PrimePCR™ Probe Assay: RHO, Human

RT

Real-time PCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

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Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCIP0030630
Assay Design:   Intron-spanning
Chromosome Location:   3:129247854-129249788question
Amplicon Length:   124
Splice Variants Targeted:   ENST00000296271

Gene Information

Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant autosomal recessive or X-linked recessive disorder. In the autosomal dominant formwhich comprises about 25% of total cases approximately 30% of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which when photoexcited initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness. [provided by RefSeq Jul 2008]

Gene Symbol:   RHO
Gene Name:   rhodopsin
Aliases:   CSNBAD1, MGC138309, MGC138311, OPN2, RP4
RefSeq:   NC_000003.11 NG_009115.1 NT_005612.16
Ensembl:   ENSG00000163914
Entrez:   6010
Chromosome Mapping:   3q21-q24

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