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WormBase Tree Display for Gene: WBGene00004382

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Name Class

WBGene00004382SMapS_parentSequenceF59A6
IdentityVersion3
NameCGC_namernh-1.0Paper_evidenceWBPaper00027023
Sequence_nameF59A6.6
Molecular_name (11)
Other_namernh-1Paper_evidenceWBPaper00005577
CELE_F59A6.6Accession_evidenceNDBBX284602
Public_namernh-1.0
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
224 Mar 2006 09:56:26WBPerson2970Name_changeCGC_namernh-1.0
Other_namernh-1
306 Apr 2006 09:52:55WBPerson2970EventAcquires_mergeWBGene00019088
Acquires_mergeWBGene00019088
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrnh
Allele (41)
RNASeq_FPKM (74)
GO_annotation (16)
Contained_in_operonCEOP2727
CEOP2152
Ortholog (36)
ParalogWBGene00010787Caenorhabditis elegansFrom_analysisTreeFam
Panther
WBGene00011664Caenorhabditis elegansFrom_analysisPanther
WBGene00007303Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00022888Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionrnh-1.0 is one of four C. elegans genes that can encode an RNase H ribonuclease; when expressed in vitro, RNH-1.0 isoforms exhibit RNase H activity; rnh-1.0 transcripts are expressed throughout development.Paper_evidenceWBPaper00005577
WBPaper00004424
WBPaper00027023
Curator_confirmedWBPerson1843
WBPerson1983
Date_last_updated25 Feb 2014 00:00:00
Automated_descriptionEnables RNA-DNA hybrid ribonuclease activity. Predicted to be involved in DNA replication, removal of RNA primer. Human ortholog(s) of this gene implicated in autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 2. Is an ortholog of human RNASEH1 (ribonuclease H1).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:0111515Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18466)
Molecular_infoCorresponding_CDSF59A6.6a
F59A6.6b
F59A6.6c
Corresponding_CDS_historyF59A6.6a:wp97
F59A6.6d:wp242
F59A6.6d:wp260
Corresponding_transcriptF59A6.6a.1
F59A6.6a.2
F59A6.6a.3
F59A6.6b.1
F59A6.6c.1
Other_sequence (65)
Associated_featureWBsf657563
WBsf221212
WBsf221213
WBsf221214
Experimental_infoRNAi_resultWBRNAi00025766Inferred_automaticallyRNAi_primary
WBRNAi00016054Inferred_automaticallyRNAi_primary
WBRNAi00049116Inferred_automaticallyRNAi_primary
WBRNAi00078467Inferred_automaticallyRNAi_primary
WBRNAi00016055Inferred_automaticallyRNAi_primary
WBRNAi00000333Inferred_automaticallyRNAi_primary
WBRNAi00027380Inferred_automaticallyRNAi_primary
Expr_patternExpr3820
Expr3821
Expr3822
Expr3823
Expr3824
Expr1028224
Expr1032193
Expr1152860
Expr2015385
Expr2033619
Drives_constructWBCnstr00035523
Construct_productWBCnstr00035523
Microarray_results (48)
Expression_cluster (104)
InteractionWBInteraction000123851
WBInteraction000134092
WBInteraction000138973
WBInteraction000576717
Map_infoMapIIPosition-2.60048Error0.00164
PositivePositive_cloneF59A6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005577
WBPaper00027023
WBPaper00038491
WBPaper00055090
WBPaper00064312
WBPaper00065080
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