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Retinal disorders v1.159 OPN1LW Gavin Arno reviewed gene: OPN1LW: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Retinal disorders v1.154 OPN1LW Ivone Leong Publications for gene: OPN1LW were set to
Retinal disorders v1.153 OPN1LW Ivone Leong Classified gene: OPN1LW as Green List (high evidence)
Retinal disorders v1.153 OPN1LW Ivone Leong Added comment: Comment on list classification: Promoted from red to green. This gene is associated with a phenotype on OMIM but not Gene2Phenotype. There are >3 unrelated cases reported on OMIM; therefore, there is enough evidence to promote this gene to green status.
Retinal disorders v1.153 OPN1LW Ivone Leong Gene: opn1lw has been classified as Green List (High Evidence).
Retinal disorders v1.152 OPN1LW Ivone Leong Phenotypes for gene: OPN1LW were changed from to Blue cone monochromacy, 303700
Retinal disorders v1.151 OPN1LW Ivone Leong Mode of inheritance for gene: OPN1LW was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Retinal disorders v1.137 OPN1LW Ivone Leong Source NHS GMS was added to OPN1LW.
Retinal disorders OPN1LW BRIDGE consortium reviewed OPN1LW