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WormBase Tree Display for Gene: WBGene00045237

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Name Class

WBGene00045237SMapS_parentSequenceF39H2
IdentityVersion2
NameCGC_namemrt-1Paper_evidenceWBPaper00035222
Person_evidenceWBPerson261
WBPerson7
Sequence_nameF39H2.5
Molecular_nameF39H2.5
F39H2.5.1
CE30531
Other_nameCELE_F39H2.5Accession_evidenceNDBBX284601
Public_namemrt-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 Jan 2007 14:53:24WBPerson480EventCreated
210 Nov 2009 16:03:51WBPerson1847EventAcquires_mergeWBGene00009564
Acquires_mergeWBGene00009564
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmrt
Allele (35)
StrainWBStrain00040705
WBStrain00040706
WBStrain00040709
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (42)
ParalogWBGene00007065Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
WBGene00010195Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionConcise_descriptionmrt-1 encodes a protein that contains an N-terminal domain homologous to the second OB DNA-binding fold of POT1 (Protection Of Telomeres 1)telomere-binding proteins and a C-terminal domain homologous to the SNM1 family nuclease domain; MRT-1 activity is required in vivo for regulation of telomere length and nucleotide excision repair (DNA crosslink repair); in vitro, MRT-1 exhibits 3'-5' exonuclease activity and single-stranded DNA-binding activity.Paper_evidenceWBPaper00035222
Curator_confirmedWBPerson1843
Date_last_updated28 Jan 2010 00:00:00
Automated_descriptionEnables 3'-5' exonuclease activity and single-stranded DNA binding activity. Involved in nucleotide-excision repair; reproduction; and telomere maintenance via telomerase. Predicted to be located in nucleus. Human ortholog(s) of this gene implicated in dyskeratosis congenita. Is an ortholog of human DCLRE1B (DNA cross-link repair 1B).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:2729Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17641)
Molecular_infoCorresponding_CDSF39H2.5
Corresponding_transcriptF39H2.5.1
Associated_featureWBsf643539
WBsf218191
Experimental_infoRNAi_resultWBRNAi00003642Inferred_automaticallyRNAi_primary
WBRNAi00007733Inferred_automaticallyRNAi_primary
WBRNAi00046806Inferred_automaticallyRNAi_primary
WBRNAi00077840Inferred_automaticallyRNAi_primary
Expr_patternExpr1025750
Expr1040351
Expr1150681
Expr2013761
Expr2031996
Drives_constructWBCnstr00023293
Construct_productWBCnstr00023293
AntibodyWBAntibody00001984
Microarray_results (19)
Expression_cluster (112)
InteractionWBInteraction000008924
WBInteraction000571757
WBInteraction000571761
Map_infoMapIPosition3.01633Error0.000295
PositivePositive_cloneF39H2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
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