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WormBase Tree Display for Gene: WBGene00012328

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Name Class

WBGene00012328SMapS_parentSequenceW07G1
IdentityVersion1
NameSequence_nameW07G1.1
Molecular_nameW07G1.1
W07G1.1.1
CE38232
Other_nameCELE_W07G1.1Accession_evidenceNDBBX284602
Public_nameW07G1.1
DB_infoDatabaseAceViewgene2O226
WormQTLgeneWBGene00012328
WormFluxgeneWBGene00012328
NDBlocus_tagCELE_W07G1.1
PanthergeneCAEEL|WormBase=WBGene00012328|UniProtKB=Q9XUK4
familyPTHR23004
NCBIgene189278
RefSeqproteinNM_064516.2
TrEMBLUniProtAccQ9XUK4
UniProt_GCRPUniProtAccQ9XUK4
OMIMgene605755
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:53WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (100)
RNASeq_FPKM (74)
GO_annotation00101842
00101843
00119472
Ortholog (29)
ParalogWBGene00007374Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00012332Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be involved in intracellular signal transduction. Predicted to be located in microtubule and microtubule organizing center. Human ortholog(s) of this gene implicated in several diseases, including attention deficit hyperactivity disorder; autosomal recessive nonsyndromic deafness 66; and dyslexia. Is an ortholog of human DCDC2 (doublecortin domain containing 2) and DCDC2C (doublecortin domain containing 2C).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:0110517Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18141)
DOID:1094Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18141)
DOID:14268Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18141)
DOID:0111126Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18141)
DOID:4428Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18141)
Molecular_infoCorresponding_CDSW07G1.1
Corresponding_CDS_historyW07G1.1:wp140
Corresponding_transcriptW07G1.1.1
Other_sequenceCR01447
Associated_featureWBsf990554
WBsf990555
WBsf1013725
WBsf1013726
Experimental_infoRNAi_resultWBRNAi00103570Inferred_automaticallyRNAi_primary
WBRNAi00036361Inferred_automaticallyRNAi_primary
WBRNAi00054954Inferred_automaticallyRNAi_primary
WBRNAi00019702Inferred_automaticallyRNAi_primary
Expr_patternExpr1021441
Expr1158488
Expr2006843
Expr2025068
Drives_constructWBCnstr00029997
Construct_productWBCnstr00029997
Microarray_results (18)
Expression_cluster (41)
InteractionWBInteraction000189625
WBInteraction000202955
WBInteraction000212793
WBInteraction000220829
WBInteraction000236013
WBInteraction000240625
WBInteraction000288806
WBInteraction000370083
WBInteraction000458204
Map_infoPositivePositive_cloneW07G1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionII21.4234
ReferenceWBPaper00055090
MethodGene