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WormBase Tree Display for Gene: WBGene00000531

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Name Class

WBGene00000531SMapS_parentSequenceT06F4
IdentityVersion1
NameCGC_nameclh-4
Sequence_nameT06F4.2
Molecular_nameT06F4.2a
T06F4.2a.1
CE38544
T06F4.2b
CE28648
T06F4.2b.1
Other_nameT06F4.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
T06F4.bCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_T06F4.2Accession_evidenceNDBBX284606
Public_nameclh-4
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classclh
Allele (98)
StrainWBStrain00031843
WBStrain00037721
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (36)
ParalogWBGene00000528Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000529Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000530Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000532Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000533Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable voltage-gated chloride channel activity. Predicted to be involved in chloride transport. Predicted to be located in plasma membrane. Expressed in excretory cell. Human ortholog(s) of this gene implicated in Thomsen disease; idiopathic generalized epilepsy 11; and primary hyperaldosteronism. Is an ortholog of human CLCN1 (chloride voltage-gated channel 1) and CLCN2 (chloride voltage-gated channel 2).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:446Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2020)
DOID:0081336Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2019)
DOID:2106Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2019)
DOID:0111312Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2020)
Molecular_infoCorresponding_CDST06F4.2a
T06F4.2b
Corresponding_CDS_historyT06F4.2a:wp142
Corresponding_transcriptT06F4.2a.1
T06F4.2b.1
Other_sequenceJI171877.1
JI223678.1
Dviv_isotig25055
Tcol_isotig11995
Tcol_isotig11996
HG08696
Acan_isotig12058
Oden_isotig24653
Tcol_isotig18311
HGC03609_1
Associated_feature (11)
Experimental_infoRNAi_resultWBRNAi00035277Inferred_automaticallyRNAi_primary
WBRNAi00018319Inferred_automaticallyRNAi_primary
WBRNAi00052678Inferred_automaticallyRNAi_primary
WBRNAi00077548Inferred_automaticallyRNAi_primary
Expr_patternExpr1125
Expr1190
Expr1010424
Expr1156283
Expr2010231
Expr2028473
Drives_constructWBCnstr00005887
WBCnstr00007706
WBCnstr00010093
WBCnstr00010142
WBCnstr00037469
Construct_productWBCnstr00037469
Microarray_results (25)
Expression_cluster (96)
Interaction (42)
Map_infoMapXPosition-8.50461Error0.115815
PositivePositive_cloneT06F4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5017
Pseudo_map_position
Reference (15)
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