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     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 17 c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] r.(?) p.[(Ile582Glyfs*4);(Arg584Met)] - Parent #1 - likely pathogenic g.112760722_112760729delinsT - c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] - MERTK_000076 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+?/. 17 c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] r.(?) p.[(Ile582Glyfs*4);(Arg584Met)] - Parent #2 - likely pathogenic g.112760722_112760729delinsT - c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] - MERTK_000076 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. 17 c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] r.(?) p.[(Ile582Glyfs*4);(Arg584Met)] - Parent #2 - likely pathogenic g.112760722_112760729delinsT - c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] - MERTK_000076 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. 17 c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] r.(?) p.[(Ile582Glyfs*4);(Arg584Met)] - Both (homozygous) - likely pathogenic g.112760722_112760729delinsT - c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] - MERTK_000076 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing retinal disease - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. 17 c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] r.(?) p.[(Ile582Glyfs*4);(Arg584Met)] - Both (homozygous) - likely pathogenic g.112760722_112760729delinsT - c.[1744_1750del;1751G>T]; p.[(Ile582Glyfs*4);(Arg584Met)] - MERTK_000076 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
+/. 12 c.1744_1751delinsT r.(?) p.(Ile582*) kinase domain Both (homozygous) - pathogenic g.112760722_112760729delinsT g.112003145_112003152delinsT - - MERTK_000076 - PubMed: Eisenberger 2013 - - Germline - - - - - DNA SEQ - - LCA ? PubMed: Eisenberger 2013 - - - Turkey - - - - - 1 Isabelle Audo
+/. 17 c.1744_1751delinsT r.(?) p.(Arg582Leufs*10) - Unknown - pathogenic g.112760722_112760729delinsT - c.1744_1751delinsT - MERTK_000076 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M yes Turkey - - - - - 1 LOVD
+/. - c.1744_1751delinsT r.(?) p.(Ile582Ter) - Both (homozygous) ACMG pathogenic (recessive) g.112760722_112760729delinsT g.112003145_112003152delinsT - - MERTK_000076 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? ARRP-477 PubMed: Weisschuh 2024 family, 3 affected M - Germany - - - - - 3 Johan den Dunnen
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