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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_name (4)
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
AlleleWBVar00427924
WBVar00427925
WBVar00427926
WBVar00427927
WBVar00427928
WBVar00427929
WBVar00427930
WBVar00190381
WBVar00919038
WBVar00919039
WBVar00919040
WBVar00919041
WBVar00919042
WBVar00919043
WBVar00919044
WBVar00919045
WBVar00919046
WBVar01499395
WBVar00919047
WBVar01499396
WBVar00919048
WBVar00919049
WBVar00919050
WBVar01823660
WBVar01491899
WBVar01794763
WBVar01499633
WBVar00249466
WBVar01668783
WBVar01500245
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