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WormBase Tree Display for Gene: WBGene00006612

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Name Class

WBGene00006612SMapS_parentSequenceF45G2
IdentityVersion1
NameCGC_nametrf-1Person_evidenceWBPerson1122
Sequence_nameF45G2.6
Molecular_nameF45G2.6
F45G2.6.1
CE37519
Other_nameCELE_F45G2.6Accession_evidenceNDBBX284603
Public_nametrf-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtrf
Allele (58)
StrainWBStrain00029110
WBStrain00037405
RNASeq_FPKM (74)
GO_annotation (13)
Ortholog (48)
ParalogWBGene00022454Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionConcise_descriptiontrf-1 encodes the sole C. elegans ortholog of the Tumor Necrosis Factor (TNF) receptor-associated factor adaptor protein; from N- to C-terminus, TRF-1 has five domains: a RING finger domain, three cysteine-rich (CART) domains and a meprin-associated Traf homology (MATH) domain; trf-1(nr2014) mutant animals display a shortened lifespan and a diminished immune response to Salmonella enterica infection.Paper_evidenceWBPaper00004589
WBPaper00004692
WBPaper00031161
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated18 Jul 2014 00:00:00
Automated_descriptionPredicted to enable zinc ion binding activity. Involved in defense response to Gram-negative bacterium and innate immune response. Predicted to be located in cytoplasm. Expressed in CEMDL; CEMDR; CEMVL; CEMVR; and tail. Human ortholog(s) of this gene implicated in brain disease and lung adenocarcinoma. Is an ortholog of human TRAF4 (TNF receptor associated factor 4).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:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12034)
DOID:936Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12033)
Molecular_infoCorresponding_CDSF45G2.6
Corresponding_CDS_historyF45G2.6:wp132
Corresponding_transcriptF45G2.6.1
Associated_featureWBsf994891
WBsf226009
Experimental_infoRNAi_resultWBRNAi00095281Inferred_automaticallyRNAi_primary
WBRNAi00047439Inferred_automaticallyRNAi_primary
WBRNAi00032324Inferred_automaticallyRNAi_primary
WBRNAi00006284Inferred_automaticallyRNAi_primary
WBRNAi00076434Inferred_automaticallyRNAi_primary
WBRNAi00094757Inferred_automaticallyRNAi_primary
Expr_patternExpr14564
Expr16439
Expr1014051
Expr1151280
Expr2017493
Expr2035632
Drives_constructWBCnstr00034268
WBCnstr00041164
WBCnstr00043020
Construct_productWBCnstr00034268
Microarray_results (19)
Expression_cluster (58)
Interaction (58)
WBProcessWBbiopr:00000039
Map_infoMapIIIPosition21.2151Error0.000524
PositivePositive_cloneF45G2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4242
4739
Pseudo_map_position
Reference (19)
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