PrimePCR™ Probe Assay: WNT4, 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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PrimePCR™ PreAmp for Probe Assay: WNT4, Human
Reaction:     400 reactions
Gene-specific PCR primers for the unbiased preamplification of small quantities of cDNA for subsequent use in downstream gene expression analysis.

PrimePCR™ Template for Probe Assay: WNT4, Human
Reaction:     200 x 20 µl reactions
Gene-specific synthetic DNA template designed to give a positive real-time PCR result when used with the corresponding probe assay.


Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0025004
Assay Design:   Exonic
Chromosome Location:   1:22456200-22456306question
Amplicon Length:   77
Splice Variants Targeted:   ENST00000290167 ENST00000415567 ENST00000441048 ENST00000542383 ENST00000374655

Gene Information

The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family and is the first signaling molecule shown to influence the sex-determination cascade. It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat. This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation. This gene and another two family members WNT2 and WNT7B may be associated with abnormal proliferation in breast tissue. Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome. [provided by RefSeq Jul 2008]

Gene Symbol:   WNT4
Gene Name:   wingless-type MMTV integration site family, member 4
Aliases:   SERKAL, WNT-4
RefSeq:   NC_000001.10 NG_008974.1 NT_004610.19
Ensembl:   ENSG00000162552
Entrez:   54361
Chromosome Mapping:   1p36.23-p35.1

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