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WormBase Tree Display for Gene: WBGene00001371

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Name Class

WBGene00001371EvidencePerson_evidenceWBPerson260
SMapS_parentSequenceF26H11
IdentityVersion1
NameCGC_nameexl-1Person_evidenceWBPerson260
Sequence_nameF26H11.5
Molecular_nameF26H11.5
F26H11.5.1
CE24922
Other_nameCELE_F26H11.5Accession_evidenceNDBBX284602
Public_nameexl-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:24WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classexl
Allele (33)
StrainWBStrain00031671
RNASeq_FPKM (74)
GO_annotation (29)
Ortholog (47)
ParalogWBGene00001365Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001790Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001791Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001792Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008920Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015337Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00016204Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019636Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021817Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00043097Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionexl-1 encodes a putative chloride intracellular channel (CLIC) paralogous to EXC-4; transgenic EXL-1 can partially rescue the exc-4(rh133) mutant phenotype when its expression is driven with an exc-4 promoter; EXL-1 is localized to lysosomes in intestinal cells and coelomocytes, endoplasmic reticulum in coelomocytes, Golgi apparatus in muscle and the neurons PVD and CAN, plasma membrane in muscle arms, and to dense bodies linking muscle cytoskeleton to hypodermis through muscle cell membranes; EXL-1 has an N-terminal PTM domain required for its membrane targeting, and a C-terminal domain resembling omega-type glutathione-S-transferases; EXL-1 has no known function in vivo, and exl-1(ok857) mutants have no obvious phenotype.Paper_evidenceWBPaper00006263
WBPaper00027655
Curator_confirmedWBPerson567
Date_last_updated18 Jan 2008 00:00:00
Automated_descriptionPredicted to enable chloride channel activity. Predicted to be involved in chloride transport. Located in apical plasma membrane; cytoplasm; and muscle cell projection membrane. Expressed in coelomocyte; intestine; muscle cell; and neurons. Used to study alcohol use disorder. Human ortholog(s) of this gene implicated in X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome. Is an ortholog of human CLIC2 (chloride intracellular channel 2) and CLIC4 (chloride intracellular channel 4).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
Disease_infoExperimental_modelDOID:1574Homo sapiensPaper_evidenceWBPaper00040625
Curator_confirmedWBPerson324
Date_last_updated29 Apr 2019 00:00:00
Potential_modelDOID:0060828Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2063)
Models_disease_assertedWBDOannot00000653
Molecular_infoCorresponding_CDSF26H11.5
Corresponding_transcriptF26H11.5.1
Other_sequenceTcol_isotig00207
CBC02920_1
FD517449.1
CSC01417_1
Associated_featureWBsf666366
WBsf666367
WBsf666368
WBsf990706
WBsf1013839
WBsf224272
Experimental_infoRNAi_resultWBRNAi00031474Inferred_automaticallyRNAi_primary
WBRNAi00013985Inferred_automaticallyRNAi_primary
WBRNAi00045703Inferred_automaticallyRNAi_primary
WBRNAi00090593Inferred_automaticallyRNAi_primary
Expr_patternExpr2810
Expr9874
Expr1015562
Expr1030826
Expr1149614
Expr2011395
Expr2029631
Drives_constructWBCnstr00010963
WBCnstr00012955
WBCnstr00014373
WBCnstr00015737
WBCnstr00036986
Construct_productWBCnstr00010963
WBCnstr00012955
WBCnstr00014373
WBCnstr00015737
WBCnstr00036986
Microarray_results (17)
Expression_cluster (121)
Interaction (19)
Map_infoMapIIPosition22.9676Error0.006188
PositivePositive_cloneF26H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4590
Pseudo_map_position
Reference (12)
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene