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| Clefting disorders v1.0 | KMT2D | Gene migrated from ENSG00000167548 to ENSG00000167548 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Clefting disorders v0.279 | chirag patel Added reviews for gene KMT2D from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Clefting disorders v0.0 | KMT2D |
Zornitza Stark gene: KMT2D was added gene: KMT2D was added to Clefting_GEL. Sources: Expert Review,Emory Genetics Laboratory,UKGTN,Radboud University Medical Center, Nijmegen,Expert Review Green,Literature Mode of inheritance for gene: KMT2D was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KMT2D were set to 22126750; 20711175; 21671394; 26049589; 25142838 Phenotypes for gene: KMT2D were set to Kabuki syndrome 1, 147920 |
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