| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Deafness_IsolatedAndComplex v1.333 | Zornitza Stark Copied gene XPOT from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.333 | XPOT |
Zornitza Stark gene: XPOT was added gene: XPOT was added to Deafness_IsolatedAndComplex. Sources: Expert Review Green,Literature preprint tags were added to gene: XPOT. Mode of inheritance for gene: XPOT was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: XPOT were set to 10.64898/2026.01.28.26344748 Phenotypes for gene: XPOT were set to Syndromic disease, MONDO:0002254 |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||