WormMine

WS294

Intermine data mining platform for C. elegans and related nematodes

Gene :

WormBase Gene ID  ? WBGene00303000 Gene Name  C37C3.18
Sequence Name  ? C37C3.18 Organism  Caenorhabditis elegans
Automated Description  Predicted to enable translation initiation factor activity. Predicted to be involved in translational initiation. Biotype  SO:0001217
Genetic Position  V:± Length (nt)  ? 1063
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1 Organism

Name Taxon Id
Caenorhabditis elegans 6239

1 Synonyms

Value
WBGene00303000

Genomics

2 Transcripts

WormMine ID Sequence Name Length (nt) Chromosome Location
Transcript:C37C3.18a.1 C37C3.18a.1 333   V: 7854993-7856015
Transcript:C37C3.18b.1 C37C3.18b.1 383   V: 7854993-7856055
 

Other

2 CDSs

WormMine ID Sequence Name Length (nt) Chromosome Location
CDS:C37C3.18a C37C3.18a 255   V: 7855052-7855115
CDS:C37C3.18b C37C3.18b 234   V: 7855052-7855115

1 RNAi Result

WormBase ID
WBRNAi00029635

20 Allele

Public Name
gk963301
gk963553
gk964259
gk964351
gk963850
gk962860
gk240229
gk240230
gk240231
gk240232
gk240233
gk240234
ttTi4440
WBVar00213177
gk736030
gk314698
gk729101
gk908134
gk751546
gk559311

1 Chromosome

WormBase ID Organism Length (nt)
V Caenorhabditis elegans 20924180  

1 Chromosome Location


Feature . Primary Identifier
Start End Strand
WBGene00303000 7854993 7856055 1

3 Data Sets

Name URL
WormBaseAcedbConverter  
GO Annotation data set  
C. elegans genomic annotations (GFF3 Gene)  

0 Downstream Intergenic Region

4 Expression Clusters

Regulated By Treatment Description Algorithm Primary Identifier
  Transcripts that showed significantly increased expression in L1 neural cells comparing to in adult neural cells. DESeq2 (v1.18.1) fold change > 2, P-adj<0.05, using BenjaminiHochberg correction. WBPaper00060811:L1_vs_adult_upregulated_neural
  Proteins interacting with NHR-49-GFP according to co-IP and LC-MS. N.A. WBPaper00064071:NHR-49_interacting
  Genes with differential expression under 0.5mg/l Diazinon (DZN) treatment at 24 centigrade. To identify the differentially expressed genes in each treatment authors used linear models per toxicant and temperature (gene expression = Toxicant (effect) + error). The lm function in R stats package was used to implement the linear models analysis with recommended default options. For threshold determination authors used a permutation approach. For each of the 23,232 permutations used authors randomly picked a transcript (array spot), which could only be picked once. Authors combined all the expression values of this transcript and randomly distributed them over the replicates and used them in the linear model. In this way authors obtained a threshold for each of the toxicants. Authors used a -log10 p-value 2 as common threshold for the analysis, which resembles to the following FDR per toxicant: 0.0155 for CPF at 24 centigrade, 0.0148 for DZN at 24 centigrade, 0.0168 for CPF+DZN at 24 centigrade, 0.0142 for CPF at 16 centigrade, 0.0151 for DZN at 16 centigrade, and 0.0148 for CPF+DZN, at 16 centigrade. WBPaper00040210:Diazinon_24C_regulated
  Proteins that interact with HMG-3-HA in BAT1753 [hmg-3(bar24[hmg-3-3xHA]) I] at L4 larva stage according to Co-Immunoprecipitation with subsequent Mass Spectrometry analysis. N.A. WBPaper00055013:HMG-3_interacting_protein

0 Expression Patterns

2 GO Annotation

Annotation Extension Qualifier
  involved_in
  enables

0 Homologues

1 Locations


Feature . Primary Identifier
Start End Strand
WBGene00303000 7854993 7856055 1

2 Ontology Annotations

Annotation Extension Qualifier
  involved_in
  enables

0 Regulates Expr Cluster

1 Sequence

Length
1063

1 Sequence Ontology Term