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Mendeliome v2.0 MAB21L1 Gene migrated from ENSG00000180660 to ENSG00000180660 (gene set migration)
Mendeliome v1.4938 MAB21L1 Zornitza Stark Phenotypes for gene: MAB21L1 were changed from Cerebellar, ocular, craniofacial, and genital syndrome #MIM 618479 to Cerebellar, ocular, craniofacial, and genital syndrome #MIM 618479; Microphthalmia MONDO:0021129, MAB21L1-related
Mendeliome v1.4937 MAB21L1 Zornitza Stark Publications for gene: MAB21L1 were set to 30487245
Mendeliome v1.4936 MAB21L1 Zornitza Stark Mode of inheritance for gene: MAB21L1 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendeliome v1.4935 MAB21L1 Zornitza Stark reviewed gene: MAB21L1: Rating: GREEN; Mode of pathogenicity: None; Publications: 39016008, 36892533, 36446583, 36413568; Phenotypes: Microphthalmia MONDO:0021129, MAB21L1-related; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.1023 MAB21L1 Zornitza Stark Marked gene: MAB21L1 as ready
Mendeliome v0.1023 MAB21L1 Zornitza Stark Gene: mab21l1 has been classified as Green List (High Evidence).
Mendeliome v0.1017 MAB21L1 Sue White Classified gene: MAB21L1 as Green List (high evidence)
Mendeliome v0.1017 MAB21L1 Sue White Gene: mab21l1 has been classified as Green List (High Evidence).
Mendeliome v0.1016 MAB21L1 Sue White gene: MAB21L1 was added
gene: MAB21L1 was added to Mendeliome. Sources: Literature
Mode of inheritance for gene: MAB21L1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MAB21L1 were set to 30487245
Phenotypes for gene: MAB21L1 were set to Cerebellar, ocular, craniofacial, and genital syndrome #MIM 618479
Penetrance for gene: MAB21L1 were set to Complete
Review for gene: MAB21L1 was set to GREEN
Added comment: Sources: Literature