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WormBase Tree Display for Gene: WBGene00003040

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Name Class

WBGene00003040SMapS_parentSequenceT12F5
IdentityVersion1
NameCGC_namelin-59Person_evidenceWBPerson261
Sequence_nameT12F5.4
Molecular_nameT12F5.4
T12F5.4.1
CE13601
Other_nameCELE_T12F5.4Accession_evidenceNDBBX284601
Public_namelin-59
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlin
AlleleWBVar00627984
WBVar00070764
WBVar00627985
WBVar00627986
WBVar00627987
WBVar01640791
WBVar01640792
WBVar00627988
WBVar00627989
WBVar00627990
WBVar00627991
WBVar00627992
WBVar00627993
WBVar00627994
WBVar00627995
WBVar00627996
WBVar01545942
WBVar01496061
WBVar01846277
WBVar00331014
WBVar00331015
WBVar00331016
WBVar00331017
WBVar00331018
WBVar01431176
WBVar00331019
WBVar01431177
WBVar00331020
WBVar01431178
WBVar00331021
WBVar00331022
WBVar00331023
WBVar00031011
WBVar00331024
WBVar00331025
WBVar00331026
WBVar00331027
WBVar00251061
WBVar00331028
WBVar00331029
WBVar02039414
WBVar00331030
WBVar00331031
WBVar00242580
WBVar00331032
WBVar01398884
WBVar00094835
WBVar01499786
WBVar01499985
WBVar01411417
WBVar01411418
WBVar00278504
WBVar00278505
WBVar02055531
WBVar01488586
WBVar01556382
WBVar02126977
WBVar02126978
WBVar00304909
WBVar00627949
WBVar00627950
WBVar00627951
WBVar00627952
WBVar00627953
WBVar00152584
WBVar01280854
WBVar00627954
WBVar01280855
WBVar00627955
WBVar00627956
WBVar01280856
WBVar01280857
WBVar00627957
WBVar01280858
WBVar00627958
WBVar00627959
WBVar01280859
WBVar01280860
WBVar00627960
WBVar00627961
WBVar01280861
WBVar00627962
WBVar01280863
WBVar00627963
WBVar00627964
WBVar01280864
WBVar01280865
WBVar00627965
WBVar00627966
WBVar01280866
WBVar00627967
WBVar01280867
WBVar01280868
WBVar00627968
WBVar01280869
WBVar00627969
WBVar00627970
WBVar00627971
WBVar00627972
WBVar00627973
WBVar00627974
WBVar00627975
WBVar00627976
WBVar00627977
WBVar00627978
WBVar00627979
WBVar00627980
WBVar00627981
WBVar00627982
WBVar00627983
Legacy_information[Chamberlin HM] sa489 males have abnormal tail development, with altered F and U cell lineages. F and U also abnormal in hermaphrodite.
StrainWBStrain00022835
WBStrain00029537
WBStrain00005831
RNASeq_FPKM (74)
GO_annotation (26)
Ortholog (40)
Paralog (19)
Structured_descriptionConcise_descriptionlin-59 encodes a SET domain-containing protein that is most closely related to the ASH1 group of histone-lysine N-methyltransferases; lin-59 was originally identified in screens for mutations that disrupt male tail development and subsequently was shown to be an essential gene required for development and fate specification of a number of different cells types, including those of the male tail, male and hermaphrodite hindgut, and egg-laying system; lin-59 has been shown to positively regulate expression of at least four genes: cdh-3, egl-5, mab-5, and nac-2; a lin-59::gfp reporter fusion is first expressed during the proliferative stage of embryonic development and expression continues, in most cells, throughout larval development and adulthood.Paper_evidenceWBPaper00003719
WBPaper00003938
Curator_confirmedWBPerson1843
Date_last_updated27 Mar 2008 00:00:00
Automated_descriptionPredicted to enable histone H3K36 methyltransferase activity. Involved in several processes, including ectodermal cell fate specification; egg-laying behavior; and nematode male tail tip morphogenesis. Predicted to be located in nucleus. Predicted to be part of chromatin. Expressed in hypodermis; intestine; and muscle cell. Used to study leukemia. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 52. Is an ortholog of human ASH1L (ASH1 like 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_infoExperimental_modelDOID:1240Homo sapiensPaper_evidenceWBPaper00032952
Curator_confirmedWBPerson38202
Date_last_updated13 Jun 2018 00:00:00
Potential_modelDOID:0080231Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19088)
Models_disease_assertedWBDOannot00000546
Molecular_infoCorresponding_CDST12F5.4
Corresponding_transcriptT12F5.4.1
Other_sequence (20)
Associated_feature (15)
Transcription_factorWBTranscriptionFactor000311
Experimental_infoRNAi_result (19)
Expr_patternExpr658
Expr14359
Expr1025648
Expr1031425
Expr1156808
Expr2013195
Expr2031427
Drives_constructWBCnstr00012479
WBCnstr00036267
Construct_productWBCnstr00036267
Microarray_results (18)
Expression_cluster (131)
Interaction (126)
Map_infoMapIPosition-2.83104Error0.022529
Well_ordered
PositiveInside_rearrqDf3
Positive_cloneT12F5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point3669
3670
3671
3672
3782
4354
4429
Pos_neg_data10214
Reference (22)
MethodGene