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WormBase Tree Display for Gene: WBGene00004357

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Name Class

WBGene00004357SMapS_parentSequenceY51H4A
IdentityVersion1
NameCGC_namerho-1Person_evidenceWBPerson237
Sequence_nameY51H4A.3
Molecular_nameY51H4A.3a
Y51H4A.3a.1
CE25369
Y51H4A.3b
Other_nameRhoAAccession_evidenceEMBLL36965
Y51H4A.BPaper_evidenceWBPaper00004196
CELE_Y51H4A.3Accession_evidenceNDBBX284604
Public_namerho-1
DB_infoDatabaseAceViewgene4R428
WormQTLgeneWBGene00004357
WormFluxgeneWBGene00004357
NDBlocus_tagCELE_Y51H4A.3
PanthergeneCAEEL|WormBase=WBGene00004357|UniProtKB=Q22038
familyPTHR24072
NCBIgene178458
RefSeqproteinNR_131670.1
NM_070558.9
SwissProtUniProtAccQ22038
UniProt_GCRPUniProtAccQ22038
RNAcentralURSidURS00007B0C17
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrho
Allele (155)
StrainWBStrain00036907
WBStrain00047246
RNASeq_FPKM (74)
GO_annotation (40)
Ortholog (58)
ParalogWBGene00000390Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000424Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003239Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00004287Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012532Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022177Caenorhabditis elegansFrom_analysisPanther
WBGene00009059Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00019544Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionrho-1 encodes a Rho GTPase; rho-1 activity is required for regulation of a number of actin filament-based processes including embryonic polarity, cell migration, cell shape changes, muscle contraction, and neurite outgrowth; in addition, RHO-1 is required for both DGK-1- and UNC-13-dependent and independent regulation of synaptic signaling at neuromuscular junctions; as RHO-1 binds DGK-1 in vitro, its regulation of DGK-1-mediated signaling may be direct; in vitro RHO-1 GTPase activity is enhanced by the RGA-3 and RGA-4 GAP proteins, consistent with genetic studies showing that, in the early embryo, RHO-1 activity is required for expression of the rga-3/4(RNAi) hypercontractibility phenotype; RHO-1 is ubiquitously expressed throughout development with notably high expression seen in head neurons and asymmetric expression seen in the anterior cortex of one-cell embryos.Paper_evidenceWBPaper00002066
WBPaper00004340
WBPaper00004959
WBPaper00013415
WBPaper00027016
WBPaper00028358
WBPaper00028408
WBPaper00031005
Curator_confirmedWBPerson1843
Date_last_updated13 Sep 2007 00:00:00
Automated_descriptionEnables several functions, including GTP binding activity; GTPase activating protein binding activity; and GTPase activity. Involved in several processes, including actomyosin structure organization; positive regulation of acetylcholine secretion, neurotransmission; and positive regulation of locomotion. Located in cell cortex and cleavage furrow. Expressed widely. Human ortholog(s) of this gene implicated in several diseases, including colorectal cancer; multiple sclerosis; and ovarian carcinoma. Is an ortholog of human RHOA (ras homolog family member A).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:9256Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667)
DOID:11054Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667)
DOID:2377Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667)
DOID:3459Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667)
DOID:4001Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667,HGNC:669)
DOID:1612Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:667,HGNC:668,HGNC:669)
Molecular_infoCorresponding_CDSY51H4A.3a
Corresponding_transcriptY51H4A.3b
Y51H4A.3a.1
Other_sequence (67)
Associated_feature (14)
Experimental_infoRNAi_result (53)
Expr_pattern (11)
Construct_product (11)
AntibodyWBAntibody00000091
WBAntibody00001137
Microarray_results (18)
Expression_cluster (119)
Interaction (279)
Map_infoMapIVPosition15.09Error0.001168
PositivePositive_cloneY51H4AInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004196
WBPaper00004340
WBPaper00004959
WBPaper00010073
WBPaper00011658
WBPaper00012556
WBPaper00013415
WBPaper00017093
WBPaper00018840
WBPaper00019316
WBPaper00023327
WBPaper00023414
WBPaper00025137
WBPaper00026732
WBPaper00026774
WBPaper00026850
WBPaper00026937
WBPaper00027016
WBPaper00027071
WBPaper00027197
WBPaper00027235
WBPaper00027296
WBPaper00027345
WBPaper00027672
WBPaper00027923
WBPaper00027954
WBPaper00028001
WBPaper00028358
WBPaper00028395
WBPaper00028408
WBPaper00028856
WBPaper00030733
WBPaper00030892
WBPaper00031005
WBPaper00031968
WBPaper00032195
WBPaper00032405
WBPaper00032779
WBPaper00033015
WBPaper00033521
WBPaper00034079
WBPaper00034638
WBPaper00035488
WBPaper00036989
WBPaper00037522
WBPaper00037607
WBPaper00037900
WBPaper00038084
WBPaper00038091
WBPaper00038212
WBPaper00038491
WBPaper00038635
WBPaper00038646
WBPaper00038649
WBPaper00038650
WBPaper00038668
WBPaper00038843
WBPaper00039146
WBPaper00039240
WBPaper00039254
WBPaper00040835
WBPaper00041129
WBPaper00041637
WBPaper00041771
WBPaper00041891
WBPaper00042325
WBPaper00042732
WBPaper00042733
WBPaper00042771
WBPaper00043301
WBPaper00043387
WBPaper00043426
WBPaper00043453
WBPaper00044157
WBPaper00044595
WBPaper00045955
WBPaper00046168
WBPaper00046208
WBPaper00046221
WBPaper00046313
WBPaper00046675
WBPaper00047112
WBPaper00047484
WBPaper00048213
WBPaper00048291
WBPaper00048842
WBPaper00049131
WBPaper00049309
WBPaper00049828
WBPaper00050540
WBPaper00050656
WBPaper00051821
WBPaper00052274
WBPaper00052765
WBPaper00053276
WBPaper00054438
WBPaper00055035
WBPaper00055090
WBPaper00055279
WBPaper00055350
WBPaper00055566
WBPaper00056137
WBPaper00056801
WBPaper00056927
WBPaper00057747
WBPaper00057748
WBPaper00058265
WBPaper00059624
WBPaper00060754
WBPaper00060897
WBPaper00061150
WBPaper00061290
WBPaper00061388
WBPaper00061553
WBPaper00061837
WBPaper00062045
WBPaper00062488
WBPaper00062625
WBPaper00063057
WBPaper00064064
WBPaper00064561
WBPaper00064780
WBPaper00064804
WBPaper00064936
WBPaper00065275
WBPaper00066087
RemarkSequence connection from [Spencer AG, Han M]
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