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24 Mar 2019	Fetal anomalies v0.134	MAB21L2	Rebecca Foulger edited their review of gene: MAB21L2: Added comment: This gene and phenotype were reviewed during meetings at Great Ormond Street hospital in March 2019. Clinical review and curation was performed by Lyn Chitty, Anna de Burca, Rhiannon Mellis, Richard Scott, Ellen McDonagh and Rebecca Foulger. Outcome of review: Confirmed that phenotype is fetally-relevant: keep on the Fetal anomalies panel as a Green gene.; Changed rating: GREEN
11 Dec 2018	Fetal anomalies v0.9	MAB21L2	Rebecca Foulger commented on gene: MAB21L2: DDG2P rating in original PAGE list: Confirmed for MICROPHTHALMIA, SYNDROMIC 14
08 Nov 2018	Fetal anomalies v0.3	MAB21L2	Rebecca Foulger reviewed gene: MAB21L2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
08 Nov 2018	Fetal anomalies v0.1	MAB21L2	Rebecca Foulger Added phenotypes MICROPHTHALMIA, SYNDROMIC 14 for gene: MAB21L2
08 Nov 2018	Fetal anomalies v0.1	MAB21L2	Rebecca Foulger gene: MAB21L2 was added gene: MAB21L2 was added to Fetal anomalies. Sources: Expert Review Green,PAGE DD-Gene2Phenotype Mode of inheritance for gene: MAB21L2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Phenotypes for gene: MAB21L2 were set to MICROPHTHALMIA, SYNDROMIC 14