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WormBase Tree Display for Gene: WBGene00006793

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Name Class

WBGene00006793EvidenceCGC_data_submission
SMapS_parentSequenceW09C5
IdentityVersion1
NameCGC_nameunc-59Person_evidenceWBPerson261
Sequence_nameW09C5.2
Molecular_nameW09C5.2
W09C5.2.1
CE20165
Other_nameunc-88
CELE_W09C5.2Accession_evidenceNDBBX284601
Public_nameunc-59
DB_infoDatabaseAceViewgene1O225
WormQTLgeneWBGene00006793
WormFluxgeneWBGene00006793
NDBlocus_tagCELE_W09C5.2
PanthergeneCAEEL|WormBase=WBGene00006793|UniProtKB=Q9U334
familyPTHR18884
NCBIgene173233
RefSeqproteinNM_060987.6
TrEMBLUniProtAccQ9U334
UniProt_GCRPUniProtAccQ9U334
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:43WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classunc
Reference_alleleWBVar00143070
AlleleWBVar00089479
WBVar00144021
WBVar02152777
WBVar01665141
WBVar01665142
WBVar00143677
WBVar02128927
WBVar00686401
WBVar01499739
WBVar00686402
WBVar00686403
WBVar00686404
WBVar00686405
WBVar00686406
WBVar00686407
WBVar00686408
WBVar02075496
WBVar00686409
WBVar00686410
WBVar00686411
WBVar00686412
WBVar00686413
WBVar00686414
WBVar00686415
WBVar00686416
WBVar00686417
WBVar00686418
WBVar00686419
WBVar00350715
WBVar00350716
WBVar00350717
WBVar00350718
WBVar00350719
WBVar00350720
WBVar00350721
WBVar00350722
WBVar00350723
WBVar00250889
WBVar00250900
WBVar00143070
WBVar01499998
WBVar01499999
WBVar01890759
WBVar00542247
WBVar01498939
WBVar01434532
WBVar00161040
WBVar00161041
WBVar00161042
WBVar00161043
WBVar00161044
WBVar00161045
Legacy_informatione261 : poor backward movement forward better; thin; vulva variably abnormal often protrusive sometimes ruptured; many postembryonic lineage abnormalities resulting from variable failures in cytokinesis; gonad lineages sometimes defective; males have very abnormal tail anatomy. ES2 ME0. NA2 (e1005 (pka unc-88)).
See unc-59.
See also e1005, e1465, n391
[C.elegansII] e261 : poor backward movement, forward better; thin; vulva variably abnormal, often protrusive, sometimes ruptured; many postembryonic lineage abnormalities resulting from variable failures in cytokinesis; gonad lineages sometimes defective; variable defects in neuroanatomy; males have very abnormal tail anatomy. ES2 ME0. OA3: e1005 (pka unc-88), e1465, n391. [Brenner 1974; White et al. 1982; MT]
StrainWBStrain00023968
WBStrain00027078
WBStrain00004226
WBStrain00004137
WBStrain00005472
WBStrain00008449
WBStrain00050769
RNASeq_FPKM (74)
GO_annotation (19)
Ortholog (54)
ParalogWBGene00015956Caenorhabditis elegansFrom_analysisPanther
WBGene00006795Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionunc-59, by alternative splicing, encodes two septin isoforms required (like the septins UNC-61A/B) for normal axonal migration, distal tip cell migration, and postembryonic cytokinesis (at the cellular level) and for normal locomotion and formation of the postembryonic vulva, somatic gonad, and male tail (at the organismal level); both UNC-59 and UNC-61A/B are dispensable for embryonic cytokinesis and development, but are thought to be required for all postembryonic cytokinesis; UNC-59 and UNC-61A/B depend on each other for localization to the cytokinetic furrow.Paper_evidenceWBPaper00000496
WBPaper00004453
WBPaper00006087
Curator_confirmedWBPerson567
Date_last_updated01 Feb 2006 00:00:00
Automated_descriptionPredicted to enable GTPase activity and molecular adaptor activity. Involved in egg-laying behavior; locomotion; and post-embryonic development. Located in cleavage furrow and midbody. Expressed in several structures, including buccal cavity; distal tip cell; germ line; pharynx; and sperm. Human ortholog(s) of this gene implicated in Lewy body dementia and Parkinson's disease. Is an ortholog of human SEPTIN7 (septin 7).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:12217Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9165)
DOID:14330Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9165)
Molecular_infoCorresponding_CDSW09C5.2
Corresponding_transcriptW09C5.2.1
Other_sequence (38)
Associated_feature (15)
Experimental_infoRNAi_result (38)
Expr_patternExpr2318
Expr2691
Expr3284
Expr14682
Expr1015124
Expr1032863
Expr1158568
Expr2017891
Expr2036027
Drives_constructWBCnstr00010902
Construct_productWBCnstr00005646
WBCnstr00010902
AntibodyWBAntibody00000329
WBAntibody00000930
Microarray_resultsSMD_0W09C5.2
SMD_W09C5.2
192287_at
A_12_P112088
Aff_W09C5.2
GPL13394_WBGene00006793
GPL13914_W09C5.2
GPL14144_W09C5.2_1073-1132_0.946_5_B
GPL14144_W09C5.2_1223-1282_0.966_1_A
GPL14144_W09C5.2_910-969_0.920_14_C
GPL19516_CGZ0038882
GPL21109_W09C5.2
GPL3518_CE20165
GPL8304_CE_WBGene00006793_A
GPL8304_CE_WBGene00006793_B
GPL8673_W09C5_2P00125
GPL8673_W09C5_2P00357
GPL8673_W09C5_2P00960
GPL9450_W09C5.2
cea2.p.19520
Expression_cluster (156)
Interaction (77)
Map_infoMapIPosition21.6174Error0.007359
Well_ordered
PositivePositive_cloneW09C5Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data2_point22
24
30
33
Multi_point (14)
Pos_neg_data (14)
Landmark_gene
Reference (49)
RemarkSequence connection from [Nguyen TQ, White JG]
MethodGene