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Fetal anomalies v0.4315 COPB2 Zornitza Stark Marked gene: COPB2 as ready
Fetal anomalies v0.4315 COPB2 Zornitza Stark Gene: copb2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.4315 COPB2 Zornitza Stark Classified gene: COPB2 as Red List (low evidence)
Fetal anomalies v0.4315 COPB2 Zornitza Stark Gene: copb2 has been classified as Red List (Low Evidence).
Fetal anomalies v0.4266 COPB2 Ain Roesley gene: COPB2 was added
gene: COPB2 was added to Fetal anomalies. Sources: Literature
Mode of inheritance for gene: COPB2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: COPB2 were set to 29036432; 34450031
Phenotypes for gene: COPB2 were set to Microcephaly 19, primary, autosomal recessive, MIM# 617800
Review for gene: COPB2 was set to RED
gene: COPB2 was marked as current diagnostic
Added comment: IUGR or small at birth (including microcephaly) not noted for any of the probands. Fractures and osteopenia were not detected antenatally.
Sources: Literature