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.

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/. 2 c.390G>A r.(?) p.(Trp130*) - Both (homozygous) - pathogenic (recessive) g.112687025G>A g.111929448G>A - - MERTK_000002 - PubMed: Wang 2014a - - Germline - - - - - DNA SEQ-NG-I - - RP - PubMed: Wang 2014a - - - (United States) - - - - - 1 Feng Wang
+/. 2 c.390G>A r.(?) p.(Trp130*) Ig-like C2 type I Parent #1 - pathogenic g.112687025G>A g.111929448G>A - - MERTK_000002 - PubMed: Ge 2015 - - Germline - - - - - DNA SEQ - - retinal disease 5VR+W.92 PubMed: Ge 2015 simplex case - - United States America-N - - - - 1 Isabelle Audo
+?/. 2 c.390G>A r.(?) p.(Trp130*) - Both (homozygous) - likely pathogenic g.112687025G>A g.111929448G>A c.390G>A, p.(Trp130*) - MERTK_000002 Homozygous PubMed: Tayebi 2019 - - Germline yes - - - - DNA SEQ-NG-I blood 108-gene panel targeted resequencing using MIPs library prep retinal disease 066882 PubMed: Tayebi 2019 - - - Iran - - - - - 1 LOVD
?/. - c.390G>A r.(?) p.(Trp130*) - Unknown - VUS g.112687025G>A g.111929448G>A MERTK nucleotide 1, protein 1:c.390G>A, p.Trp130* nucleotide 2, protein 2:c.1605-2A>G, p.? - MERTK_000002 heterozygous, ACMG unclassified - no access to supplementary table 2 PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 75 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
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