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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
AlleleWBVar02144606Inferred_automaticallyFrom strain object: EU2893
WBVar00425348
WBVar00425349
WBVar00425350
WBVar01499365
WBVar02133920
WBVar00250125
WBVar01499395
WBVar01499396
WBVar01953979
WBVar00910971
WBVar01499242
WBVar00910972
WBVar00910973
WBVar00910974
WBVar00910975
WBVar00910976
WBVar00910977
WBVar00910978
WBVar00910979
WBVar00910980
WBVar00910981
WBVar00910982
WBVar00910983
WBVar00910984
WBVar00910985
WBVar00910986
WBVar00910987
WBVar00910988
WBVar00910989
WBVar00910990
WBVar00572503
WBVar01499633
WBVar01515893
WBVar01515894
WBVar00246223
WBVar01966290
WBVar00189040
WBVar02144605
WBVar01500245
WBVar00425343
WBVar00425344
WBVar00425345
WBVar00425346
WBVar00425347
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
Reference (93)
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