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C19ORF20-PRKACA Fusion FISH Probe

The C19ORF20-PRKACA Fusion FISH Probe is used to confirm a fusion of the C19ORF20 and PRKACA genes. The fusion of the C19ORF20 and PRKACA genes has been associated with Breast Invasive Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
C19ORF20-PRKACA-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-RERE 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-REOR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-REGO 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-REGR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-REAQ 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-ORRE 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-OROR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-ORGO 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-ORAQ 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GORE 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GOOR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GOGO 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GOGR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GOAQ 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GRRE 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GROR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GRGO 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GRGR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-GRAQ 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-AQRE 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-AQOR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-AQGO 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-AQGR 20 (40 μL) 200 μL
C19ORF20-PRKACA-20-AQAQ 20 (40 μL) 200 μL

PRKACA Gene Summary

This gene encodes one of the catalytic subunits of protein kinase A, which exists as a tetrameric holoenzyme with two regulatory subunits and two catalytic subunits, in its inactive form. cAMP causes the dissociation of the inactive holoenzyme into a dimer of regulatory subunits bound to four cAMP and two free monomeric catalytic subunits. Four different regulatory subunits and three catalytic subunits have been identified in humans. cAMP-dependent phosphorylation of proteins by protein kinase A is important to many cellular processes, including differentiation, proliferation, and apoptosis. Constitutive activation of this gene caused either by somatic mutations, or genomic duplications of regions that include this gene, have been associated with hyperplasias and adenomas of the adrenal cortex and are linked to corticotropin-independent Cushing's syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. Tissue-specific isoforms that differ at the N-terminus have been described, and these isoforms may differ in the post-translational modifications that occur at the N-terminus of some isoforms. [provided by RefSeq, Jan 2015]

Gene Name: Protein Kinase CAMP-activated Catalytic Subunit Alpha

Chromosome: CHR19: 14202506 -14228559

Locus: 19p13.12

Gene Diseases

The C19ORF20 PRKACA Fusion has been associated with the following diseases:

Disease Name
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

DNAJB1-PRKACA fusions occur in oncocytic pancreatic and biliary neoplasms and are not specific for fibrolamellar hepatocellular carcinoma

A new DNAJB1-PRKACA fusion was recently discovered in fibrolamellar hepatocellular carcinoma (FHCC). This study sought to determine the specificity of this fusion for the disease through molecular and genetic analysis of six PRKACA-rearranged pancreatobiliary neoplasms. Empire Genomics’ PRKACA break apart FISH probe was used to detect PRKACA rearrangements in the tumors. Five cases were found to have DNAJB1-PRKACA fusions and one had ATP1B1-PRKACA fusion.