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WormBase Tree Display for Gene: WBGene00020563

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Name Class

WBGene00020563SMapS_parentSequenceT19C3
IdentityVersion1
NameSequence_nameT19C3.5
Molecular_nameT19C3.5
T19C3.5.1
CE54124
Other_nameCELE_T19C3.5Accession_evidenceNDBBX284603
Public_nameT19C3.5
DB_infoDatabaseAceViewgene3B242
WormQTLgeneWBGene00020563
WormFluxgeneWBGene00020563
NDBlocus_tagCELE_T19C3.5
PanthergeneCAEEL|WormBase=WBGene00020563|UniProtKB=Q10011
familyPTHR10504
NCBIgene188587
RefSeqproteinNM_001381695.1
SwissProtUniProtAccQ10011
TREEFAMTREEFAM_IDTF315617
UniProt_GCRPUniProtAccQ10011
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (78)
RNASeq_FPKM (74)
GO_annotation00055881
00125171
Ortholog (32)
ParalogWBGene00007325Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00003812Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008512Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008652Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015544Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015545Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00016951Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00018403Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022627Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable lipid binding activity. Predicted to be located in extracellular space. Human ortholog(s) of this gene implicated in Crohn's disease; atherosclerosis; and severe acute respiratory syndrome. Is an ortholog of several human genes including BPI (bactericidal permeability increasing protein); LBP (lipopolysaccharide binding protein); and PLTP (phospholipid transfer protein).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:8778Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1095)
DOID:2945Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:1095)
DOID:1936Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9093)
Molecular_infoCorresponding_CDST19C3.5
Corresponding_CDS_historyT19C3.5:wp275
Corresponding_transcriptT19C3.5.1
Other_sequence (15)
Associated_featureWBsf650805
WBsf991106
WBsf991107
WBsf991108
WBsf991109
WBsf1014099
WBsf1014100
WBsf1014101
WBsf1014102
WBsf226115
Experimental_infoRNAi_resultWBRNAi00035657Inferred_automaticallyRNAi_primary
WBRNAi00022448Inferred_automaticallyRNAi_primary
WBRNAi00053508Inferred_automaticallyRNAi_primary
WBRNAi00006632Inferred_automaticallyRNAi_primary
Expr_patternExpr1012355
Expr1038964
Expr1157075
Expr2006248
Expr2024466
Drives_constructWBCnstr00025048
Construct_productWBCnstr00025048
Microarray_results (19)
Expression_cluster (116)
InteractionWBInteraction000328718
WBInteraction000452521
Map_infoPositivePositive_cloneT19C3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIII-26.4808
ReferenceWBPaper00038491
WBPaper00055090
MethodGene