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| Hereditary Pigmentary Disorders v2.0 | STK11 | Gene migrated from ENSG00000118046 to ENSG00000118046 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Pigmentary Disorders v1.7 | STK11 | Zornitza Stark Marked gene: STK11 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Pigmentary Disorders v1.7 | STK11 | Zornitza Stark Gene: stk11 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Pigmentary Disorders v1.7 | STK11 | Sangavi Sivagnanasundram Classified gene: STK11 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Pigmentary Disorders v1.7 | STK11 | Sangavi Sivagnanasundram Gene: stk11 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Pigmentary Disorders v1.6 | STK11 |
Sangavi Sivagnanasundram gene: STK11 was added gene: STK11 was added to Hereditary Pigmentary Disorders. Sources: Expert Review Mode of inheritance for gene: STK11 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: STK11 were set to 15121768; 739570 Phenotypes for gene: STK11 were set to Peutz-Jeghers syndrome MONDO:0008280 Review for gene: STK11 was set to GREEN Added comment: PJS is characterised by the development of gastrointestinal PJS-type hamartomatous polyps and mucocutaneous hyperpigmentation, which most often presents in childhood and fades by puberty. Classified as DEFINITIVE by ClinGen Hereditary Cancer GCEP on 20/12/2023 - https://search.clinicalgenome.org/CCID:006288 Sources: Expert Review |
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