Gene:  NYX, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair gene expression assay target

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The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1) also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision myopia hyperopia nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq Oct 2008]

PrimePCR™ SYBR® Green Assay: NYX, Human
nyctalopin

Assay Type: SYBR® Green
Assay Design: Exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0004654
List Price:    $174.00
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PrimePCR™ SYBR® Green Assay: NYX, Human
nyctalopin

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0048008
Info:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0055268
List Price:    $174.00
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PrimePCR™ Probe Assay: NYX, Human
nyctalopin

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0055268
List Price:    $255.00
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    Related pathways not available
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