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WormBase Tree Display for Gene: WBGene00004782

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Name Class

WBGene00004782SMapS_parentSequenceC26E6
IdentityVersion1
NameCGC_nameset-2Person_evidenceWBPerson632
Sequence_nameC26E6.9
Molecular_nameC26E6.9a
C26E6.9a.1
CE27735
C26E6.9b
CE01158
C26E6.9c
CE27736
C26E6.9b.1
C26E6.9c.1
Other_nameCELE_C26E6.9Accession_evidenceNDBBX284603
Public_nameset-2
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classset
Allele (92)
StrainWBStrain00027489
WBStrain00031733
WBStrain00032046
WBStrain00036215
WBStrain00000040
RNASeq_FPKM (74)
GO_annotation (21)
Contained_in_operonCEOP3240
Ortholog (40)
Paralog (19)
Structured_descriptionConcise_descriptionset-2 encodes a histone H3K4 methyltransferase closely related to the yeast Set1 and mammalian SET1/MLL proteins; SET-2 displays H3K4 methyltransferase activity in vitro and in C. elegans, regulates levels of H3K4; SET-2 plays a role in germline development, postembryonic development, negative regulation of lifespan in adult animals, and RNA interference; SET-2 localizes to nuclei.Paper_evidenceWBPaper00005020
WBPaper00032309
WBPaper00036383
Curator_confirmedWBPerson1843
Date_last_updated21 Sep 2010 00:00:00
Automated_descriptionEnables histone H3K4 methyltransferase activity. Involved in determination of adult lifespan and transdifferentiation. Located in nucleus. Expressed in several structures, including germ line; hermaphrodite distal tip cell; intestine; and nerve ring. Human ortholog(s) of this gene implicated in neurodevelopmental disorder with speech impairment and dysmorphic facies. Is an ortholog of human SETD1A (SET domain containing 1A, histone lysine methyltransferase).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:0070417Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29010)
DOID:0070471Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29010)
Molecular_infoCorresponding_CDSC26E6.9a
C26E6.9b
C26E6.9c
Corresponding_transcriptC26E6.9a.1
C26E6.9b.1
C26E6.9c.1
Other_sequence (35)
Associated_feature (11)
Experimental_infoRNAi_result (23)
Expr_pattern (14)
Drives_constructWBCnstr00005981
WBCnstr00013270
WBCnstr00013628
WBCnstr00019766
WBCnstr00020418
WBCnstr00035390
WBCnstr00042038
Construct_productWBCnstr00013270
WBCnstr00013628
WBCnstr00019766
WBCnstr00020473
WBCnstr00035390
Regulate_expr_cluster (12)
AntibodyWBAntibody00000438
Microarray_results (39)
Expression_cluster (151)
Interaction (45)
Map_infoMapIIIPosition-2.35202Error0.002862
PositivePositive_cloneC26E6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (65)
RemarkSequence connection from [Strome S], 02/06/13 krb.
Map 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