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WormBase Tree Display for Gene: WBGene00006514

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Name Class

WBGene00006514SMapS_parentSequenceF44G4
IdentityVersion2
NameCGC_nametdp-1Person_evidenceWBPerson8505
Sequence_nameF44G4.4
Molecular_nameF44G4.4a
F44G4.4a.1
CE02231
F44G4.4c
CE44236
F44G4.4b
F44G4.4c.1
Other_nametag-169Person_evidenceWBPerson201
CELE_F44G4.4Accession_evidenceNDBBX284602
Public_nametdp-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
220 Nov 2008 11:55:56WBPerson2970Name_changeCGC_nametdp-1
Other_nametag-169
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtdp
Allele (24)
Possibly_affected_byWBVar02158431
WBVar02158432
WBVar02158433
WBVar02158434
WBVar02158435
WBVar02158436
WBVar02158437
StrainWBStrain00031640
WBStrain00035864
WBStrain00054779
RNASeq_FPKM (74)
GO_annotation (26)
Ortholog (38)
Paralog (12)
Structured_descriptionConcise_descriptiontdp-1 encodes the C. elegans ortholog of human TAR DNA/RNA binding protein TDP-43 (HGNC:TARDBP); in C. elegans TDP-1 is involved in the response to oxidative stress and age-dependent proteotoxicity; tdp-1 exhibits a dose-dependent effect on lifespan, and is required for the long lifespan and oxidative stress resistance of daf-2 mutants; based on homology to TDP-43, TDP-1 is predicted to have nucleic acid binding activity and function in RNA processing and metabolism; TDP-1 is widely expressed and in unstressed animals is found at low levels in the nucleus; in the presence of oxidative stress, however, TDP-1 levels increase.Paper_evidenceWBPaper00041295
Curator_confirmedWBPerson1843
WBPerson324
Date_last_updated31 Oct 2014 00:00:00
Automated_descriptionEnables chromatin binding activity and single-stranded RNA binding activity. Involved in several processes, including RNA splicing; determination of adult lifespan; and hyperosmotic response. Located in nucleus. Expressed in several structures, including body wall musculature; intestine; muscle cell; neurons; and pharynx. Used to study amyotrophic lateral sclerosis type 10. Human ortholog(s) of this gene implicated in Alzheimer's disease; Lewy body dementia; and progressive supranuclear palsy. Is an ortholog of human TARDBP (TAR DNA binding 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_infoExperimental_modelDOID:332Homo sapiensPaper_evidenceWBPaper00036365
Accession_evidenceOMIM612069
Curator_confirmedWBPerson324
Date_last_updated21 Feb 2013 00:00:00
DOID:0060201Homo sapiensPaper_evidenceWBPaper00064744
Curator_confirmedWBPerson324
Date_last_updated08 Jun 2023 00:00:00
Potential_modelDOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:0060201Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:14330Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:678Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:12217Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:231Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
DOID:11870Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11571)
Disease_relevanceHuman TAR DNA-binding protein, TDP43 (orthologous to elegans tdp-1), has been associated with several neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS) and frontotemporal lobar dementia (FTLD); ubiquinated inclusions of TDP43 have been found in the affected neurons of ALS, FTLD, as well as Alzheimer''s and Parkinson''s disease patients; modeling TDP43 proteinopathies in the worm employs two strategies: overexpressing mutant human TDP43 in transgenic worms and studying tdp-1, the elegans ortholog of human TDP43; overexpression of human ALS-linked mutant TDP43 in worms causes an uncoordianted phenotype and abnormal motor neuron synapses, characteristic of C. elegans mutants with motorneuron dysfunction; the overexpressed TDP43 localizes to the nucleus; the toxicity of human TDP43 is not due to interference with the endogenous elegans tdp-1/TDP43, as tdp-1 mutants have wild-type movement; human TDP43 toxicity in elegans requires nuclear accumulation of the full length protein and the presence of the TDP43 RNA recognition domains; TDP-43 neurotoxicity is independent of activity of the cell death caspase CED-3, further, phosphorylation of TDP-43 at serine residues drives mutant TDP-43 toxicity; studies with tdp-1, the ortholog of human TDP43 in elegans, indicate that tdp-1/TDP43 is a stress-responsive gene that functions in the Insulin/IGF pathway to regulate longevity, and is required for resistance to oxidative and osmotic stress; tdp-1 is also induced by the unfolded protein response (UPR) triggered by toxic proteins like mutant TDP43 itself, or ALS-linked mutated FUS, a nucleic acid binding protein related to TDP43.Homo sapiensPaper_evidenceWBPaper00036365
WBPaper00041295
WBPaper00040603
WBPaper00037845
Curator_confirmedWBPerson324
Date_last_updated30 Oct 2013 00:00:00
Models_disease_in_annotationWBDOannot00000300
Models_disease_assertedWBDOannot00001383
WBDOannot00001384
Molecular_infoCorresponding_CDSF44G4.4a
F44G4.4c
Corresponding_CDS_historyF44G4.4b:wp261
Corresponding_transcriptF44G4.4b
F44G4.4a.1
F44G4.4c.1
Other_sequence (23)
Associated_featureWBsf644524
WBsf644525
WBsf658043
WBsf658044
WBsf658045
WBsf988895
WBsf988896
WBsf1012783
Experimental_infoRNAi_resultWBRNAi00062253Inferred_automaticallyRNAi_primary
WBRNAi00014968Inferred_automaticallyRNAi_primary
WBRNAi00047340Inferred_automaticallyRNAi_primary
WBRNAi00032268Inferred_automaticallyRNAi_primary
WBRNAi00047341Inferred_automaticallyRNAi_primary
WBRNAi00092583Inferred_automaticallyRNAi_primary
Expr_patternExpr9483
Expr9920
Expr10097
Expr1016813
Expr1032669
Expr1151193
Expr2017368
Expr2035505
Drives_constructWBCnstr00009682
WBCnstr00014790
WBCnstr00037891
Construct_productWBCnstr00007042
WBCnstr00007043
WBCnstr00007044
WBCnstr00014048
WBCnstr00014790
WBCnstr00019743
WBCnstr00037891
Regulate_expr_clusterWBPaper00040603:tdp-1(lf)_down_vs_N2_FC_1.2
WBPaper00040603:tdp-1(lf)_down_vs_N2_FC_1.5
WBPaper00040603:tdp-1(lf)_up_vs_N2_FC_1.2
WBPaper00040603:tdp-1(lf)_up_vs_N2_FC_1.5
WBPaper00046012:tdp-1(ok803)_downregulated
WBPaper00046012:tdp-1(ok803)_upregulated
WBPaper00066004:tdp-1(csb38)_downregulated
WBPaper00066004:tdp-1(csb38)_upregulated
AntibodyWBAntibody00002583
WBAntibody00002820
Microarray_results (32)
Expression_cluster (100)
Interaction (53)
WBProcessWBbiopr:00000001
WBbiopr:00000046
WBbiopr:00000052
WBbiopr:00000061
WBbiopr:00000065
Map_infoMapIIPosition0.969489Error0.006139
PositivePositive_cloneF44G4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4858
4825
Pseudo_map_position
Reference (37)
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