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WormBase Tree Display for Gene: WBGene00006643

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Name Class

WBGene00006643SMapS_parentSequenceC02F12
IdentityVersion1
NameCGC_nametsp-17Person_evidenceWBPerson522
Sequence_nameC02F12.1
Molecular_name (15)
Other_nameCELE_C02F12.1Accession_evidenceNDBBX284606
Public_nametsp-17
DB_infoDatabaseAceViewgeneXE303
WormQTLgeneWBGene00006643
WormFluxgeneWBGene00006643
NDBlocus_tagCELE_C02F12.1
PanthergeneCAEEL|WormBase=WBGene00006643|UniProtKB=Q11098
familyPTHR19282
NCBIgene192067
RefSeqproteinNM_001313386.3
NM_001383547.2
NM_001313384.4
NM_001313385.3
NM_001136448.4
SwissProtUniProtAccQ11098
UniProt_GCRPUniProtAccQ11098
OMIMgene300096
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtsp
Allele (50)
StrainWBStrain00034688
WBStrain00034689
WBStrain00034690
WBStrain00034691
WBStrain00034693
WBStrain00034695
WBStrain00034696
WBStrain00034670
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (35)
Paralog (20)
Structured_descriptionAutomated_descriptionEnables D2 dopamine receptor binding activity. Involved in cellular response to paraquat; negative regulation of response to oxidative stress; and regulation of dopamine uptake involved in synaptic transmission. Located in neuron projection; perinuclear region of cytoplasm; and plasma membrane. Expressed in several structures, including NSM; body wall musculature; dopaminergic neurons; hermaphrodite gonad; and vulva. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability 58. Is an ortholog of human TSPAN3 (tetraspanin 3) and TSPAN7 (tetraspanin 7).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:1289Homo sapiensPaper_evidenceWBPaper00046082
Curator_confirmedWBPerson324
Date_last_updated04 Feb 2015 00:00:00
DOID:14330Homo sapiensPaper_evidenceWBPaper00053621
Curator_confirmedWBPerson324
Date_last_updated04 Mar 2019 00:00:00
Potential_modelDOID:0112024Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11854)
Models_disease_in_annotationWBDOannot00000344
Models_disease_assertedWBDOannot00000638
Molecular_infoCorresponding_CDSC02F12.1a
C02F12.1b
C02F12.1c
C02F12.1d
C02F12.1e
Corresponding_CDS_historyC02F12.1:wp107
C02F12.1:wp192
C02F12.1a:wp246
C02F12.1b:wp225
Corresponding_transcriptC02F12.1a.1
C02F12.1b.1
C02F12.1c.1
C02F12.1d.1
C02F12.1e.1
Other_sequence (21)
Associated_featureWBsf662619
WBsf1004692
WBsf1004693
WBsf235515
Experimental_infoRNAi_resultWBRNAi00039430Inferred_automaticallyRNAi_primary
WBRNAi00010002Inferred_automaticallyRNAi_primary
WBRNAi00028350Inferred_automaticallyRNAi_primary
Expr_patternExpr12508
Expr1013023
Expr1032759
Expr1143544
Expr2017546
Expr2035684
Drives_constructWBCnstr00021630
WBCnstr00034244
Construct_productWBCnstr00021630
WBCnstr00034244
Microarray_results (26)
Expression_cluster (129)
Interaction (35)
Map_infoMapXPosition-9.80493Error0.009623
PositivePositive_cloneC02F12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00046082
WBPaper00047946
WBPaper00053621
WBPaper00055090
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