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| Deafness_IsolatedAndComplex v2.0 | MAP2K1 | Gene migrated from ENSG00000169032 to ENSG00000169032 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.195 | MAP2K1 | chirag patel Classified gene: MAP2K1 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.195 | MAP2K1 | chirag patel Gene: map2k1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.193 | MAP2K1 |
chirag patel gene: MAP2K1 was added gene: MAP2K1 was added to Deafness_IsolatedAndComplex. Sources: Literature Mode of inheritance for gene: MAP2K1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MAP2K1 were set to PMID: 20301557 Phenotypes for gene: MAP2K1 were set to Noonan Syndrome with Multiple Lentigines, OMIM # 615279 Review for gene: MAP2K1 was set to GREEN gene: MAP2K1 was marked as current diagnostic Added comment: Established gene-disease association. Sensorineural hearing loss is present in ~20% of 'Noonan Syndrome with Multiple Lentigines' Sources: Literature |
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