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.

13 entries on 1 page. Showing entries 1 - 13.
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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     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. 2 c.345C>G r.(?) p.(Cys115Trp) Ig-like C2 type I Parent #2 - VUS g.112686980C>G g.111929403C>G - - MERTK_000051 - PubMed: Wang 2014b - rs772421550 Germline - - - - - DNA SEQ - - retinal disease 21 PubMed: Wang 2014b - F - United States - - - - - 1 Johan den Dunnen
+/. 2 c.345C>G r.(?) p.(Cys115Trp) Ig-like C2 type I Parent #2 - pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 Align GVGD class C65; SIFT deleterious (score 0); Mutation Taster disease causing (p value=1); Polyphen2 probably damaging with a score of 1 (sensitivity: 0.00; specificity: 1.00) and conserved residue Khan 2018 - rs772421550 Germline - - - - - DNA SEQ - - ? ? Khan 2017 - - - United Kingdom (Great Britain) - - - - - 2 Isabelle Audo
+/. 2 c.345C>G r.(?) p.(Cys115Trp) Ig-like C2 type I Parent #2 - pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 Align GVGD class C65; SIFT deleterious (score 0); Mutation Taster disease causing (p value=1); Polyphen2 probably damaging with a score of 1 (sensitivity: 0.00; specificity: 1.00) and conserved residue PubMed: Eisenberger 2013 - rs772421550 Germline - - - - - DNA SEQ - - retinal disease ? PubMed: Eisenberger 2013 - - - Germany - - - - - 1 Isabelle Audo
+/. 2 c.345C>G r.(?) p.(Cys115Trp) Ig-like C2 type I Parent #2 - pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 putative compound hetetorzygous;A lign GVGD class C65; SIFT deleterious (score 0); Mutation Taster disease causing (p value=1); Polyphen2 probably damaging with a score of 1 (sensitivity: 0.00; specificity: 1.00) and conserved residue PubMed: Audo 2018 - rs772421550 Germline - - - - - DNA SEQ - - retinal disease ? PubMed: Audo 2018 - - - France - - - - - 1 Isabelle Audo
+?/. - c.345C>G r.(?) p.(Cys115Trp) - Unknown - likely pathogenic g.112686980C>G g.111929403C>G MERTK(NM_006343.3):c.345C>G (p.C115W) - MERTK_000051 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.345C>G r.(?) p.(Cys115Trp) - Parent #1 - pathogenic (recessive) g.112686980C>G g.111929403C>G - - MERTK_000051 - PubMed: Avela 2018 - - Germline - - - - - DNA SEQ-NG - - retinal disease Pat31 PubMed: Avela 2018 - - - Finland - - - - - 1 LOVD
+?/. - c.345C>G r.(?) p.(Cys115Trp) - Both (homozygous) - likely pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 44 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.345C>G r.(?) p.(Cys115Trp) - Parent #1 - pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 - PubMed: Khan 2017 - - Germline - - - - - DNA SEQ-NG - 105-gene panel retinal disease 3259 PubMed: Khan 2017 see paper - - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. 2 c.345C>G r.(?) p.(Cys115Trp) - Unknown ACMG likely pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 - Tracewska 2021, MolVis in press - - Germline - 0 (in-house database, ~5000 samples) - - - DNA SEQ-NG-I, SEQ blood targeted resequencing using MIPs library prep, 108-gene panel retinal disease 261 Tracewska 2021, MolVis in press proband M no Poland Slavic - - yes - 1 LOVD
+?/. 2 c.345C>G r.(?) p.(Cys115Trp) - Maternal (confirmed) ACMG likely pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 - Tracewska 2021, MolVis in press - - Germline yes 0 (in-house database, ~5000 samples) - - - DNA SEQ-NG-I, SEQ blood targeted resequencing using MIPs library prep, 108-gene panel retinal disease 307 Tracewska 2021, MolVis in press proband M no Poland Slavic - - yes - 2 LOVD
+?/. 2 c.345C>G r.(?) p.(Cys115Trp) - Maternal (confirmed) ACMG likely pathogenic g.112686980C>G g.111929403C>G - - MERTK_000051 - Tracewska 2021, MolVis in press - - Germline yes 0 (in-house database, ~5000 samples) - - - DNA SEQ buccal cells targeted resequencing using MIPs library prep, 108-gene panel retinal disease 549 Tracewska 2021, MolVis in press brother M no Poland Slavic - - yes - 1 LOVD
+/. 6 c.345C>G r.(?) p.(Ser115Arg) - Unknown - pathogenic g.112686980C>G - c.345C>G - MERTK_000051 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M no Germany - - - - - 1 LOVD
+?/. - c.345C>G r.(?) p.(Cys115Trp) - Both (homozygous) ACMG likely pathogenic g.112686980C>G g.111929403C>G MERTK c.345C>G, p.(Cys115Trp), c.345C>G, p.(Cys115Trp) - MERTK_000051 homozygous PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 151 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
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