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WormBase Tree Display for Gene: WBGene00000530

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Name Class

WBGene00000530SMapS_parentSequenceE04F6
IdentityVersion1
NameCGC_nameclh-3
Sequence_nameE04F6.11
Molecular_name (28)
Other_namececlc-3Accession_evidenceEMBLAF173172
CELE_E04F6.11Accession_evidenceNDBBX284602
Public_nameclh-3
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classclh
Allele (98)
StrainWBStrain00002629
WBStrain00031612
WBStrain00031617
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (58)
ParalogWBGene00000528Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000529Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000531Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000532Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000533Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionclh-3 encodes a chloride channel homologous to the mammalian channel ClC-2; CLH-3 is expressed in oocytes; CLH-3 carries a hyperpolarization- and swelling-activated Cl(-) current, with biophysical characteristics strongly resembling those of mammalian ClC-2; the CLH-3 current is inactive in immature oocytes, but can be triggered by cell swelling, however, CLH-3 has no obvious role in oocyte volume homeostasis; instead, CLH-3 appears to function as a negative regulator of the gap junction-coupled gonadal sheath cells; the normal physiological time for CLH-3 channel activation is at the onset of oocyte meiotic maturation; inactivation of CLH-3 expression by RNAi causes the gonadal sheath cells, which normally begin contracting during meiotic maturation, to instead begin contractions abnormally early.Paper_evidenceWBPaper00004650
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables voltage-gated chloride channel activity. Involved in chloride transmembrane transport. Located in plasma membrane. Expressed in egg-laying apparatus; epithelial cell; excretory cell; intestine; and muscle cell. Human ortholog(s) of this gene implicated in several diseases, including Thomsen disease; idiopathic generalized epilepsy 11; and renal tubular transport disease (multiple). 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:0050450Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2027)
DOID:2106Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2019)
DOID:10003Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2026)
DOID:0111312Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2020)
DOID:10763Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2027)
DOID:0110144Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2027)
DOID:0081336Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2019)
DOID:0110146Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2026,HGNC:2027)
Molecular_infoCorresponding_CDSE04F6.11a
E04F6.11c
E04F6.11d
E04F6.11e
E04F6.11f
E04F6.11g
E04F6.11h
E04F6.11i
Corresponding_CDS_historyE04F6.11b:wp86
E04F6.11b:wp205
E04F6.11b:wp248
Corresponding_transcript (12)
Other_sequenceOden_isotig25962
JI179920.1
MHC02649_1
MH06173
Acan_isotig13455
FK805027.1
JI180187.1
Oden_isotig18922
Associated_featureWBsf665249
WBsf665678
WBsf223314
WBsf223315
Experimental_infoRNAi_resultWBRNAi00012687Inferred_automaticallyRNAi_primary
WBRNAi00001831Inferred_automaticallyRNAi_primary
WBRNAi00012688Inferred_automaticallyRNAi_primary
WBRNAi00043676Inferred_automaticallyRNAi_primary
WBRNAi00007198Inferred_automaticallyRNAi_primary
WBRNAi00077551Inferred_automaticallyRNAi_primary
WBRNAi00086834Inferred_automaticallyRNAi_primary
Expr_patternChronogram425
Expr1124
Expr1189
Expr2718
Expr1021775
Expr1030317
Expr1147660
Expr2010230
Expr2028472
Drives_constructWBCnstr00003179
WBCnstr00010092
WBCnstr00010140
WBCnstr00018726
WBCnstr00018727
WBCnstr00018728
Construct_productWBCnstr00018726
WBCnstr00018727
WBCnstr00018728
AntibodyWBAntibody00000721
WBAntibody00000884
Microarray_results (30)
Expression_cluster (114)
Interaction (12)
Map_infoMapIIPosition0.499628Error4.8e-05
PositivePositive_cloneE04F6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4568
4615
Pseudo_map_position
Reference (33)
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