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WormBase Tree Display for Gene: WBGene00000545

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Name Class

WBGene00000545SMapS_parentSequenceY39A3CL
IdentityVersion1
NameCGC_nameclp-4Person_evidenceWBPerson349
Sequence_nameY39A3CL.5
Molecular_nameY39A3CL.5a
Y39A3CL.5a.1
CE33219
Other_nameCELE_Y39A3CL.5Accession_evidenceNDBBX284603
Public_nameclp-4
DB_infoDatabaseAceViewgene3C898
WormQTLgeneWBGene00000545
WormFluxgeneWBGene00000545
NDBlocus_tagCELE_Y39A3CL.5
PanthergeneCAEEL|WormBase=WBGene00000545|UniProtKB=Q8IAA9
familyPTHR10183
NCBIgene175326
RefSeqproteinNM_065059.10
TrEMBLUniProtAccQ8IAA9
UniProt_GCRPUniProtAccQ8IAA9
OMIMgene114220
114240
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classclp
Allele (292)
StrainWBStrain00032805
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (47)
Paralog (13)
Structured_descriptionConcise_descriptionclp-4 encodes a large calpain subunit that is homologous to Drosophila CalpainB and the mammalian muscle-specific Calpain 3 proteins (OMIM:114240, mutations are associated with limb-girdle muscular dystrophy); by homology, CLP-4 is predicted to function as a nonlysosomal, calcium-dependent, cysteine protease that is involved in intracellular proteolysis and peptidolysis; however, as loss of clp-4 activity via RNA-mediated interference (RNAi) does not result in any obvious abnormalities, the precise role of CLP-4 in C. elegans development and/or behavior is not yet known.Paper_evidenceWBPaper00004403
WBPaper00005654
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable calcium-dependent cysteine-type endopeptidase activity. Predicted to be involved in proteolysis. Predicted to be located in cytoplasm. Expressed in GABAergic neurons; body wall musculature; dorsal nerve cord; and ventral nerve cord. Human ortholog(s) of this gene implicated in Alzheimer's disease; autosomal dominant limb-girdle muscular dystrophy; autosomal recessive limb-girdle muscular dystrophy type 2A; hereditary spastic paraplegia 76; and stomach cancer. Is an ortholog of several human genes including CAPN1 (calpain 1); CAPN2 (calpain 2); and CAPN3 (calpain 3).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1476,HGNC:1479)
DOID:0110275Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1480)
DOID:0110273Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1480)
DOID:9884Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1480)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1486)
DOID:0110821Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1476)
Molecular_infoCorresponding_CDSY39A3CL.5a
Corresponding_CDS_historyY39A3CL.5b:wp282
Corresponding_transcriptY39A3CL.5a.1
Other_sequence (12)
Associated_feature (11)
Experimental_infoRNAi_result (15)
Expr_patternExpr10018
Expr1014965
Expr1030326
Expr1159658
Expr2010246
Expr2028488
Drives_constructWBCnstr00014643
Construct_productWBCnstr00014652
WBCnstr00014658
Microarray_results (22)
Expression_cluster (206)
Interaction (22)
Map_infoMapIIIPosition-16.0584Error0.022067
PositivePositive_cloneY39A3CLInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005513
WBPaper00025192
WBPaper00027531
WBPaper00038491
WBPaper00055090
WBPaper00065924
RemarkSequence connection from [Kuwabara PE]
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