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WormBase Tree Display for Gene: WBGene00017482

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Name Class

WBGene00017482SMapS_parentSequenceF15E6
IdentityVersion2
NameCGC_nameset-9Person_evidenceWBPerson1730
WBPerson268
WBPerson632
Sequence_nameF15E6.1
Molecular_nameF15E6.1
F15E6.1.1
CE48653
Other_nameCELE_F15E6.1Accession_evidenceNDBBX284604
Public_nameset-9
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
203 May 2007 10:33:07WBPerson2970Name_changeCGC_nameset-9
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classset
Allele (179)
StrainWBStrain00027554
RNASeq_FPKM (74)
GO_annotation00032541
00032542
00032543
00032544
00032545
00032546
00032547
00032548
00032549
00032550
Ortholog (29)
ParalogWBGene00013106Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00022203Caenorhabditis elegansFrom_analysisTreeFam
Panther
WBGene00012845Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionset-9 encodes a large (1,655-residue) protein with a low-complexity N-terminal region, followed by a PHD-zinc finger and a SET domain; SET-9 has no non-nematode orthologs, but has 96% identity (1616/1679 residues) to its paralog SET-26; SET-9 is required for a normally short lifespan and low spontaneous mutation rate; life extension by set-9(RNAi) requires DAF-16, indicating that SET-9 limits normal lifespan by negatively regulating DAF-16 (either directly or indirectly); otherwise, neither set-9(n4949) nor set-9(RNAi) have any obvious phenotypes.Paper_evidenceWBPaper00005736
WBPaper00026643
WBPaper00030864
Curator_confirmedWBPerson567
Date_last_updated11 Oct 2007 00:00:00
Automated_descriptionPredicted to enable histone methyltransferase activity and metal ion binding activity. Involved in determination of adult lifespan. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in several diseases, including autosomal dominant intellectual developmental disorder 23; esophagus squamous cell carcinoma; and prostate cancer. Is an ortholog of human SETD5 (SET domain containing 5).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:3748Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25566)
DOID:10283Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25566)
DOID:0070053Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25566)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:25566)
Molecular_infoCorresponding_CDSF15E6.1
Corresponding_CDS_historyF15E6.1:wp239
Corresponding_transcriptF15E6.1.1
Other_sequence (12)
Associated_featureWBsf660093
WBsf981738
WBsf228184
Transcription_factorWBTranscriptionFactor000774
Experimental_infoRNAi_result (29)
Expr_patternExpr9865
Expr14392
Expr14393
Expr1019881
Expr1037519
Expr1148706
Expr2015783
Expr2034016
Regulate_expr_clusterWBPaper00054410:set-9(rw5)_downregulated
WBPaper00054410:set-9(rw5)_upregulated
Microarray_results (19)
Expression_cluster (149)
Interaction (17)
Map_infoMapIVPosition0.147586
PositivePositive_cloneF15E6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (14)
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