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.

20 entries on 1 page. Showing entries 1 - 20.
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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     
+?/. 16i c.2189+1G>T r.spl p.? - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T - - MERTK_000005 - PubMed: de Castro-Miró 2014 - - Germline yes - - - - DNA SEQ-NG-I Whole blood - retinal disease - PubMed: de Castro-Miró 2014 - F ? Spain - - - - - 1 Marta de Castro-Miró
+/. 16i c.2189+1G>T r.spl p.? kinase domain Both (homozygous) - pathogenic g.112777100G>T g.112019523G>T - - MERTK_000005 - PubMed: Patel 2016 - rs371956016 Germline - - - - - DNA SEQ - - CORD 13DG0011 PubMed: Patel 2016 - - - Saudi Arabia - - - - - 1 Johan den Dunnen
+/. 16i c.2189+1G>T r.(ex16del) p.(His694Valfs*4) kinase domain Both (homozygous) - pathogenic g.112777100G>T g.112019523G>T - - MERTK_000005 - PubMed: Ebermann 2007 - rs371956016 Germline - - - - - DNA SEQ - - CORD ? PubMed: Ebermann 2007 - - - Morocco - - - - - 1 Isabelle Audo
+?/. - c.2189+1G>T r.spl p.? - Both (homozygous) - likely pathogenic (recessive) g.112777100G>T g.112019523G>T - - MERTK_000005 - PubMed: Holtan 2020 - - Germline - 6/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 6 homozygous patients - - Norway - - - - - 6 Global Variome, with Curator vacancy
+?/. 16i c.2189+1G>T r.(?) p.(?) - Unknown - likely pathogenic g.112777100G>T g.112019523G>T MERTK IVS16 c.2189+1G>T p.(?) - MERTK_000005 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I, arrayCGH - - retinal disease RP-0236 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 16i c.2189+1G>T r.(?) p.(?) - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T MERTK IVS16 c.2189+1G>T p.(?), IVS16 c.2189+1G>T p.(?) - MERTK_000005 homozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA arraySNP - - retinal disease RP-1236 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 16i c.2189+1G>T r.(?) p.(?) - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T MERTK IVS16 c.2189+1G>T p.(?), IVS16 c.2189+1G>T p.(?) - MERTK_000005 homozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA arraySNP - - retinal disease RP-2086 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - likely pathogenic g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: de Castro-Miró-2014 - - Germline - - - - - DNA arraySNP - RD-xip retinal disease 17NCE PubMed: de Castro-Miró-2014 - - - - - - - - - 1 LOVD
+?/. - c.2189+1G>T r.(?) p.(?) - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T MERTK c.2189+1G>T, p.(?) - MERTK_000005 homozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 87 PubMed: Jauregui 2020 - F - (United States) Hispanic - - - - 1 LOVD
+?/. 16 c.2189+1G>T r.spl p.(?) - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T MERTK c.2189+1G>T, splice site - MERTK_000005 homozygous PubMed: Gliem 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood whole exome sequencing retinal disease 137 PubMed: Gliem 2020 - M - (Germany) - - - - - 1 LOVD
+?/. 16 c.2189+1G>T r.spl p.(?) - Both (homozygous) - likely pathogenic g.112777100G>T g.112019523G>T MERTK c.2189+1G>T, splice site - MERTK_000005 homozygous PubMed: Gliem 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood whole exome sequencing retinal disease 138 PubMed: Gliem 2020 - F - (Germany) - - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - IVS16+1G>T - MERTK_000005 - PubMed: Brea-Fernández 2008 - - Germline yes - - - - DNA, RNA SNPlex, SEQ, RT-PCR - - retinal disease II.2, II.3, II.14 PubMed: Brea-Fernández 2008 - F;M yes Spain - - - - - 3 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Unknown - pathogenic (recessive) g.112777100G>T - IVS16+1G>T - MERTK_000005 - PubMed: Brea-Fernández 2008 - - Germline yes - - - - DNA, RNA SNPlex, SEQ, RT-PCR - - Healthy/Control II.5, II.9, II.12, II.15 PubMed: Brea-Fernández 2008 Healthy carriers F;M yes Spain - - - - - 4 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Unknown - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease I-1 PubMed: Charbel Issa 2009 Carrier mother of II - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Unknown - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease I-2 PubMed: Charbel Issa 2009 Carrier father of II - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease II-1 PubMed: Charbel Issa 2009 - - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease II-3 PubMed: Charbel Issa 2009 - - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease II-4 PubMed: Charbel Issa 2009 visual acuity for the last 3 years - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease II-5 PubMed: Charbel Issa 2009 - - yes - Moroccan - - - - 1 LOVD
+/. 19 c.2189+1G>T r.spl? p.? - Both (homozygous) - pathogenic (recessive) g.112777100G>T - c.2189+1G>T - MERTK_000005 - PubMed: Charbel Issa 2009 - - Germline - - - - - DNA ? - - retinal disease II-6 PubMed: Charbel Issa 2009 reported deteriorating visual acuity in recent years as well as poor orientation in the dark - yes - Moroccan - - - - 1 LOVD
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