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.225del r.(?) p.(Gly76Glufs*3) N-terminus fragment Parent #1 - pathogenic g.112686860del g.111929283del - - MERTK_000047 - PubMed: Oishi 2014 - rs527236083 Germline - - - - - DNA SEQ - - retinal disease K6484 PubMed: Oishi 2014 - - - Japan - - - - - 1 Isabelle Audo
+/. - c.225del r.(?) p.(Gly76GlufsTer3) - Both (homozygous) - pathogenic g.112686860del g.111929283del 225delA - MERTK_000047 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K6151 PubMed: Oishi 2014 family - - Japan - - - - - 1 LOVD
+/. - c.225del r.(?) p.(Gly76GlufsTer3) - Parent #1 - pathogenic g.112686860del g.111929283del 225delA - MERTK_000047 - PubMed: Oishi 2014 - - Germline - - - - - DNA SEQ-NG - 193-gene panel retinal disease K6488 PubMed: Oishi 2014 simplex case - - Japan - - - - - 1 LOVD
+?/. 4 c.225del r.(?) p.(Pro76Glnfs*3) - Unknown - likely pathogenic (recessive) g.112686860del - c.225delA - MERTK_000047 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
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