Full data view for gene CERKL


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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Owner     
+/. - c.481+2T>G r.spl? p.? Unknown - pathogenic g.182468562A>C g.181603835A>C - - CERKL_000026 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.481+2T>G r.spl p.? Both (homozygous) - VUS g.182468562A>C g.181603835A>C IVS2+2T>G - CERKL_000026 - PubMed: Wang 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - 184-gene panel retinal disease RD12–06 PubMed: Wang 2017 - - - United States - - - - - 1 LOVD
+?/. - c.481+2T>G r.spl p.(?) Both (homozygous) ACMG likely pathogenic g.182468562A>C g.181603835A>C CERKL c.481+2T>G, p.(?), c.481+2T>G, p.(?) - CERKL_000026 homozygous PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 78 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.481+2T>G r.spl p.(?) Parent #1 - likely pathogenic g.182468562A>C g.181603835A>C CERKL, variant 1: c.481+2T>G/p.?, variant 2: c.481+2T>G/p.? - CERKL_000026 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 994 PubMed: Weisschuh 2020 Filing key number: 458, cone-rod dystrophy, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.481+2T>G r.spl p.(?) Parent #1 - likely pathogenic g.182468562A>C g.181603835A>C CERKL, variant 1: c.481+2T>G/p.?, variant 2: c.1642T>G/p.Y548D - CERKL_000026 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET9 targeted sequencing panel - see paper retinal disease 1108 PubMed: Weisschuh 2020 Filing key number: 749, cone-rod dystrophy, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. 2i c.481+2T>G r.spl? p.(?) Parent #1 - pathogenic g.182468562A>C - c.481+2T>G - CERKL_000026 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+/. 2i c.481+2T>G r.spl p.? Parent #2 ACMG pathogenic g.182468562A>C g.181603835A>C - - CERKL_000026 - PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - - Germline - - - - - DNA SEQ, SEQ-NG - smMIP-based 105 iMD/AMD genes macular dystrophy 066777 PubMed: Hitti-Malin 2024, Journal: Hitti-Malin 2024 - M - - - - - - - 1 Rebekkah Hitti-Malin
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