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WormBase Tree Display for Gene: WBGene00003068

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Name Class

WBGene00003068EvidencePerson_evidenceWBPerson1068
SMapS_parentSequenceT27C10
IdentityVersion1
NameCGC_namelrk-1Person_evidenceWBPerson1315
Sequence_nameT27C10.6
Molecular_nameT27C10.6
T27C10.6.1
CE41939
Other_nameLRRK2Paper_evidenceWBPaper00045582
CELE_T27C10.6Accession_evidenceNDBBX284601
Public_namelrk-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:30WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlrk
Allele (160)
RNASeq_FPKM (74)
GO_annotation (28)
Ortholog (36)
Paralog (12)
Structured_descriptionConcise_descriptionlrk-1 encodes the sole C. elegans homolog of the leucine-rich repeat kinases, LRRK1 and the familial Parkinsonism gene PARK8/LRRK2; in C. elegans, lrk-1 is required for polarized localization of synaptic vesicle proteins to presynaptic regions; LRK-1 functions antagonistically to PINK-1 to regulate oxidative and endoplasmic reticulum stress response as well as neurite outgrowth; LRK-1 is widely expressed and localizes to the Golgi apparatus.Paper_evidenceWBPaper00029175
WBPaper00032949
WBPaper00034758
WBPaper00036154
WBPaper00040114
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated14 Sep 2011 00:00:00
Automated_descriptionPredicted to enable metal ion binding activity; protein kinase activity; and purine ribonucleoside triphosphate binding activity. Involved in several processes, including axon extension involved in axon guidance; cellular localization; and negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway. Located in Golgi apparatus and neuronal cell body. Expressed in hermaphrodite distal tip cell; neurons; pharynx; and vulva. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in osteosclerotic metaphyseal dysplasia. Is an ortholog of human LRRK1 (leucine rich repeat kinase 1).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_evidenceWBPaper00035592
WBPaper00034758
Accession_evidenceOMIM607060
Curator_confirmedWBPerson324
Date_last_updated19 Jan 2018 00:00:00
Potential_modelDOID:0081111Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18608)
Disease_relevanceMutations in human PARK8/LRRK2 (a GTPase regulated kinase) are the most common cause of inherited Parkinson''s disease (PD); C. elegans is used as a model system to study the genetic interactions and molecular functions of PARK protein orthologs; overexpression of either wild-type or mutant (G2019S) LRRK2 enhanced dopaminergic neuron degeneration, while knockdown of the elegans lrk-1 increased toxicity in the nematode to rotenone, a broad spectrum pesticide that interferes with the mitochondrial electron-transport chain; lrk-1/LRRK2 may act together with sek-1/MKK6 and pmk-1/p38 and antagonistic to pink-1/PINK1, another PD-related gene, the loss-of-function of which results in dopaminergic neurons, to modulate the cellular stress response.Homo sapiensPaper_evidenceWBPaper00035592
WBPaper00035922
WBPaper00032949
Accession_evidenceOMIM607060
609007
Curator_confirmedWBPerson324
Date_last_updated08 Jan 2014 00:00:00
Models_disease_in_annotationWBDOannot00000208
Models_disease_assertedWBDOannot00000473
Molecular_infoCorresponding_CDST27C10.6
Corresponding_CDS_historyT27C10.6:wp94
T27C10.6:wp173
T27C10.6:wp185
Corresponding_transcriptT27C10.6.1
Other_sequence (12)
Associated_featureWBsf664892
WBsf717574
WBsf985118
WBsf985119
WBsf985120
WBsf985121
WBsf220297
WBsf220298
WBsf220299
Experimental_infoRNAi_result (14)
Expr_patternExpr4597
Expr8648
Expr12733
Expr1026978
Expr1031445
Expr1157834
Expr2013267
Expr2031498
Drives_constructWBCnstr00005648
WBCnstr00012104
WBCnstr00013419
WBCnstr00036251
Construct_productWBCnstr00005648
WBCnstr00012104
WBCnstr00013419
WBCnstr00022702
WBCnstr00036251
AntibodyWBAntibody00002686
Microarray_results (24)
Expression_cluster (96)
Interaction (40)
Map_infoMapIPosition5.69269
PositivePositive_cloneT27C10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4480
Pseudo_map_position
Reference (54)
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
[140923 pad] Modified Map position as it was a reverse physical that could not be fixed by automated methods.
MethodGene