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WormBase Tree Display for Gene: WBGene00004296

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Name Class

WBGene00004296EvidenceCGC_data_submission
SMapS_parentSequenceT04H1
IdentityVersion1
NameCGC_namerad-50
Sequence_nameT04H1.4
Molecular_nameT04H1.4a
T04H1.4a.1
CE21149
T04H1.4b
CE41010
T04H1.4b.1
Other_nameRAD50Accession_evidenceEMBLZ75312
CELE_T04H1.4Accession_evidenceNDBBX284605
Public_namerad-50
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:34WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrad
Allele (77)
StrainWBStrain00000283
WBStrain00000294
WBStrain00034801
WBStrain00034804
WBStrain00034810
RNASeq_FPKM (74)
GO_annotation (30)
Contained_in_operonCEOP5336
Ortholog (46)
Structured_descriptionConcise_descriptionrad-50 encodes the C. elegans ortholog of eukaryotic Rad50 and bacterial SbcC; RAD-50 is predicted to function, in a complex with MRE-11 and COM-1, in homology-mediated double-strand break (DSB) repair; genetic analyses indicate that rad-50 is required for a distinct pathway of meiotic DSB repair that functions from the onset of meiotic prophase through the midpachytene/late pachytene transition.Paper_evidenceWBPaper00031172
Curator_confirmedWBPerson1843
Date_last_updated13 Apr 2011 00:00:00
Automated_descriptionPredicted to enable G-quadruplex DNA binding activity; double-stranded telomeric DNA binding activity; and single-stranded telomeric DNA binding activity. Predicted to be involved in chromosome organization and nucleic acid metabolic process. Predicted to be located in condensed nuclear chromosome. Predicted to be part of Mre11 complex. Human ortholog(s) of this gene implicated in invasive ductal carcinoma and transitional cell carcinoma. Is an ortholog of human RAD50 (RAD50 double strand break repair protein).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:3008Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9816)
DOID:2671Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9816)
Molecular_infoCorresponding_CDST04H1.4a
T04H1.4b
Corresponding_transcriptT04H1.4a.1
T04H1.4b.1
Other_sequence (37)
Associated_featureWBsf647351
WBsf661875
WBsf1001543
WBsf1001544
WBsf1020546
Experimental_infoRNAi_result (12)
Expr_patternExpr1015956
Expr1032122
Expr1156042
Expr1200235
Expr1200237
Expr1200240
Expr2015240
Expr2033474
Drives_constructWBCnstr00035584
Construct_productWBCnstr00035584
Microarray_results (23)
Expression_cluster (165)
Interaction (185)
Map_infoMapVPosition3.91614Error0.007399
PositivePositive_cloneT04H1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5624
5284
5483
Pseudo_map_position
Reference (24)
RemarkSequence connection from [Boulton S, Vidal 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