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WormBase Tree Display for Gene: WBGene00000532

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Name Class

WBGene00000532SMapS_parentSequenceCHROMOSOME_II
IdentityVersion1
NameCGC_nameclh-5
Sequence_nameC07H4.2
Molecular_nameC07H4.2
C07H4.2.1
CE27360
Other_nameCELE_C07H4.2Accession_evidenceNDBBX284602
Public_nameclh-5
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classclh
Allele (64)
StrainWBStrain00001511
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (45)
ParalogWBGene00000533Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00000528Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000529Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000530Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000531Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionThe clh-5 gene encodes a chloride channel, whose human homologs include CLC1 and CLCN5; the latter homolog is imvolved in receptor-mediated endocytosis.Paper_evidenceWBPaper00004103
WBPaper00004883
WBPaper00012835
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable voltage-gated chloride channel activity. Predicted to be involved in chloride transmembrane transport. Predicted to be located in Golgi apparatus; early endosome; and synaptic vesicle. Expressed in several structures, including head and tail. Human ortholog(s) of this gene implicated in Raynaud-Claes syndrome and X-linked recessive disease (multiple). Is an ortholog of human CLCN4 (chloride voltage-gated 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_infoPotential_modelDOID:0111815Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2023)
DOID:0050699Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2023)
DOID:0112060Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2022)
DOID:0111798Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2023)
DOID:0080353Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2023)
Molecular_infoCorresponding_CDSC07H4.2
Corresponding_CDS_historyC07H4.2:wp48
Corresponding_transcriptC07H4.2.1
Other_sequence (49)
Associated_featureWBsf223603
Experimental_infoRNAi_resultWBRNAi00062113Inferred_automaticallyRNAi_primary
WBRNAi00086835Inferred_automaticallyRNAi_primary
WBRNAi00065615Inferred_automaticallyRNAi_primary
WBRNAi00040037Inferred_automaticallyRNAi_primary
WBRNAi00028650Inferred_automaticallyRNAi_primary
WBRNAi00077549Inferred_automaticallyRNAi_primary
WBRNAi00010411Inferred_automaticallyRNAi_primary
Expr_patternChronogram1083
Expr1126
Expr5200
Expr1027246
Expr1030318
Expr1144107
Expr2010232
Expr2028474
Drives_constructWBCnstr00002368
WBCnstr00010094
WBCnstr00037468
Construct_productWBCnstr00037468
Microarray_results (21)
Expression_cluster (103)
Interaction (31)
Map_infoMapIIPosition1.01436Error0.007131
PositivePositive_cloneC07H4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4337
5255
5491
Pseudo_map_position
Reference (17)
Remarksequence connection from [George AL]
Map 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