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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. 9 c.1441C>T r.spl p.(Pro481Ser) 2nd FN-III domain Unknown - benign g.112751972C>T g.111994395C>T - - MERTK_000069 predicted to affect splicing; Align GVGD class C35; SIFT deleterious (score 0); Mutation Taster disease causing (p value=1) probably damaging with a score of 1 (sensitivity: 0; specificity: 1) and conserved residue PubMed: Xu 2014 - rs781442827 Germline - - - - - DNA SEQ - - retinal disease RP207 PubMed: Xu 2014 - - - China - - - - - 2 Isabelle Audo
?/. - c.1441C>T r.(?) p.(Pro481Ser) - Unknown - VUS g.112751972C>T g.111994395C>T - - MERTK_000069 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs781442827 Germline - 1/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 1 Yoshito Koyanagi
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