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Callosome v0.215 NR2F1 Zornitza Stark Marked gene: NR2F1 as ready
Callosome v0.215 NR2F1 Zornitza Stark Gene: nr2f1 has been classified as Red List (Low Evidence).
Callosome v0.215 NR2F1 Zornitza Stark Phenotypes for gene: NR2F1 were changed from to Bosch-Boonstra-Schaaf optic atrophy syndrome, MIM# 615722
Callosome v0.214 NR2F1 Zornitza Stark Publications for gene: NR2F1 were set to
Callosome v0.213 NR2F1 Zornitza Stark Mode of inheritance for gene: NR2F1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.212 NR2F1 Zornitza Stark Classified gene: NR2F1 as Red List (low evidence)
Callosome v0.212 NR2F1 Zornitza Stark Gene: nr2f1 has been classified as Red List (Low Evidence).
Callosome v0.211 NR2F1 Zornitza Stark reviewed gene: NR2F1: Rating: RED; Mode of pathogenicity: None; Publications: 32275123; Phenotypes: Bosch-Boonstra-Schaaf optic atrophy syndrome, MIM# 615722; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Callosome v0.0 NR2F1 Zornitza Stark gene: NR2F1 was added
gene: NR2F1 was added to Corpus callosum agenesis, Callosome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: NR2F1 was set to Unknown