WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Gene :

WormBase Gene ID  ? WBGene00195017 Gene Name  srpr-2.2
Sequence Name  ? R144.15 Organism  Caenorhabditis elegans
Automated Description  Enriched in NSM; anchor cell; sensory neurons; and ut4 based on RNA-seq and single-cell RNA-seq studies. Is affected by several genes including crh-1; hpl-2; and unc-30 based on RNA-seq and microarray studies. Is affected by Ethanol; Tunicamycin; and paraquat based on RNA-seq studies. Biotype  SO:0001263
Genetic Position  III :-2.21008± Length (nt)  ? 299
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1 Organism

Name Taxon Id
Caenorhabditis elegans 6239

1 Synonyms

Value
WBGene00195017

Genomics

1 Transcripts

WormMine ID Sequence Name Length (nt) Chromosome Location
Transcript:R144.15 R144.15 299   III: 5031410-5031708
 

Other

0 CDSs

4 RNAi Result

WormBase ID
WBRNAi00038863
WBRNAi00009661
WBRNAi00007067
WBRNAi00034932

11 Allele

Public Name
gk964504
tm8587
gk964503
gk173888
gk500631
gk173887
gk549136
ok1869
gk351505
gk374445
gk883296

1 Chromosome

WormBase ID Organism Length (nt)
III Caenorhabditis elegans 13783801  

1 Chromosome Location


Feature . Primary Identifier
Start End Strand
WBGene00195017 5031410 5031708 -1

2 Data Sets

Name URL
WormBaseAcedbConverter  
C. elegans genomic annotations (GFF3 Gene)  

