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WormBase Tree Display for Gene: WBGene00008512

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Name Class

WBGene00008512SMapS_parentSequenceF01G10
IdentityVersion1
NameSequence_nameF01G10.10
Molecular_nameF01G10.10
F01G10.10.1
CE40351
Other_nameCELE_F01G10.10Accession_evidenceNDBBX284604
Public_nameF01G10.10
DB_infoDatabaseAceViewgene4L13
WormQTLgeneWBGene00008512
WormFluxgeneWBGene00008512
NDBlocus_tagCELE_F01G10.10
PanthergeneCAEEL|WormBase=WBGene00008512|UniProtKB=O17768
familyPTHR10504
NCBIgene177907
RefSeqproteinNM_069478.6
TREEFAMTREEFAM_IDTF317549
TrEMBLUniProtAccO17768
UniProt_GCRPUniProtAccO17768
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (45)
RNASeq_FPKM (74)
GO_annotation00030663
00116411
Ortholog (41)
ParalogWBGene00016951Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00008652Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00018403Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00015544Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00003812Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007325Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015545Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020563Caenorhabditis 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 and severe acute respiratory syndrome. Is an ortholog of human LBP (lipopolysaccharide binding 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)
Molecular_infoCorresponding_CDSF01G10.10
Corresponding_CDS_historyF01G10.10:wp162
Corresponding_transcriptF01G10.10.1
Other_sequence (19)
Associated_featureWBsf646295
Experimental_infoRNAi_resultWBRNAi00030547Inferred_automaticallyRNAi_primary
WBRNAi00043763Inferred_automaticallyRNAi_primary
WBRNAi00012743Inferred_automaticallyRNAi_primary
Expr_patternExpr1014887
Expr1033704
Expr1147741
Expr2002198
Expr2020419
Drives_constructWBCnstr00032908
Construct_productWBCnstr00032908
Microarray_results (19)
Expression_cluster (171)
Interaction (228)
Map_infoPositivePositive_cloneF01G10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionIV4.56406
ReferenceWBPaper00038491
WBPaper00055090
MethodGene