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Congenital hypothyroidism v2.8 POLR2C Ivone Leong Phenotypes for gene: POLR2C were changed from Primary ovarian insufficiency to hypothyroidism, MONDO:0005420
Congenital hypothyroidism v2.7 POLR2C Ivone Leong Classified gene: POLR2C as Red List (low evidence)
Congenital hypothyroidism v2.7 POLR2C Ivone Leong Gene: polr2c has been classified as Red List (Low Evidence).
Congenital hypothyroidism v2.6 POLR2C Ivone Leong Tag watchlist was removed from gene: POLR2C.
Congenital hypothyroidism v2.6 POLR2C Ivone Leong changed review comment from: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with a phenotype in OMIM or Gene2Phenotype. The affected patients in PMID: 29367954 also had hypothyroidism (3/5), thrombocytopenia (2/5) and pernicious anaemia (2/5).; to: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with a phenotype in OMIM or Gene2Phenotype. The affected patients in PMID: 29367954 also had hypothyroidism (3/5), thrombocytopenia (2/5) and pernicious anaemia (2/5). The entries in ClinVar did not mention any other phenotype. So therefore this gene has been given a Red rating.
Congenital hypothyroidism v2.6 POLR2C Ivone Leong Entity copied from Primary ovarian insufficiency v1.62
Congenital hypothyroidism v2.6 POLR2C Ivone Leong gene: POLR2C was added
gene: POLR2C was added to Congenital hypothyroidism. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: POLR2C.
Mode of inheritance for gene: POLR2C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: POLR2C were set to 34794894; 29367954
Phenotypes for gene: POLR2C were set to Primary ovarian insufficiency