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WormBase Tree Display for Gene: WBGene00004035

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Name Class

WBGene00004035SMapS_parentSequenceY73F8A
IdentityVersion1
NameCGC_namepkd-2Person_evidenceWBPerson625
Sequence_nameY73F8A.1
Molecular_nameY73F8A.1
Y73F8A.1.1
CE38663
Other_namepdk-2
CELE_Y73F8A.1Accession_evidenceNDBBX284604
Public_namepkd-2
DB_infoDatabaseAceViewgene4P994
WormQTLgeneWBGene00004035
WormFluxgeneWBGene00004035
OMIMdisease613095
gene173910
NDBlocus_tagCELE_Y73F8A.1
PanthergeneCAEEL|WormBase=WBGene00004035|UniProtKB=Q9U1S7
familyPTHR10877
NCBIgene178424
RefSeqproteinNM_070437.5
SwissProtUniProtAccQ9U1S7
UniProt_GCRPUniProtAccQ9U1S7
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpkd
Allele (134)
StrainWBStrain00026468
WBStrain00030885
WBStrain00031062
WBStrain00031013
RNASeq_FPKM (74)
GO_annotation (66)
Ortholog (57)
ParalogWBGene00003058Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00016889Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionpkd-2 encodes a TRPP cation channel orthologous to human PKD2; pkd-2 is required for two aspects of male mating behavior: response to hermaphrodite contact and vulva location and acts with lov-1; PKD-2 is expressed in the cilia of three types of male-specific sensory neurons; EGL-44 and EGL-46 regulate cell-specific expression of lov-1 and pkd-2 to specify the behavioral function of the HOB neuron.Paper_evidenceWBPaper00003680
WBPaper00004854
WBPaper00006247
Curator_confirmedWBPerson567
Date_last_updated12 Aug 2011 00:00:00
Automated_descriptionEnables calcium channel activity. Involved in calcium ion transport; response to hermaphrodite contact; and vulval location. Located in several cellular components, including neuronal cell body; perinuclear region of cytoplasm; and plasma membrane bounded cell projection. Expressed in CEM; nerve ring; neurons; and ray. Used to study autosomal dominant polycystic kidney disease. Human ortholog(s) of this gene implicated in intracranial aneurysm; polycystic kidney disease 2; and retinal degeneration. Is an ortholog of human PKD2 (polycystin 2, transient receptor potential cation channel) and PKD2L1 (polycystin 2 like 1, transient receptor potential cation channel).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:898Homo sapiensPaper_evidenceWBPaper00003680
WBPaper00004854
Accession_evidenceOMIM613095
Curator_confirmedWBPerson324
Date_last_updated30 Apr 2018 00:00:00
Potential_modelDOID:0080322Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9009)
DOID:898Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9009)
DOID:0110859Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9009)
DOID:10941Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9009)
DOID:8466Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9009)
Disease_relevancelov-1 and pkd-2 encode the orthologs of human Polycystin-1 and Polycystin-2, which are mutated in autosomal dominant polycystic kidney disease; the polycystins regulate signaling involved in normal renal tubular structure and function; studies in the worm C. elegans have contributed extensively to the finding that cystic kidney diseases can be considered ciliopathies; in elegans lov-1 and pkd-2 are expressed in male ciliary neurons, are required for normal male mating behavior, do not seem to be required for ciliogenesis, and each polycystin may actually have a potential inhibitory function on the other for ciliary function; lov-1 and pkd-1 interact with a single-pass transmembrane protein, CWP-5, though the significance of this interaction for polycystic kidney disease is unknown.Homo sapiensPaper_evidenceWBPaper00038373
Accession_evidenceOMIM613095
173910
Curator_confirmedWBPerson324
Date_last_updated24 Jan 2012 00:00:00
Models_disease_in_annotationWBDOannot00000033
Models_disease_assertedWBDOannot00000514
Molecular_infoCorresponding_CDSY73F8A.1
Corresponding_CDS_historyY73F8A.1:wp90
Y73F8A.1:wp143
Corresponding_transcriptY73F8A.1.1
Other_sequenceCRC10242_1
CR05211
FK801188.1
JI174536.1
Associated_featureWBsf998698
WBsf998699
WBsf1018743
WBsf1018744
WBsf1018745
WBsf1018746
WBsf231243
Experimental_infoRNAi_resultWBRNAi00066584Inferred_automaticallyRNAi_primary
WBRNAi00000585Inferred_automaticallyRNAi_primary
WBRNAi00021407Inferred_automaticallyRNAi_primary
WBRNAi00021408Inferred_automaticallyRNAi_primary
WBRNAi00058373Inferred_automaticallyRNAi_primary
WBRNAi00112685Inferred_automaticallyRNAi_primary
WBRNAi00037811Inferred_automaticallyRNAi_primary
Expr_pattern (17)
Drives_construct (54)
Construct_product (11)
AntibodyWBAntibody00000407
WBAntibody00002558
WBAntibody00002633
Microarray_results (22)
Expression_cluster (66)
InteractionWBInteraction000001659
WBInteraction000003816
WBInteraction000003818
WBInteraction000003822
WBInteraction000003824
WBInteraction000005648
WBInteraction000005652
WBInteraction000008609
WBInteraction000028391
WBInteraction000030296
WBInteraction000030458
WBInteraction000031513
WBInteraction000113395
WBInteraction000113396
WBInteraction000113397
WBInteraction000113398
WBInteraction000126261
WBInteraction000126775
WBInteraction000127536
WBInteraction000139096
WBInteraction000150127
WBInteraction000161030
WBInteraction000165662
WBInteraction000166429
WBInteraction000170126
WBInteraction000175482
WBInteraction000179632
WBInteraction000179638
WBInteraction000183671
WBInteraction000207620
WBInteraction000416835
WBInteraction000473523
WBInteraction000501603
WBInteraction000501604
WBInteraction000501688
WBInteraction000501780
WBInteraction000501983
WBInteraction000502045
WBInteraction000502332
WBInteraction000502338
WBInteraction000502594
WBInteraction000502595
WBInteraction000502938
WBInteraction000502944
WBInteraction000503576
WBInteraction000503577
WBInteraction000503578
WBInteraction000504816
WBInteraction000504817
WBInteraction000504825
WBInteraction000505076
WBInteraction000517522
WBInteraction000517523
WBInteraction000517524
WBInteraction000517525
WBInteraction000517526
WBInteraction000517740
WBInteraction000517741
WBInteraction000517742
WBInteraction000525375
WBInteraction000532914
WBInteraction000543496
WBInteraction000556864
WBInteraction000556865
WBInteraction000556867
WBInteraction000557012
WBProcessWBbiopr:00000012
Map_infoMapIVPosition13.0445
PositivePositive_cloneY73F8AInferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4982
Pseudo_map_position
Reference (156)
RemarkThe use of the name pdk-2 for this gene was due to a typo in the original paper [krb 020128]
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
[140923 pad] Modified Map position as it was a reverse physical that could not be fixed by automated methods.
MethodGene