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Fetal anomalies v0.3732 CDCA8 Zornitza Stark Marked gene: CDCA8 as ready
Fetal anomalies v0.3732 CDCA8 Zornitza Stark Gene: cdca8 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3732 CDCA8 Zornitza Stark Classified gene: CDCA8 as Red List (low evidence)
Fetal anomalies v0.3732 CDCA8 Zornitza Stark Gene: cdca8 has been classified as Red List (Low Evidence).
Fetal anomalies v0.3731 CDCA8 Zornitza Stark reviewed gene: CDCA8: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital hypothyroidism, thyroid dysgenesis, no OMIM #; Mode of inheritance: None
Fetal anomalies v0.3709 CDCA8 Krithika Murali gene: CDCA8 was added
gene: CDCA8 was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: CDCA8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CDCA8 were set to 28025328; 29546359
Phenotypes for gene: CDCA8 were set to Congenital hypothyroidism, thyroid dysgenesis, no OMIM #
Review for gene: CDCA8 was set to GREEN
Added comment: Gene associated with congenital hypothyroidism secondary to thyroid dysgenesis. No new publications since last PanelApp review Feb 2021

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4 families (1 with bilallelic variants [parent affected as HTZ], 3 with monoallelic variants) with functional evidence of variants. GREEN for mono allelic, RED for biallelic.
Sources: Literature