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OPN1MW

opsin 1, medium wave sensitive

HCNC Approved Symbol
OPN1MW (HGNC:4206)
Genomic Coordinates
23:154,182,596 - 154,196,861 (Xq28)
Synonyms
OPN1MW1, COD5, GCP, CBBM, CBD
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Blue cone monochromacy
303700X-linked recessive
Colorblindness, deutan
303800XL

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the OPN1MW gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results