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| Regression v1.0 | TNK2 | Gene migrated from ENSG00000061938 to ENSG00000061938 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Regression v0.608 | Sarah Milton Copied gene TNK2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Regression v0.608 | TNK2 |
Sarah Milton gene: TNK2 was added gene: TNK2 was added to Regression. Sources: Expert Review Amber,Victorian Clinical Genetics Services Mode of inheritance for gene: TNK2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: TNK2 were set to 27977884; 23686771; 31517310 Phenotypes for gene: TNK2 were set to late onset infantile epilepsy; Mayer-Rokitansky-Küster-Hauser syndrome |
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