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Macular Dystrophy/Stargardt Disease v0.40 CLEC3B Zornitza Stark Marked gene: CLEC3B as ready
Macular Dystrophy/Stargardt Disease v0.40 CLEC3B Zornitza Stark Gene: clec3b has been classified as Green List (High Evidence).
Macular Dystrophy/Stargardt Disease v0.40 CLEC3B Zornitza Stark Tag founder tag was added to gene: CLEC3B.
Macular Dystrophy/Stargardt Disease v0.40 CLEC3B Chirag Patel Classified gene: CLEC3B as Green List (high evidence)
Macular Dystrophy/Stargardt Disease v0.40 CLEC3B Chirag Patel Gene: clec3b has been classified as Green List (High Evidence).
Macular Dystrophy/Stargardt Disease v0.39 CLEC3B Chirag Patel gene: CLEC3B was added
gene: CLEC3B was added to Macular Dystrophy/Stargardt Disease. Sources: Literature
Mode of inheritance for gene: CLEC3B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CLEC3B were set to PMID: 35331648
Phenotypes for gene: CLEC3B were set to Macular dystrophy, retinal, 4, OMIM #619977
Review for gene: CLEC3B was set to GREEN
Added comment: 12 affected individuals from 5 multigenerational Japanese families in a small village in Miyazaki diagnosed with autosomal dominant maculoretinopathy. WES identified a pathogenic variant (p.Ala180Asp) in CLEC3B, which encodes tetranectin, a plasminogen kringle-4 binding protein. Variant cosegregated with the ocular phenotype.

Mice that received subretinal injections with CLEC3B variant displayed multiple subretinal hyperreflective deposits, reduced retinal thickness, and decreased electroretinographic responses. The optokinetic tracking response indicated that spatial frequency was significantly lower (P < .05), implying impaired visual function in the mice.
Sources: Literature