Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00000533

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00000533SMapS_parentSequenceR07B7
IdentityVersion2
NameCGC_nameclh-6
Sequence_nameR07B7.1
Molecular_nameR07B7.1
R07B7.1.1
CE29336
Other_namecup-12Paper_evidenceWBPaper00050677
CELE_R07B7.1Accession_evidenceNDBBX284605
Public_nameclh-6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
217 Feb 2017 10:31:31WBPerson2970Name_changeOther_namecup-12
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classclh
Allele (47)
Possibly_affected_byWBVar02158824
StrainWBStrain00031632
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP5320
Ortholog (36)
ParalogWBGene00000532Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00000528Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000529Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000530Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00000531Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable chloride transmembrane transporter activity. Involved in lysosomal protein catabolic process. Predicted to be located in lysosomal membrane. Expressed in several structures, including body wall musculature; head; intestine; non-striated muscle; and tail. Human ortholog(s) of this gene implicated in autosomal dominant osteopetrosis 2 and autosomal recessive osteopetrosis 4. Is an ortholog of human CLCN7 (chloride voltage-gated channel 7).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:0110938Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2025)
DOID:0110944Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2025)
Molecular_infoCorresponding_CDSR07B7.1
Corresponding_CDS_historyR07B7.1:wp63
Corresponding_transcriptR07B7.1.1
Other_sequence (46)
Associated_featureWBsf234613
Experimental_infoRNAi_resultWBRNAi00051426Inferred_automaticallyRNAi_primary
WBRNAi00077550Inferred_automaticallyRNAi_primary
Expr_patternExpr829
Expr830
Expr1127
Expr6473
Expr16466
Expr1013700
Expr1030319
Expr1155115
Expr2010233
Expr2028475
Drives_constructWBCnstr00002568
WBCnstr00010095
WBCnstr00013238
WBCnstr00013247
WBCnstr00037467
WBCnstr00043044
Construct_productWBCnstr00013247
WBCnstr00037467
WBCnstr00043044
Microarray_results (20)
Expression_cluster (84)
Interaction (14)
Map_infoMapVPosition3.6217Error0.001257
PositivePositive_cloneR07B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point (2)
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