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WormBase Tree Display for Gene: WBGene00001983

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Name Class

WBGene00001983EvidencePerson_evidenceWBPerson367
SMapS_parentSequenceE04A4
IdentityVersion1
NameCGC_namehoe-1Person_evidenceWBPerson367
Sequence_nameE04A4.4
Molecular_nameE04A4.4a
E04A4.4a.1
CE29748
E04A4.4b
CE36588
E04A4.4c
CE48594
E04A4.4b.1
E04A4.4c.1
Other_nameCELE_E04A4.4Accession_evidenceNDBBX284604
Public_namehoe-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhoe
Allele (51)
StrainWBStrain00049335
RNASeq_FPKM (74)
GO_annotation (19)
Contained_in_operonCEOP4144
Ortholog (38)
Structured_descriptionConcise_descriptionhoe-1 encodes, by alternative splicing, two isoforms of a putative metal-dependent hydrolase orthologous to human ELAC2; HOE-1 is required for fertility, normal growth progression during the late larval stages and germ line proliferation; since hoe-1(RNAi) animals do not produce gametes, hoe-1 may be required for mitosis and meiosis; hoe-1 deficiency suppresses the multivulva (Muv) phenotype of activated LET-60/RAS, while having no effect on other RAS pathway members.Paper_evidenceWBPaper00005654
WBPaper00006401
Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated29 Aug 2007 00:00:00
Automated_descriptionPredicted to enable 3'-tRNA processing endoribonuclease activity. Involved in nematode larval development; positive regulation of vulval development; and sexual reproduction. Predicted to be located in mitochondrion. Expressed in germ line. Used to study prostate cancer. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 17. Is an ortholog of human ELAC2 (elaC ribonuclease Z 2).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:10283Homo sapiensPaper_evidenceWBPaper00006401
Accession_evidenceOMIM614731
Curator_confirmedWBPerson324
Date_last_updated24 Oct 2013 00:00:00
Potential_modelDOID:0111496Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14198)
Disease_relevanceThe human ELAC2/HPC2 gene is a prostate cancer susceptibility gene and encodes a gene product containing a well-conserved histidine motif domain found in metal dependent hydrolases; ELAC2 has tRNA endonuclease activity and is highly expressed in the testis; in C. elegans, reduction of function of the orthologous hoe-1, results in slow-growing, sterile animals that cannot produce gametes; hoe-1 is required for germ cells to progress through mitosis and loss of hoe-1 results in severely under-proliferated germ lines, consistent with a role of regulating cell proliferation in humans; further hoe-1 knockdown suppresses let-60/Ras activating mutations in elegans.Homo sapiensPaper_evidenceWBPaper00006401
Accession_evidenceOMIM614731
605367
Curator_confirmedWBPerson324
Date_last_updated02 May 2014 00:00:00
Modifies_diseaseDOID:10283
Models_disease_in_annotationWBDOannot00000240
Modifies_disease_in_annotationWBDOannot00000788
Molecular_infoCorresponding_CDSE04A4.4a
E04A4.4b
E04A4.4c
Corresponding_transcriptE04A4.4a.1
E04A4.4b.1
E04A4.4c.1
Other_sequence (48)
Associated_featureWBsf667903
WBsf996385
WBsf230003
WBsf230004
Experimental_infoRNAi_result (32)
Expr_patternExpr2875
Expr1026531
Expr1031152
Expr1147648
Expr2012534
Expr2030773
Drives_constructWBCnstr00036542
Construct_productWBCnstr00036542
Microarray_results (24)
Expression_cluster (147)
Interaction (164)
Map_infoMapIVPosition0.747216Error0.009606
PositivePositive_cloneE04A4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00006401
WBPaper00035429
WBPaper00038491
WBPaper00055090
WBPaper00063922
WBPaper00063971
WBPaper00065026
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