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Mendeliome v0.7056 NMNAT1 Zornitza Stark Mode of inheritance for gene: NMNAT1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.7055 NMNAT1 Zornitza Stark Phenotypes for gene: NMNAT1 were changed from to Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, and Leber congenital amaurosis (SHILCA), MIM#619260; Leber congenital amaurosis 9, MIM# 608553
Mendeliome v0.7054 NMNAT1 Zornitza Stark Publications for gene: NMNAT1 were set to
Mendeliome v0.7053 NMNAT1 Zornitza Stark Tag SV/CNV tag was added to gene: NMNAT1.
Tag founder tag was added to gene: NMNAT1.
Mendeliome v0.7053 NMNAT1 Zornitza Stark Marked gene: NMNAT1 as ready
Mendeliome v0.7053 NMNAT1 Zornitza Stark Gene: nmnat1 has been classified as Green List (High Evidence).
Mendeliome v0.7053 NMNAT1 Zornitza Stark reviewed gene: NMNAT1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32533184, 33668384, 22842230, 22842229; Phenotypes: Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, and Leber congenital amaurosis (SHILCA), MIM#619260, Leber congenital amaurosis 9, MIM# 608553; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.0 NMNAT1 Zornitza Stark gene: NMNAT1 was added
gene: NMNAT1 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: NMNAT1 was set to Unknown