Full data view for gene RDH5

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_002905.3 transcript reference sequence.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

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AscendingDNA change (cDNA)     

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DNA change (genomic) (hg19)     

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+?/? 4 c.712G>T r.(?) p.(Gly238Trp) Parent #2 - likely pathogenic g.56117812G>T g.55724028G>T - - RDH5_000004 Compound heterozygous missense mutation PubMed: Schatz 2010 - - Germline - - - - - DNA PCR, SEQ - - fundus albipunctatus (retinitis punctata albescens (RPA)) - PubMed: Schatz 2010 ? M no Germany German - - - - 1 Raheel Qamar
+/. - c.712G>T r.(?) p.(Gly238Trp) Unknown - pathogenic g.56117812G>T g.55724028G>T RDH5(NM_001199771.1):c.712G>T (p.G238W) - RDH5_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.712G>T r.(?) p.(Gly238Trp) Unknown ACMG pathogenic g.56117812G>T - - - RDH5_000004 - PubMed: Sharon 2019 - - Germline - 4/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 4 IRD families - - Israel - - - - - 4 Global Variome, with Curator vacancy
+?/. 4 c.712G>T r.(?) p.(Gly238Trp) Unknown - likely pathogenic g.56117812G>T g.55724028G>T RDH5 Ex.4 c.712G>T p.(Gly238Trp), Ex.4 c.572G>A p.(Arg191Gln) - RDH5_000004 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-2025 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. - c.712G>T r.(?) p.(Gly238Trp) Unknown - likely pathogenic g.56117812G>T g.55724028G>T RDH5 c.712G>T - RDH5_000004 no protein change given, heterozygous PubMed: Zanolli 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 9 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - 1 LOVD
+?/. - c.712G>T r.(?) p.(Gly238Trp) Parent #1 - likely pathogenic g.56117812G>T g.55724028G>T RDH5, variant 1: c.712G>T/p.G238W, variant 2: c.712G>T/p.G238W - RDH5_000004 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 637 PubMed: Weisschuh 2020 Filing key number: 227, unclassified / mixed, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.712G>T r.(?) p.(Gly238Trp) Both (homozygous) - likely pathogenic (recessive) g.56117812G>T g.55724028G>T RDH5 G238W - RDH5_000004 expresion levels (% wild type): 2; in vivo activity (% wild type): <1; in vitro activity: non-active; expected consequences and localisation of mutations: W238 is bulky and located at the subunit interface and may affect subunit interactions; no nucleotide annotation, extrapolated from protein PubMed: Liden 2001 - - In vitro (cloned) ? - - - - DNA ? - in vitro assays retinal disease ? PubMed: Liden 2001 protein expression and enzymatic activity of naturally occurring RDH5 mutants in COS-1 cells - - - - - - - - 1 LOVD
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