Activity
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3 actions
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| Hereditary Neuropathy_CMT - isolated v1.2 | IQGAP3 | Zornitza Stark Marked gene: IQGAP3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy_CMT - isolated v1.2 | IQGAP3 | Zornitza Stark Gene: iqgap3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy_CMT - isolated v1.2 | IQGAP3 |
Zornitza Stark gene: IQGAP3 was added gene: IQGAP3 was added to Hereditary Neuropathy_CMT - isolated. Sources: Literature Mode of inheritance for gene: IQGAP3 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: IQGAP3 were set to 32341455 Phenotypes for gene: IQGAP3 were set to Hereditary neuropathy Review for gene: IQGAP3 was set to RED Added comment: Single multiplex family reported with intronic variant and limited functional data. Sources: Literature |
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