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| Mendeliome v1.4376 | MARK3 | Bryony Thompson Marked gene: MARK3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4376 | MARK3 | Bryony Thompson Gene: mark3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4376 | MARK3 |
Bryony Thompson gene: MARK3 was added gene: MARK3 was added to Mendeliome. Sources: Literature Mode of inheritance for gene: MARK3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MARK3 were set to 29771303 Phenotypes for gene: MARK3 were set to visual impairment and progressive phthisis bulbi MONDO:0032655 Review for gene: MARK3 was set to RED Added comment: A single consanguineous family with a homozygous variant and a supporting drosphila model. Sources: Literature |
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