Full data view for gene MERTK

This database is one of the "Eye disease" gene variant databases.
Information The variants shown are described using the NM_006343.2 transcript reference sequence.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. 9 c.1450G>A r.spl? p.(Gly484Ser) transmembrane and kinase domain Parent #1 - pathogenic g.112751981G>A g.111994404G>A - - MERTK_000070 Align GVGD class C0; SIFT tolerated (score 0.29); Mutation Taster disease causing (p value=1) Polyphen2 benign with a score of 0.444 (sensitivity: 0.89; specificity: 0.90) and conserved residue Predicted to affect splicing PubMed: Audo 2018 - rs527236084 Germline yes - - - - DNA SEQ - - retinal disease ? PubMed: Audo 2018 - - - Italy - - - - - 1 Isabelle Audo
+/. 9 c.1450G>A r.(?) p.(Gly484Ser) transmembrane and kinase domain Both (homozygous) - pathogenic g.112751981G>A g.111994404G>A - - MERTK_000070 Align GVGD class C0; SIFT tolerated (score 0.29); Mutation Taster disease causing (p value=1) Polyphen2 benign with a score of 0.444 (sensitivity: 0.89; specificity: 0.90) and conserved residue Predicted to affect splicing PubMed: Eisenberger 2013 - rs527236084 Germline - - - - - DNA SEQ - - retinal disease ? PubMed: Eisenberger 2013 - - - Italy - - - - - 1 Isabelle Audo
+/. - c.1450G>A r.spl p.(Gly484Ser) - Parent #2 - pathogenic g.112751981G>A g.111994404G>A - - MERTK_000070 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K6488 PubMed: Oishi 2014 simplex case - - Japan - - - - - 1 LOVD
+/. 15 c.1450G>A r.(?) p.(Gly484Ser) - Both (homozygous) - pathogenic g.112751981G>A - c.1450G>A - MERTK_000070 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M no Italy - - - - - 1 LOVD
+?/. - c.1450G>A r.(?) p.(Gly484Ser) - Both (homozygous) ACMG likely pathogenic g.112751981G>A g.111994404G>A MERTK c.1450G>A, p.(Gly484Ser), c.1450G>A, p.(Gly484Ser) - MERTK_000070 homozygous PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 156 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.1450G>A r.(?) p.(Gly484Ser) - Unknown ACMG likely pathogenic g.112751981G>A g.111994404G>A MERTK:NM_006343 c.G1450A, p.G484S - MERTK_000070 heterozygous, individual solved, variant causal PubMed: Rodriguez-Munoz 2020 - - Germline yes - - - - DNA SEQ-NG-I blood - retinal disease RPN-442 PubMed: Rodriguez-Munoz 2020 family fRPN-197, proband F - Spain - - - - - 1 LOVD
+?/. 15 c.1450G>A r.(?) p.(Gly484Ser) - Both (homozygous) - likely pathogenic g.112751981G>A - c.1450G>A - MERTK_000070 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing LCA - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+?/. 15 c.1450G>A r.(?) p.(Gly484Ser) - Both (homozygous) - likely pathogenic g.112751981G>A - c.1450G>A - MERTK_000070 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
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