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| Polydactyly v0.240 | TMEM107 | Bryony Thompson Classified gene: TMEM107 as Green List (high evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Polydactyly v0.240 | TMEM107 | Bryony Thompson Gene: tmem107 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Polydactyly v0.239 | TMEM107 |
Bryony Thompson gene: TMEM107 was added gene: TMEM107 was added to Polydactyly. Sources: Expert list Mode of inheritance for gene: TMEM107 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TMEM107 were set to 22698544; 26123494; 26518474 Phenotypes for gene: TMEM107 were set to Meckel syndrome 13 MIM#617562; Orofaciodigital syndrome XVI MIM#617563 Review for gene: TMEM107 was set to GREEN gene: TMEM107 was marked as current diagnostic Added comment: At least four unrelated families with polydactyly as a feature of the condition and a supporting null mouse model. Sources: Expert list |
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