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| Hand and foot malformations v1.7 | S1PR2 | chirag patel Marked gene: S1PR2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v1.7 | S1PR2 | chirag patel Gene: s1pr2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v1.7 | chirag patel Copied gene S1PR2 from panel Deafness_IsolatedAndComplex | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hand and foot malformations v1.7 | S1PR2 |
chirag patel gene: S1PR2 was added gene: S1PR2 was added to Hand and foot malformations. Sources: Expert Review Green,Expert list Mode of inheritance for gene: S1PR2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: S1PR2 were set to 26805784; 29776397; 27383011 Phenotypes for gene: S1PR2 were set to Sensorineural hearing loss disorder MONDO:0020678, S1PR2-related; Congenital limb malformation, MONDO:0019054, S1PR2-related |
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