| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Congenital hypothyroidism v1.3 | DTX2 | Rylee Peters Marked gene: DTX2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v1.3 | DTX2 | Rylee Peters Gene: dtx2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v1.3 | DTX2 |
Rylee Peters gene: DTX2 was added gene: DTX2 was added to Congenital hypothyroidism. Sources: Literature Mode of inheritance for gene: DTX2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DTX2 were set to 42192612 Phenotypes for gene: DTX2 were set to Congenital hypothyroidism, MONDO:0018612, DTX2-related Review for gene: DTX2 was set to RED Added comment: PMID: 42192612 reports 1 individual from 1 family with biallelic missense DTX2 variants (variants not phased/segregated) presenting with congenital hypothyroidism, isolated thyroid dysfunction, childhood‑onset. Zebrafish morpholino knockdown of dtx2 caused thyroid hypoplasia and reduced T4. Sources: Literature |
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| Congenital hypothyroidism v0.125 | Rylee Peters Added reviews for gene DTX2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.124 | Rylee Peters Added reviews for gene DTX2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.123 | Rylee Peters Added reviews for gene DTX2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.122 | Rylee Peters Copied gene DTX2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.122 | DTX2 |
Rylee Peters gene: DTX2 was added gene: DTX2 was added to Congenital hypothyroidism. Sources: Expert Review Red,Literature Mode of inheritance for gene: DTX2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DTX2 were set to 42192612 Phenotypes for gene: DTX2 were set to Congenital hypothyroidism, MONDO:0018612, DTX2-related |
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