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Primary Ovarian Insufficiency_Premature Ovarian Failure v0.321 MCM9 Zornitza Stark Phenotypes for gene: MCM9 were changed from Ovarian dysgenesis 4, MIM#616185 to Ovarian dysgenesis 4, MIM#616185; Hereditary neoplastic syndrome MONDO:0015356
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.320 MCM9 Zornitza Stark Publications for gene: MCM9 were set to 25480036; 26771056; 33538981; 33095795
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.319 MCM9 Zornitza Stark edited their review of gene: MCM9: Changed publications: 25480036, 26771056, 33538981, 33095795, 26806154, 34556653, 32841224, 32613604, 37378315; Changed phenotypes: Ovarian dysgenesis 4, MIM# 616185, Hereditary neoplastic syndrome MONDO:0015356
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.319 MCM9 Zornitza Stark commented on gene: MCM9: Please note emerging link with Lynch-like syndrome: PMIDs 26806154; 34556653; 32841224; 32613604; 37378315
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.300 MCM9 Zornitza Stark Marked gene: MCM9 as ready
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.300 MCM9 Zornitza Stark Gene: mcm9 has been classified as Green List (High Evidence).
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.300 MCM9 Zornitza Stark Phenotypes for gene: MCM9 were changed from Ovarian dysgenesis 4, 616185 to Ovarian dysgenesis 4, MIM#616185
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.299 MCM9 Zornitza Stark Publications for gene: MCM9 were set to
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.298 MCM9 Zornitza Stark reviewed gene: MCM9: Rating: GREEN; Mode of pathogenicity: None; Publications: 25480036, 26771056, 33538981, 33095795; Phenotypes: Ovarian dysgenesis 4, MIM# 616185; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Primary Ovarian Insufficiency_Premature Ovarian Failure v0.0 MCM9 Bryony Thompson gene: MCM9 was added
gene: MCM9 was added to Amenorrhoea. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: MCM9 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: MCM9 were set to Ovarian dysgenesis 4, 616185