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WormBase Tree Display for Gene: WBGene00015658

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Name Class

WBGene00015658SMapS_parentSequenceC09G12
IdentityVersion2
NameCGC_nametsg-101Person_evidenceWBPerson3188
WBPerson1816
Sequence_nameC09G12.9
Molecular_nameC09G12.9
C09G12.9.1
CE34675
Other_nameCELE_C09G12.9Accession_evidenceNDBBX284604
Public_nametsg-101
DB_infoDatabaseAceViewgene4E276
WormQTLgeneWBGene00015658
WormFluxgeneWBGene00015658
NDBlocus_tagCELE_C09G12.9
PanthergeneCAEEL|WormBase=WBGene00015658|UniProtKB=O76258
familyPTHR23306
NCBIgene182474
RefSeqproteinNM_067963.6
TREEFAMTREEFAM_IDTF312917
TrEMBLUniProtAccO76258
UniProt_GCRPUniProtAccO76258
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
230 Oct 2007 14:27:24WBPerson2970Name_changeCGC_nametsg-101
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtsg
AlleleWBVar01514854
WBVar01514855
WBVar01514856
WBVar01668475
WBVar01630316
WBVar01922833
WBVar01922834
WBVar01630317
WBVar01922835
WBVar00602870
WBVar01630318
WBVar00249735
WBVar02008198
WBVar02096169
WBVar02094333
WBVar01990718
WBVar00275810
WBVar00275811
WBVar01274534
WBVar02156376
WBVar00187460
WBVar00187461
WBVar00187462
WBVar00187463
WBVar00187464
WBVar00187465
WBVar00187466
WBVar00187467
WBVar00187468
WBVar00187469
WBVar00187470
WBVar00187471
WBVar00187472
WBVar00187473
WBVar00187474
WBVar00187475
WBVar01965882
WBVar01965883
WBVar01965884
WBVar01965885
WBVar01965886
WBVar01965887
WBVar01965888
WBVar01821271
WBVar01965889
WBVar00421408
WBVar00421409
WBVar00421410
WBVar00421411
WBVar02073329
WBVar00421412
WBVar00421413
WBVar00421414
WBVar00421415
WBVar00421416
WBVar01499633
WBVar02077265
WBVar01997174
WBVar02020386
WBVar02020387
WBVar01910807
WBVar01910808
WBVar01727005
WBVar00571360
WBVar02036844
WBVar00899079
WBVar02003736
WBVar00899080
WBVar01500054
WBVar00899081
WBVar01500055
WBVar00899082
WBVar00899083
WBVar00899084
WBVar00899085
WBVar00899086
WBVar00899087
StrainWBStrain00002625
WBStrain00002534
WBStrain00051306
RNASeq_FPKM (74)
GO_annotation (13)
Contained_in_operonCEOP4088
Ortholog (46)
Structured_descriptionConcise_descriptiontsg-101 encodes the C. elegans ortholog of S. cerevisiae vacuolar protein sorting protein Vps23p and human TUMOR SUSCEPTIBILITY GENE 101 (TSG101; OMIM:601387), mutations in which are associated with several types of cancer and with varying responses to HIV infection; TSG-101 is an essential component of the C. elegans ESCRT-1 (Endosomal Sorting Complex Required for Transport, other members include VPS-28, VPS-37, and MVB-12) that is required for cell surface receptor degradation via the multivesicular body sorting pathway and hence, downregulation of receptor activity.Paper_evidenceWBPaper00026641
WBPaper00031035
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated09 Jul 2010 00:00:00
Automated_descriptionPredicted to enable ubiquitin binding activity. Involved in endosome to lysosome transport via multivesicular body sorting pathway and receptor catabolic process. Located in endosome membrane. Part of ESCRT I complex. Expressed in head and tail. Human ortholog(s) of this gene implicated in breast carcinoma and reproductive organ cancer (multiple). Is an ortholog of human TSG101 (tumor susceptibility 101).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:10283Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
DOID:2893Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
DOID:2870Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
DOID:3459Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
DOID:2394Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15971)
Molecular_infoCorresponding_CDSC09G12.9
Corresponding_CDS_historyC09G12.9:wp105
Corresponding_transcriptC09G12.9.1
Other_sequence (26)
Associated_featureWBsf667837
Experimental_infoRNAi_result (12)
Expr_patternChronogram751
Chronogram1424
Expr5223
Expr5224
Expr1020827
Expr1036705
Expr1144298
Expr2017537
Expr2035675
Drives_constructWBCnstr00003110
WBCnstr00004547
WBCnstr00028680
Construct_productWBCnstr00028680
Microarray_results (20)
Expression_cluster (76)
Interaction (45)
Map_infoMapIVPosition-3.31212Error0.00351
PositivePositive_cloneC09G12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
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