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| Primary Ovarian Insufficiency_Premature Ovarian Failure v1.0 | SOX8 | Gene migrated from ENSG00000005513 to ENSG00000005513 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.421 | SOX8 | Zornitza Stark Marked gene: SOX8 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.421 | SOX8 | Zornitza Stark Gene: sox8 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.421 | SOX8 | Zornitza Stark Phenotypes for gene: SOX8 were changed from Neurodevelopmental disorder (MONDO:0700092), SOX8-related; Infertility disorder, MONDO:0005047, SOX8-related to Infertility disorder, MONDO:0005047, SOX8-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.420 | SOX8 | Zornitza Stark Mode of inheritance for gene: SOX8 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.419 | Zornitza Stark Copied gene SOX8 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Primary Ovarian Insufficiency_Premature Ovarian Failure v0.419 | SOX8 |
Zornitza Stark gene: SOX8 was added gene: SOX8 was added to Primary Ovarian Insufficiency_Premature Ovarian Failure. Sources: Expert Review Red,Literature Mode of inheritance for gene: SOX8 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: SOX8 were set to 39595984; 38235364; 36631813; 35734438; 29373757 Phenotypes for gene: SOX8 were set to Neurodevelopmental disorder (MONDO:0700092), SOX8-related; Infertility disorder, MONDO:0005047, SOX8-related |
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