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| Mendeliome v1.4359 | GPRASP2 | Bryony Thompson Marked gene: GPRASP2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4359 | GPRASP2 | Bryony Thompson Gene: gprasp2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4359 | GPRASP2 |
Bryony Thompson gene: GPRASP2 was added gene: GPRASP2 was added to Mendeliome. Sources: Literature Mode of inheritance for gene: GPRASP2 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: GPRASP2 were set to 28096187; 41688572 Phenotypes for gene: GPRASP2 were set to X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome MONDO:0044702 Review for gene: GPRASP2 was set to RED Added comment: A single family reported segregating a hemizygous delins with deafness and a supporting deficient mouse model. Sources: Literature |
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