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ROM1

retinal outer segment membrane protein 1

HCNC Approved Symbol
ROM1 (HGNC:10254)
Genomic Coordinates
11:62,613,257 - 62,615,116 (11q12.3)
Synonyms
TSPAN23, ROM
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the ROM1 gene.

Frequently observed phenotypes

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

Retinitis pigmentosa
 1 (100.0%)
ROM1 - Gene browser | 3billion