saudi Arabia - - - - - MCOP - 1 1 LOVD
00332117 F45‐M PubMed: Patel 2017 family - yes Saudi Arabia - - - - - MCOP - 1 1 LOVD
00390062 Pat9 PubMed: Kritioti 2021 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes Cyprus Greece - - - - ? Bilateral iris defects, extensive anterior synechiae, posterior embryotoxon, nystagmus, glaucoma, cataracts, bilateral hydronephrosis, vesicoureteric obstruction, bilateral megaureter and bipolar disorder 1 1 Johan den Dunnen
00434859 CMC48 PubMed: Gostain 2020 - F - Canada - - - - - ? microphthalmia, sclerocornea, Peters anomaly, aphakia, intrauterine growth retardation, seizures, unilateral renal dysplasia, hemihypertrophy lower limb 2 1 Johan den Dunnen
00440086 MA144PatV4 PubMed: Basharat 2023, Journal: Basharat 2023 5-generation family, 3 affected sibs (F, 2M), unaffected heterozygous parents/relatives M yes Pakistan Asia-S - - - - ? see paper; ..., anterior segment dysgenesis 1 3 Rabia Basharat
00440088 MA193PatIV2 PubMed: Basharat 2023, Journal: Basharat 2023 4-generation family, affected brother/sister (F, M), unaffected heterozygous parents/relatives F yes Pakistan Asia-S - - - - ? see paper; ... 1 2 Rabia Basharat
00444909 Fam26PatII4 PubMed: Ma 2016 3-generation family, 6 affected (6M) M - Australia - - - - - CTRCT see paper; ..., bilateral lamellar cataract 1 6 Johan den Dunnen
00444946 10DG1905 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT congenital cataract with peters anomaly; not syndromic 1 1 Johan den Dunnen
00445071 ASGD00884 PubMed: Kessel 2021 patient - - Denmark - - - - - CTRCT Peters anomaly 2 1 Johan den Dunnen
00469934 Fam8PatII1 PubMed: Thanikachalam 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents M - United States white;non-Hispanic - - - - ASGD see paper; ..., bilateral Peters anomaly 2 1 Johan den Dunnen
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