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WormBase Tree Display for Gene: WBGene00007325

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Name Class

WBGene00007325SMapS_parentSequenceC05C9
IdentityVersion1
NameSequence_nameC05C9.1
Molecular_nameC05C9.1
C05C9.1.1
CE33968
Other_nameCELE_C05C9.1Accession_evidenceNDBBX284606
Public_nameC05C9.1
DB_infoDatabaseAceViewgeneXL779
WormQTLgeneWBGene00007325
WormFluxgeneWBGene00007325
NDBlocus_tagCELE_C05C9.1
PanthergeneCAEEL|WormBase=WBGene00007325|UniProtKB=Q17654
familyPTHR10504
NCBIgene259726
RefSeqproteinNM_077462.4
TREEFAMTREEFAM_IDTF315617
TrEMBLUniProtAccQ17654
UniProt_GCRPUniProtAccQ17654
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:47WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (55)
RNASeq_FPKM (74)
GO_annotation00058819
00115483
Ortholog (29)
ParalogWBGene00020563Caenorhabditis 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 and severe acute respiratory syndrome. Is an ortholog of human BPI (bactericidal permeability increasing protein); BPIFC (BPI fold containing family C); and 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_CDSC05C9.1
Corresponding_CDS_historyC05C9.1:wp101
Corresponding_transcriptC05C9.1.1
Associated_featureWBsf718699
WBsf1006922
WBsf236352
WBsf236353
Experimental_infoRNAi_resultWBRNAi00028485Inferred_automaticallyRNAi_primary
WBRNAi00039716Inferred_automaticallyRNAi_primary
WBRNAi00066536Inferred_automaticallyRNAi_primary
WBRNAi00010189Inferred_automaticallyRNAi_primary
Expr_patternExpr1022770
Expr1033153
Expr1143814
Expr2000456
Expr2018679
Drives_constructWBCnstr00033830
Construct_productWBCnstr00033830
Microarray_results (19)
Expression_cluster (128)
Interaction (46)
Map_infoPositivePositive_cloneC05C9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX2.86045
ReferenceWBPaper00042257
WBPaper00055090
MethodGene