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WormBase Tree Display for Gene: WBGene00016603

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Name Class

WBGene00016603SMapS_parentSequenceC43E11
IdentityVersion2
NameCGC_namemet-1Person_evidenceWBPerson1730
WBPerson268
Sequence_nameC43E11.3
Molecular_nameC43E11.3a
C43E11.3a.1
CE30503
C43E11.3b
CE08681
C43E11.3b.1
C43E11.3b.2
C43E11.3b.3
Other_nameCELE_C43E11.3Accession_evidenceNDBBX284601
Public_namemet-1
DB_infoDatabaseWormQTLgeneWBGene00016603
WormFluxgeneWBGene00016603
NDBlocus_tagCELE_C43E11.3
PanthergeneCAEEL|WormBase=WBGene00016603|UniProtKB=A4LBC2
familyPTHR22884
NCBIgene172026
RefSeqproteinNM_058939.6
NM_182042.4
TREEFAMTREEFAM_IDTF352219
TrEMBLUniProtAccA4LBC3
A4LBC2
UniProt_GCRPUniProtAccA4LBC2
OMIMgene612778
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
223 Mar 2007 15:51:10WBPerson1849EventAcquires_mergeWBGene00044017
Acquires_mergeWBGene00044017
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmet
Allele (162)
StrainWBStrain00036305
WBStrain00027452
WBStrain00027568
WBStrain00036778
RNASeq_FPKM (74)
GO_annotation (19)
Contained_in_operonCEOP1168
Ortholog (100)
Paralog (19)
Structured_descriptionConcise_descriptionmet-1 encodes a histone methyltransferase whose SET domain is similar to that of Saccharomyces cerevisiae Set2p; loss of met-1 activity in the background of a mutant class A synMuv gene, such as lin-15A, results in a multivulval phenotype, indicating that met-1 acts to negatively regulate vulval cell fate specification; as met-1 is required for normal levels of histone H3K36 and H3K9 trimethylation and met-1;lin-15A animals show an increase in lin-3 EGF expression, met-1 likely acts as part of a transcriptional repressor complex that negatively regulates lin-3 EGF transcription to restrict vulval development to three of the six cells in the vulval equivalence group; in addition, genetic studies indicate that met-1 likely acts redundantly with met-2 to inhibit vulval cell fates.Paper_evidenceWBPaper00030864
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated01 Apr 2008 00:00:00
Automated_descriptionEnables histone H3K36 methyltransferase activity. Involved in negative regulation of transcription by RNA polymerase II and negative regulation of vulval development. Predicted to be located in nucleus. Predicted to be part of chromatin. Expressed in hypodermis; intestine; and muscle cell. Human ortholog(s) of this gene implicated in several diseases, including carcinoma (multiple); gastrointestinal system cancer (multiple); and idiopathic pulmonary fibrosis. Is an ortholog of human SETD2 (SET domain containing 2, 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:0060307Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:9256Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:4467Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:9253Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:0050156Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:3910Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:7474Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:3571Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
DOID:1790Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18420)
Molecular_infoCorresponding_CDSC43E11.3a
C43E11.3b
Corresponding_CDS_historyC43E11.3:wp173
C43E11.3a:wp136
C43E11.3b:wp90
C43E11.3b:wp136
Corresponding_transcriptC43E11.3a.1
C43E11.3b.1
C43E11.3b.2
C43E11.3b.3
Other_sequenceCR05423
MH05940
CRC07104_1
CRC07781_1
Associated_feature (14)
Experimental_infoRNAi_result (12)
Expr_patternExpr14350
Expr1016667
Expr1037129
Expr1146371
Expr2013535
Expr2031769
Drives_constructWBCnstr00027945
Construct_productWBCnstr00027945
Regulate_expr_clusterWBPaper00064315:met-1(bn200)_downregulated_PGCs
WBPaper00064315:met-1(bn200)_upregulated_PGCs
AntibodyWBAntibody00002850
Microarray_results (28)
Expression_cluster (131)
Interaction (39)
Map_infoMapIPosition-1.53098Error0.003143
PositivePositive_cloneC43E11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5329
4507
Pseudo_map_position
Reference (30)
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