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WormBase Tree Display for Gene: WBGene00001093

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Name Class

WBGene00001093SMapS_parentSequenceT12E12
IdentityVersion1
NameCGC_namedrp-1Person_evidenceWBPerson733
Sequence_nameT12E12.4
Molecular_nameT12E12.4a
T12E12.4a.1
CE30172
T12E12.4b
CE30173
T12E12.4a.2
T12E12.4b.1
T12E12.4b.2
Other_nameCELE_T12E12.4Accession_evidenceNDBBX284604
Public_namedrp-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdrp
Allele (45)
StrainWBStrain00005196
WBStrain00007389
WBStrain00007408
WBStrain00007414
RNASeq_FPKM (74)
GO_annotation (30)
Contained_in_operonCEOP4168
Ortholog (39)
ParalogWBGene00001134Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001130Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptiondrp-1 encodes a dynamin-related protein, orthologous to Dnm1p in S. cerevisiae and DRP1 in mammals, that is required for severing of the mitochondrial outer membrane during mitochondrial division.Paper_evidenceWBPaper00003790
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable GTP binding activity; GTPase activity; and microtubule binding activity. Involved in apoptotic mitochondrial changes; embryo development; and mitochondrial fission. Located in mitochondrion. Expressed in several structures, including germ line; non-striated muscle; preanal ganglion; rectal muscle; and somatic nervous system. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in Alzheimer's disease; encephalopathy due to defective mitochondrial and peroxisomal fission 1; optic atrophy 5; and pulmonary fibrosis. Is an ortholog of human DNM1L (dynamin 1 like).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:14330Homo sapiensPaper_evidenceWBPaper00057005
Curator_confirmedWBPerson324
Date_last_updated20 Feb 2020 00:00:00
Potential_modelDOID:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2973)
DOID:0070347Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2973)
DOID:0111438Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2973)
DOID:3770Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2973)
Models_disease_assertedWBDOannot00000741
Molecular_infoCorresponding_CDST12E12.4a
T12E12.4b
Corresponding_transcriptT12E12.4a.1
T12E12.4a.2
T12E12.4b.1
T12E12.4b.2
Other_sequence (72)
Associated_featureWBsf655022
WBsf660150
WBsf981759
WBsf996535
WBsf228316
WBsf228317
WBsf228318
Experimental_infoRNAi_result (36)
Expr_patternExpr543
Expr11473
Expr12437
Expr1017306
Expr1030697
Expr1156803
Expr2011094
Expr2029330
Drives_constructWBCnstr00012431
WBCnstr00037085
Construct_productWBCnstr00005418
WBCnstr00005420
WBCnstr00009299
WBCnstr00012431
WBCnstr00019040
WBCnstr00037085
AntibodyWBAntibody00001689
Microarray_results (33)
Expression_cluster (152)
Interaction (114)
Map_infoMapIVPosition1.82105Error0.005501
PositivePositive_cloneT12E12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00003790
WBPaper00004211
WBPaper00005928
WBPaper00017000
WBPaper00017049
WBPaper00017548
WBPaper00017869
WBPaper00018470
WBPaper00018471
WBPaper00023353
WBPaper00024031
WBPaper00024200
WBPaper00027283
WBPaper00027647
WBPaper00031376
WBPaper00031851
WBPaper00032123
WBPaper00032231
WBPaper00032387
WBPaper00032740
WBPaper00033026
WBPaper00033637
WBPaper00033678
WBPaper00035054
WBPaper00035144
WBPaper00036249
WBPaper00037283
WBPaper00038057
WBPaper00038293
WBPaper00038491
WBPaper00039103
WBPaper00039881
WBPaper00040243
WBPaper00040433
WBPaper00041209
WBPaper00042228
WBPaper00042543
WBPaper00042756
WBPaper00043145
WBPaper00043233
WBPaper00043728
WBPaper00043942
WBPaper00044205
WBPaper00045076
WBPaper00045696
WBPaper00045775
WBPaper00046671
WBPaper00046973
WBPaper00047030
WBPaper00047547
WBPaper00047736
WBPaper00047992
WBPaper00048226
WBPaper00048254
WBPaper00048474
WBPaper00050610
WBPaper00051852
WBPaper00054455
WBPaper00054478
WBPaper00054980
WBPaper00055090
WBPaper00055144
WBPaper00056369
WBPaper00056678
WBPaper00056988
WBPaper00057005
WBPaper00057196
WBPaper00057476
WBPaper00057708
WBPaper00057916
WBPaper00057931
WBPaper00058465
WBPaper00058472
WBPaper00059531
WBPaper00059545
WBPaper00059578
WBPaper00059627
WBPaper00059895
WBPaper00060398
WBPaper00060507
WBPaper00061190
WBPaper00061409
WBPaper00061852
WBPaper00061891
WBPaper00062017
WBPaper00063171
WBPaper00063897
WBPaper00064317
WBPaper00064733
WBPaper00064979
WBPaper00065115
WBPaper00065243
WBPaper00065666
RemarkSequence connection from [Labrousse AM, van der Bliek AM]
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