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| Deafness_IsolatedAndComplex v2.10 | S1PR2 | chirag patel Phenotypes for gene: S1PR2 were changed from Deafness, autosomal recessive 68, MIM# 610419 to Sensorineural hearing loss disorder MONDO:0020678, S1PR2-related; Congenital limb malformation, MONDO:0019054, S1PR2-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v2.9 | S1PR2 | chirag patel reviewed gene: S1PR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 26805784, 29776397; Phenotypes: Sensorineural hearing loss disorder MONDO:0020678, S1PR2-related, Congenital limb malformation, MONDO:0019054, S1PR2-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v2.0 | S1PR2 | Gene migrated from ENSG00000267534 to ENSG00000267534 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.155 | S1PR2 | Zornitza Stark Marked gene: S1PR2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.155 | S1PR2 | Zornitza Stark Gene: s1pr2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.155 | S1PR2 | Zornitza Stark Classified gene: S1PR2 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.155 | S1PR2 | Zornitza Stark Gene: s1pr2 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v0.154 | S1PR2 |
Zornitza Stark gene: S1PR2 was added gene: S1PR2 was added to Deafness_MelbourneGenomics_VCGS. Sources: 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 Deafness, autosomal recessive 68, MIM# 610419 Review for gene: S1PR2 was set to GREEN Added comment: Three unrelated families and a mouse model. Sources: Expert list |
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