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WormBase Tree Display for Gene: WBGene00017982

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Name Class

WBGene00017982SMapS_parentSequenceF32D1
IdentityVersion2
NameCGC_namehpo-18Paper_evidenceWBPaper00038231
Person_evidenceWBPerson26
Sequence_nameF32D1.2
Molecular_nameF32D1.2
F32D1.2.1
CE09866
Other_nameCELE_F32D1.2Accession_evidenceNDBBX284605
Public_namehpo-18
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
226 Apr 2011 13:31:47WBPerson2970Name_changeCGC_namehpo-18
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhpo
Allele (18)
StrainWBStrain00037472
RNASeq_FPKM (74)
GO_annotation00027726
00027727
00027728
00123253
00123254
00123255
Contained_in_operonCEOP5052
Ortholog (18)
ParalogWBGene00019880Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00022582Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven mitochondrial ATP synthesis. Predicted to be located in mitochondrial inner membrane. Predicted to be part of mitochondrial proton-transporting ATP synthase complex, catalytic sector F(1). Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 3. Is an ortholog of human ATP5F1E (ATP synthase F1 subunit epsilon) and ATP5F1EP2 (ATP synthase F1 subunit epsilon pseudogene 2).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:0060332Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:838)
Molecular_infoCorresponding_CDSF32D1.2
Corresponding_transcriptF32D1.2.1
Other_sequence (21)
Associated_featureWBsf652566
WBsf233569
Experimental_infoRNAi_result (23)
Expr_patternExpr1013457
Expr1037738
Expr1150007
Expr2012560
Expr2030797
Drives_constructWBCnstr00026867
Construct_productWBCnstr00026867
Microarray_results (20)
Expression_cluster (115)
InteractionWBInteraction000008398
WBInteraction000008399
WBInteraction000008400
WBInteraction000008401
WBInteraction000037062
WBInteraction000151571
WBInteraction000208867
WBInteraction000212163
WBInteraction000251315
WBInteraction000257530
WBInteraction000280434
WBInteraction000283332
WBInteraction000306256
WBInteraction000308733
WBInteraction000311583
WBInteraction000330143
WBInteraction000331927
WBInteraction000348582
WBInteraction000387085
WBInteraction000391749
WBInteraction000416305
WBInteraction000431730
WBInteraction000536368
WBInteraction000536381
WBInteraction000536395
WBInteraction000537148
WBInteraction000539676
WBInteraction000554006
WBInteraction000566397
WBInteraction000566676
WBInteraction000569370
WBInteraction000572238
WBInteraction000578094
WBInteraction000578539
WBInteraction000583433
Map_infoMapVPosition-5.88245Error0.011872
PositivePositive_cloneF32D1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00028999
WBPaper00038491
WBPaper00055090
WBPaper00060452
WBPaper00061870
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