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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+/. 16 c.2164C>T r.(?) p.(Arg722*) - Both (homozygous) - pathogenic g.112777074C>T g.112019497C>T - - MERTK_000035 - Sharon, submitted - - Germline - - - - - DNA SEQ - - retinal disease - Sharon, submitted - M yes Israel Arab-Muslim - - - - 2 Dror Sharon
+/. 16 c.2164C>T r.(?) p.(Arg722*) kinase domain Paternal (confirmed) - pathogenic g.112777074C>T g.112019497C>T - - MERTK_000035 - PubMed: McHenry 2004 - rs541717028 Germline - - - - - DNA SEQ - - CORD ? PubMed: McHenry 2004 - - - United States - - - - - 1 Isabelle Audo
+/. 16 c.2164C>T r.(?) p.(Arg722*) kinase domain Parent #1 - pathogenic g.112777074C>T g.112019497C>T - - MERTK_000035 - PubMed: Wang 2014b - rs541717028 Germline - - - - - DNA SEQ - - CORD 31 PubMed: Wang 2014b - F - United States - - - - - 1 Isabelle Audo
+/. - c.2164C>T r.(?) p.(Arg722*) - Unknown ACMG pathogenic g.112777074C>T - - - MERTK_000035 - PubMed: Sharon 2019 - - Germline - 5/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - 5 Global Variome, with Curator vacancy
+/. - c.2164C>T r.(?) p.(Arg722*) - Unknown - pathogenic (recessive) g.112777074C>T - 2:112777074C>T ENST00000295408.4:c.2164C>T (Arg722Ter) - MERTK_000035 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001054 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+/. - c.2164C>T r.(?) p.(Arg722*) - Unknown - pathogenic g.112777074C>T g.112019497C>T MERTK c.2164C>T, p.Arg722Ter - MERTK_000035 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001054 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
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