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RNAi Experiment: [pmid12181365]:PEX13 Ace View of [pmid12181365]:PEX13
Genes Inhibited How is RNAi inhibition determined?
Gene Inhibited  F32A5.6 (prx-13)
Description of "F32A5.6"  prx-13 is orthologous to the human gene PEX13 (OMIM:601789), which when mutated leads to Zellweger syndrome or neonatal adrenoleukodystrophy.
KOG Annotation  Peroxisomal biogenesis protein peroxin
What's a KOG?
Evidence for Inhibition 
ePCR Status: Unique_ePCR (II:7250171..7251296)
Transcript overlap: 844 nt		 Explain types of evidence for RNAi inhibition
Sliding Window Raw score: 760
Relative score: 1 (This gene has the best score for this RNAi reagent)
Specificity index: 1 (RNAi reagent is specific for this gene)
Wormbase (BLAST) RNAi primary
External "F32A5.6" Links  Wormbase NCBI
[pmid12181365]:PEX13 Phenotypes Help with Phenotypes
Larval  Lva
Phenotype  Unclassified a diffuse pattern of fluorescence of CFP-SKL (ser-lys-leu), characteristic of the cytosol, was observed, suggesting a deficiency in the peroxisomal import of PTS1-targeted matrix proteins
[pmid12181365]:PEX13 Experiment Details Ace View
RNAi Reagent & Type  [pmid12181365]:PEX13 (PCR_reagent)
Reference  Petriv OI et al. (2002) Physiological Genomics "RNA interference of peroxisome-related genes in C. elegans: a new model for human ...."
Delivery Method  Injection
Date  2002-8-14
Gene Plot of F32A5.6 Browse using GBrowse
Gene Graph