| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Mendeliome v0.6995 | NUP37 | Zornitza Stark Phenotypes for gene: NUP37 were changed from Nephrotic syndrome to Nephrotic syndrome; Microcephaly 24, primary, autosomal recessive, MIM# 618179 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.6994 | NUP37 |
Zornitza Stark changed review comment from: Single family reported with nephrotic syndrome. Sources: Literature; to: Single family reported with nephrotic syndrome and microcephaly. Sources: Literature |
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| Mendeliome v0.6994 | NUP37 | Zornitza Stark edited their review of gene: NUP37: Changed phenotypes: Nephrotic syndrome, Microcephaly 24, primary, autosomal recessive, MIM# 618179 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.1007 | NUP37 | Zornitza Stark Marked gene: NUP37 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.1007 | NUP37 | Zornitza Stark Gene: nup37 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v0.388 | NUP37 |
Zornitza Stark gene: NUP37 was added gene: NUP37 was added to Mendeliome_VCGS. Sources: Literature Mode of inheritance for gene: NUP37 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NUP37 were set to 30179222 Phenotypes for gene: NUP37 were set to Nephrotic syndrome Review for gene: NUP37 was set to RED Added comment: Single family reported with nephrotic syndrome. Sources: Literature |
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