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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+?/. - c.436_437del r.(?) p.(Gln146Valfs*5) - Parent #2 - likely pathogenic g.112687071_112687072del g.111929494_111929495del 433_434delAC - MERTK_000155 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 819 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.436_437del r.(?) p.(Gln146Valfs*5) - Unknown - likely pathogenic g.112687071_112687072del g.111929494_111929495del c.436_437delCA - MERTK_000155 - PubMed: Hariri 2018 - - Germline ? - - - - DNA SEQ - retrospective analysis retinal disease - PubMed: Hariri 2018 - ? - - - - - - - 1 LOVD
+?/. 7 c.436_437del r.(?) p.(Gln146Valfs*5) - Both (homozygous) - likely pathogenic g.112687071_112687072del - c.436_437del - MERTK_000155 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
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