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Craniosynostosis v1.29 CYP26B1 Zornitza Stark Phenotypes for gene: CYP26B1 were changed from 614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES to Craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies, MIM# 614416
Craniosynostosis v0.25 CYP26B1 Tiong Tan Marked gene: CYP26B1 as ready
Craniosynostosis v0.25 CYP26B1 Tiong Tan Gene: cyp26b1 has been classified as Green List (High Evidence).
Craniosynostosis v0.25 CYP26B1 Tiong Tan Classified gene: CYP26B1 as Green List (high evidence)
Craniosynostosis v0.25 CYP26B1 Tiong Tan Gene: cyp26b1 has been classified as Green List (High Evidence).
Craniosynostosis v0.24 CYP26B1 Tiong Tan gene: CYP26B1 was added
gene: CYP26B1 was added to Craniosynostosis. Sources: Literature
Mode of inheritance for gene: CYP26B1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CYP26B1 were set to 27410456; 22019272
Phenotypes for gene: CYP26B1 were set to 614416 RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES
Penetrance for gene: CYP26B1 were set to Complete
Review for gene: CYP26B1 was set to GREEN
Added comment: Three unrelated families in two publications, the first of which also demonstrated robust functional work in murine embryos, zebrafish and in vitro assays suggesting aberrant osteoblast-osteocyte transition.
Sources: Literature