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Prepair 1000+

Gene: OPN1LW

Red List (low evidence)

OPN1LW (opsin 1, long wave sensitive)
EnsemblGeneIds (GRCh38): ENSG00000102076
EnsemblGeneIds (GRCh37): ENSG00000102076
OMIM: 300822, Gene2Phenotype
OPN1LW is in 4 panels

0 reviews

Details

Mode of Inheritance
X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Mackenzie's Mission
Phenotypes
  • Blue cone monochromacy, MIM#303700
  • Colorblindness, protan, MIM#303900
OMIM
300822
Clinvar variants
Variants in OPN1LW
Penetrance
None
Panels with this gene

History Filter Activity

1 Jun 2022, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: OPN1LW was added gene: OPN1LW was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Red Mode of inheritance for gene: OPN1LW was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Phenotypes for gene: OPN1LW were set to Blue cone monochromacy, MIM#303700; Colorblindness, protan, MIM#303900