0 Downstream Intergenic Region

30 Expression Clusters

Regulated By Treatment Description Algorithm Primary Identifier
Osmotic stress Transcripts that showed significantly altered expression with 500 mM salt (NaCl) vs 100 mM salt when food was present DESeq(version 1.10.1), FDR < 0.05. WBPaper00050726:OsmoticStress_regulated_Food
  Genes significantly enriched in NSM neurons (isolated by FACS) versus the reference, according to RNAseq analysis towards total RNA. Gene expression quantification and differential expression was analyzed using cufflinks v2.2.1. Enriched contains only genes significantly enriched (differentially expressed >= 2.4 fold in total RNA or >= 3.2 fold in DSN treated total RNA) in the NSM neurons versus the reference. WBPaper00045974:NSM_enriched_totalRNA_RNAseq
  Transcripts that showed significantly decreased expression in N2 animals exposed to 0.1mM Paraquat from hatching to reaching adult stage. DESeq2 version 1.22.2, p < 0.05 WBPaper00064716:paraquat_downregulated
  Transcripts depleted in purified oocyte P bodies comparing to in whole oocytes. DESeq2, FDR < 0.05, fold change > 2. WBPaper00065975:P-body_vs_oocyte_depleted
  Transcripts depleted in purified oocyte P bodies comparing to in the whole animal. DESeq2, FDR < 0.05, fold change > 2. WBPaper00065975:P-body_vs_WholeAnimal_depleted
  Transcripts that showed significantly increased expression in 10-days post L4 adult hermaphrodite N2 grown at 20C, comparing to in 1-day post L4 adult hermaphrodite N2 animals grown at 20C. CuffDiff, fold change > 2. WBPaper00065096:Day10_vs_Day1_upregulated
  Transcripts that showed significantly increased expression in daf-2(e1370) comparing to in N2. Differential gene expression analysis was performed using the quasi-likeli-hood framework in edgeR package v. 3.20.1 in R v. 3.4.1. WBPaper00053810:daf-2(e1370)_upregulated
  Transcripts that showed significantly decreased expression in hpl-2(tm1489) comparing to in N2 animals. DESeq2, adjusted p-value < 0.05, log2 fold change > 2 or < -2. WBPaper00054493:hpl-2(tm1489)_downregulated
  Transcripts that showed significantly increased expression in ilc-17.1(syb5296) comparing to in N2 animals at L4 larva stage. DESeq2, fold change > 2, FDR < 0.05. WBPaper00066594:ilc-17.1(syb5296)_upregulated
  Transcripts that showed significantly increased expression in animals lacking P granules by RNAi experiments targeting pgl-1, pgl-3, glh-1 and glh-4, and unc-119-GFP(+), comparing to in control animals, at 2-day post L4 adult hermaphrodite stage. DESeq2, Benjamini-Hochberg multiple hypothesis corrected p-value < 0.05 and fold change > 2. WBPaper00050859:upregulated_P-granule(-)GFP(+)_vs_control_day2-adult
  Transcripts that showed significantly increased expression in unc-30(ok613) animals at L4 larva stage, comparing to N2 animals. Genes exhibiting at least two-fold change were considered differentially expressed. WBPaper00061439:unc-30(ok613)_upregulated
  Transcripts that showed significantly increased expression in pmt-2(RNAi) animals comparing to control animals iinjected with empty vector. Fold-change > 1.5, ANOVA P values < 0.05. WBPaper00055482:pmt-2(RNAi)_upregulated
  Transcripts that interact with 3xFLAG-DLC-1 as identified by immunoprecipitation followed by RNA sequencing. DESeq2, fold change > 2,, p-value < 0.01 WBPaper00055334:DLC-1_interacting
  Transcripts that showed significantly decreased expression in lin-53(RNAi) embryos comparing to control animals. DESeq2, fold change > 2, FDR < 0.05. WBPaper00067044:lin-53(RNAi)_downregulated
  Transcripts enriched in invading anchor cells comparing to in whole animal. DESeq2v.1.30.1. fold change >= 2, FDR < 0.05 WBPaper00065258:anchor-cell_enriched
  Transcripts that showed significantly decreased expression in hda-1(RNAi) embryos comparing to control animals. DESeq2, fold change > 2, FDR < 0.05. WBPaper00067044:hda-1(RNAi)_downregulated
heat-killed OP50 Transcripts that showed significantly increased expression in N2 L1 animals fed with heat-killed OP50 for 4 hours comparing to those animals fed with OP50. DESeq2, fold change > 2, FDR < 0.05. WBPaper00067214:Heat-Killed-OP50_upregulated
  Transcripts that showed significantly increased expression in sensory neuron (labeled by iaIs25[Pgcy-37::GFP + unc-119(+)]) comparing to in whole worm. Fold change > 2, p-value < 0.05. WBPaper00060661:sensory-neuron_enriched
  Transcripts that showed significantly increased expression in mbl-1(tm1563) comparing to in N2 animals. Differential expression analysis was performed using the EdgeR package after normalizing read counts and including only those genes with CPM > 1 for at least one out of all samples. WBPaper00062167:mbl-1(tm1563)_upregulated
  Transcripts that showed differential expression between 24 and 26 hours post hatching L2d and dauer committed larvae of daf-9(dh6), triggered by the dafachronic acid (DA) growth hormone. Cluster 6 genes increased expression in L4. Benjamini Hochberg corrected q-value < 0.01. WBPaper00053388:dauer_regulated_Cluster6
  Genes that are upregulated by 0.2M ethanol treatment. Differences in gene expression levels between the two groups of worms were analyzed with Cufflinks 1.0.3, using a cutoff of twofold difference and FDR corrected p < 0.05. WBPaper00041954:ethanol_upregulated
  Transcripts that showed significantly decreased expression in H3.3 null mutant animals (FAS43 [his-69&his-70(uge44) III; his-72(tm2066) III; his-74(uge18) V; his-71(ok2289) X]) comparing to in N2 animals at L1 larva stage. Differentially expressed genes were estimated using a General Linear Model approach, negative binomial distribution, and a quasi-likelihood F-test. Genes with a P-value < 0.05 and fold change > 1 were considered significant. WBPaper00054191:H3.3(null)_L1_downregulated
  Transcripts with significantly increased expression in egl-9(sa307) comparing to in N2. Bioconductor's edgeR package in the R 3.2.3, adjusted p value < 0.05. WBPaper00054872:egl-9(sa307)_upregulated
  Transcripts that showed significantly decreased expression in animals overexpression human amylin (driven by hsp-16.2). Differential gene expression analysiswas conducted using the DESeq R package (available from Bio-conductor). The DESeq analysis resulted in the determination of potential differentially expressed genes when compared between the DMH46 and N2 (wildtype) samples. The read counts for each sample were normalized for sequencing depth and distortion caused by highly differentially expressed genes.Then the negative bi nomial (NB) model was used to test the significance of differential expression between two genotypes.The differentially expressed genes were deemed significant if the FDR (False Discovery Rate) was less than 0.05, and the gene expression was above the 10th percentile, and showed greater than 2-fold change difference(overexpressed or underexpressed) between the conditions. WBPaper00056731:human-amylin_downregulated
  Transcripts that showed significantly decreased expression after daf-22(ok693) L1 larva animals were exposed to 150uL of an ascaroside cocktail made of equal amounts (50uL) of 33uM synthetic ascr#2, ascr#3, and ascr#8 in ethanol, comparing to control animals exposed to 150uL EtOH. DESeq fold change > 2, p < 0.001. WBPaper00061390:daf-22(ok693)_ascarosides_downregulated
  Transcripts that showed significantly increased expression in uaf-1(n4588) comparing to in N2 at embryo stage. DEGSeq 1.18.0, p < 0.05, fold change > 2. WBPaper00055364:uaf-1(n4588)_upregulated
  Transcripts that showed significantly increased expression after 4 hours of treatment by 50 ub per ml tunicamycin at L4 larva stage, in RtcB(null) animals. Fold change > 1.75 WBPaper00045971:tunicamycin_upregulated_RtcB(null)
  Single-cell RNA-Seq cell group 13_1 expressed in epithelium. scVI 0.6.0 WBPaper00065841:13_1
  Transcripts significantly downregulated in crh-1(n3315) vs N2 hypodermal tissue. DESeq2, FDR < 0.05. WBPaper00059816:crh-1(n3315)_downrgulated
Radiation: below underground radiation at Waste Isolation Pilot Plant (WIPP), a nuclear waste disposal site operated by the United StatesDepartment of Energy located 42 km east of Carlsbad, NM. Transcripts that showed significantly increased expression among animals grown underground surrounded by nuclear waste radiation, comparing to animals protected with plexiglass panels filled withKCl (surrogate for normal background radiation) or NaCl (lowradiation group). Differential gene expression was identified by Partek GSA algorithm. WBPaper00060744:Radiation_upregulated

0 Expression Patterns

0 GO Annotation

0 Homologues

1 Locations


Feature . Primary Identifier
Start End Strand
WBGene00195017 5031410 5031708 -1

0 Ontology Annotations

0 Regulates Expr Cluster

1 Sequence

Length
299

1 Sequence Ontology Term