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WormBase Tree Display for Gene: WBGene00011737

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Name Class

WBGene00011737SMapS_parentSequenceT12G3
IdentityVersion2
NameCGC_namesqst-1Paper_evidenceWBPaper00042170
Person_evidenceWBPerson716
Sequence_nameT12G3.1
Molecular_nameT12G3.1a
T12G3.1a.1
CE37554
T12G3.1b
CE45860
T12G3.1b.1
Other_nameCELE_T12G3.1Accession_evidenceNDBBX284604
Public_namesqst-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:52WBPerson1971EventImportedInitial conversion from CDS class of WS125
205 Apr 2013 16:46:51WBPerson2970Name_changeCGC_namesqst-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsqst
Allele (53)
StrainWBStrain00001490
WBStrain00037114
WBStrain00037157
Component_of_genotypeWBGenotype00000083
WBGenotype00000084
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (32)
ParalogWBGene00012067Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012516Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015552Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021495Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionsqst-1 encodes a protein with similarity to mammalian sequestosome 1(SQSTM1)/p62, a signal transduction or adaptor protein involved in receptor-mediated signalling pathways; SQST-1 is weakly expressed in embryos and exhibits a diffuse, cytoplasmic localization; SQST-1 is selectively removed by autophagy during embryogenesis.Paper_evidenceWBPaper00036384
WBPaper00041409
Curator_confirmedWBPerson1843
Date_last_updated12 Oct 2012 00:00:00
Automated_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. Located in cytoplasm. Expressed in several structures, including head; hypodermal cell; muscle cell; tail; and vulva. 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_infoExperimental_modelDOID:332Homo sapiensPaper_evidenceWBPaper00066343
Curator_confirmedWBPerson324
Date_last_updated31 Aug 2021 00:00:00
Potential_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)
Models_disease_assertedWBDOannot00001040
Molecular_infoCorresponding_CDST12G3.1a
T12G3.1b
Corresponding_CDS_historyT12G3.1:wp132
Corresponding_transcriptT12G3.1a.1
T12G3.1b.1
Other_sequenceCBC08481_1
CR00634
CRC06360_1
CBC06086_1
CR03354
CBC12582_1
CR01694
CJC06184_1
CRC08734_1
CRC12404_1
Associated_featureWBsf646442
WBsf660776
WBsf660777
WBsf660778
WBsf981832
WBsf998015
WBsf1018314
WBsf229233
WBsf229234
WBsf229235
Experimental_infoRNAi_resultWBRNAi00113609Inferred_automaticallyRNAi_primary
WBRNAi00114688Inferred_automaticallyRNAi_primary
WBRNAi00033299Inferred_automaticallyRNAi_primary
WBRNAi00018644Inferred_automaticallyRNAi_primary
WBRNAi00053225Inferred_automaticallyRNAi_primary
Expr_pattern (19)
Drives_constructWBCnstr00002349
WBCnstr00004318
WBCnstr00006906
WBCnstr00014783
WBCnstr00030429
Construct_productWBCnstr00006906
WBCnstr00019922
WBCnstr00030429
AntibodyWBAntibody00002145
WBAntibody00002774
WBAntibody00002865
WBAntibody00002887
Microarray_results (23)
Expression_cluster (335)
Interaction (77)
Map_infoMapIVPosition5.51952
PositivePositive_cloneT12G3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00026285
WBPaper00034348
WBPaper00036384
WBPaper00040314
WBPaper00041409
WBPaper00042170
WBPaper00042320
WBPaper00044390
WBPaper00045184
WBPaper00046305
WBPaper00046758
WBPaper00049063
WBPaper00051658
WBPaper00052899
WBPaper00054228
WBPaper00054669
WBPaper00054980
WBPaper00055267
WBPaper00056693
WBPaper00056905
WBPaper00057472
WBPaper00058118
WBPaper00060613
WBPaper00060923
WBPaper00061178
WBPaper00061251
WBPaper00061739
WBPaper00061951
WBPaper00062277
WBPaper00062407
WBPaper00062653
WBPaper00064006
WBPaper00064683
WBPaper00065267
WBPaper00065749
WBPaper00066086
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