Activity
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3 actions
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| Microcephaly v0.636 | NUP37 | Zornitza Stark Marked gene: NUP37 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Microcephaly v0.636 | NUP37 | Zornitza Stark Gene: nup37 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Microcephaly v0.636 | NUP37 |
Zornitza Stark gene: NUP37 was added gene: NUP37 was added to Microcephaly. Sources: Expert list 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 Microcephaly 24, primary, autosomal recessive, MIM# 618179 Review for gene: NUP37 was set to RED Added comment: Single family reported with nephrotic syndrome and microcephaly. Sources: Expert list |
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