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WormBase Tree Display for Gene: WBGene00015552

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Name Class

WBGene00015552SMapS_parentSequenceC06G3
IdentityVersion2
NameCGC_namegldi-4Person_evidenceWBPerson6609
WBPerson1816
Sequence_nameC06G3.6
Molecular_nameC06G3.6
C06G3.6.1
CE07982
C06G3.6.2
Other_nameCELE_C06G3.6Accession_evidenceNDBBX284604
Public_namegldi-4
DB_infoDatabaseAceViewgene4H783
WormQTLgeneWBGene00015552
WormFluxgeneWBGene00015552
NDBlocus_tagCELE_C06G3.6
PanthergeneCAEEL|WormBase=WBGene00015552|UniProtKB=Q17746
familyPTHR15090
NCBIgene177467
RefSeqproteinNM_068685.8
TrEMBLUniProtAccQ17746
UniProt_GCRPUniProtAccQ17746
OMIMgene601530
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
205 May 2023 12:43:53WBPerson51134Name_changeCGC_namegldi-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgldi
Allele (30)
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (19)
ParalogWBGene00011737Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012067Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012516Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021495Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable K63-linked polyubiquitin modification-dependent protein binding activity and protein kinase C binding activity. Predicted to be involved in aggrephagy; endosome organization; and mitophagy. Predicted to be located in aggresome and amphisome. Human ortholog(s) of this gene implicated in Paget's disease of bone 3; distal myopathy with rimmed vacuoles; and neurodegenerative disease (multiple). Is an ortholog of human SQSTM1 (sequestosome 1).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:0081366Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11280)
DOID:0110068Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11280)
DOID:0081363Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11280)
DOID:5408Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11280)
DOID:0081364Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11280)
Molecular_infoCorresponding_CDSC06G3.6
Corresponding_transcriptC06G3.6.1
C06G3.6.2
Other_sequencePPC14695_1
CRC07054_1
CR03421
Associated_featureWBsf646058
WBsf659792
Experimental_infoRNAi_resultWBRNAi00000578Inferred_automaticallyRNAi_primary
WBRNAi00028595Inferred_automaticallyRNAi_primary
WBRNAi00091188Inferred_automaticallyRNAi_primary
WBRNAi00010342Inferred_automaticallyRNAi_primary
WBRNAi00091189Inferred_automaticallyRNAi_primary
WBRNAi00090962Inferred_automaticallyRNAi_primary
WBRNAi00039938Inferred_automaticallyRNAi_primary
Expr_patternExpr1023085
Expr1036660
Expr1144012
Expr2000544
Expr2018770
Drives_constructWBCnstr00028757
Construct_productWBCnstr00028757
Microarray_results (17)
Expression_cluster (141)
Interaction (56)
Map_infoMapIVPosition3.27714
PositivePositive_cloneC06G3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
RemarkMap 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