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WormBase Tree Display for Gene: WBGene00017644

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Name Class

WBGene00017644SMapS_parentSequenceF20D12
IdentityVersion3
NameCGC_nameexc-9Person_evidenceWBPerson1052
Sequence_nameF20D12.5
Molecular_nameF20D12.5
F20D12.5.1
CE29767
F20D12.5.2
Other_nametag-291Curator_confirmedWBPerson2970
CELE_F20D12.5Accession_evidenceNDBBX284604
Public_nameexc-9
DB_infoDatabaseAceViewgene4I704
WormQTLgeneWBGene00017644
WormFluxgeneWBGene00017644
NDBlocus_tagCELE_F20D12.5
PanthergeneCAEEL|WormBase=WBGene00017644|UniProtKB=Q19641
familyPTHR24215
NCBIgene177586
RefSeqproteinNM_068925.6
TrEMBLUniProtAccQ19641
UniProt_GCRPUniProtAccQ19641
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
222 Apr 2005 11:55:18WBPerson2970Name_changeCGC_nametag-291
322 Jul 2005 13:21:27WBPerson2970EventAcquires_mergeWBGene00001370
Name_changeCGC_nameexc-9
Other_nametag-291
Acquires_mergeWBGene00001370
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classexc
Allele (16)
Possibly_affected_byWBVar02154074
Legacy_information[Buechner M] Wide, meandering excretory canals, with some septate cysts. Canal enlargement visible from L1 through adult. Defect visible only by Nomarksi microscopy.
Complementation_data[Buechner M] complements exc-5(rh232), exc-5(n2672)
StrainWBStrain00027275
WBStrain00036217
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (30)
ParalogWBGene00003375Caenorhabditis elegansFrom_analysisPanther
WBGene00015216Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000438Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00002987Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00002988Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003000Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003167Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006654Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00006824Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022518Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionexc-9 encodes one of two C. elegans small LIM domain-containing proteins related to the mammalian CRIP (Cysteine-Rich Intestinal Protein) family of proteins; in C. elegans, exc-9 activity is required cell autonomously for proper organization of the apical cytoskeleton of the excretory canal cell, which is essential for maintaining the diameter of the excretory canal tubules; in addition, exc-9 is required for proper morphogenesis of the hermaphrodite and male tails; genetic analyses indicated that exc-9 likely functions upstream of exc-5, which encodes a guanine-nucleotide exchange factor, and downstream of exc-2 and sma-1, in regulating canal cell morphology; an EXC-9::GFP fusion protein is expressed in a number of cell types including the excretory canal cell, the tail spike, the uterine seam cell and anchor cell, the intestine, ALM and PLN neurons, and the nerve ring; in males, EXC-9::GFP expression is seen in a few tail neurons and weakly throughout the tail during larval development; EXC-9::GFP localizes to the cytoplasm; in yeast two-hybrid assays, EXC-9 interacts with CSN-5, a subunit of the COP9 signalosome likely involved in ubiquitin-mediated protein degradation.Paper_evidenceWBPaper00003721
WBPaper00027309
WBPaper00031650
Curator_confirmedWBPerson1843
Date_last_updated18 Nov 2008 00:00:00
Automated_descriptionPredicted to enable zinc ion binding activity. Involved in anatomical structure morphogenesis; epithelial cell development; and regulation of tube size. Located in cytoplasm. Expressed in several structures, including ALM; distal tip cell; excretory canal; lumbar ganglion; and nerve ring. Is an ortholog of human CRIP1 (cysteine rich protein 1).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Molecular_infoCorresponding_CDSF20D12.5
Corresponding_transcriptF20D12.5.1
F20D12.5.2
Other_sequence (69)
Associated_featureWBsf651968
WBsf230357
Transcription_factorWBTranscriptionFactor000457
Experimental_infoRNAi_resultWBRNAi00077722Inferred_automaticallyRNAi_primary
WBRNAi00033560Inferred_automaticallyRNAi_primary
WBRNAi00045105Inferred_automaticallyRNAi_primary
Expr_patternExpr8076
Expr8077
Expr12552
Expr15546
Expr1016400
Expr1149055
Expr2011394
Expr2029630
Drives_construct (12)
Construct_productWBCnstr00013093
Microarray_results (17)
Expression_cluster (180)
Interaction (40)
Map_infoMapIVPosition3.50307Error0.000634
PositivePositive_cloneF20D12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point7084
Multi_point5222
3780
3809
3781
3808
Pos_neg_data10259
10260
10261
10262
Reference (25)
Remarkn2669 was previously listed as an allele of exc-5. Later repeated complementation tests showed n2669 to be an allele of a novel locus positioned close to exc-5.
MethodGene