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WormBase Tree Display for Gene: WBGene00016468

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Name Class

WBGene00016468SMapS_parentSequenceC36B7
IdentityVersion1
NameSequence_nameC36B7.5
Molecular_nameC36B7.5a
C36B7.5a.1
CE53489
C36B7.5b
CE53156
C36B7.5b.1
Other_nameCELE_C36B7.5Accession_evidenceNDBBX284606
Public_nameC36B7.5
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (284)
StrainWBStrain00032430
RNASeq_FPKM (74)
Ortholog (36)
ParalogWBGene00000082Caenorhabditis elegansFrom_analysisTreeFam
WBGene00003252Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00011880Caenorhabditis elegansFrom_analysisPanther
WBGene00020567Caenorhabditis elegansFrom_analysisTreeFam
WBGene00017471Caenorhabditis elegansFrom_analysisPanther
WBGene00017376Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionEnriched in ADEshL; ADEshR; and sensory neurons based on RNA-seq and single-cell RNA-seq studies. Is affected by several genes including daf-16; daf-2; and skn-1 based on tiling array; microarray; and RNA-seq studies. Is affected by thirteen chemicals including 1-methylnicotinamide; D-glucose; and stavudine based on RNA-seq and microarray studies. Human ortholog(s) of this gene implicated in X-linked properdin deficiency and factor VIII deficiency. Is predicted to encode a protein with the following domains: Thrombospondin type-1 (TSP1) repeat; Thrombospondin type-1 (TSP1) repeat superfamily; and Thrombospondin type 1 domain. Is an ortholog of human CFP (complement factor properdin).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:0111768Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8864)
DOID:12134Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8864)
Molecular_infoCorresponding_CDSC36B7.5a
C36B7.5b
Corresponding_CDS_historyC36B7.5a:wp271
C36B7.5b:wp271
Corresponding_transcriptC36B7.5a.1
C36B7.5b.1
Other_sequenceHBC24641_1
AE04003
JI165394.1
AYC02258_1
ES409745.1
Associated_featureWBsf654105
WBsf654106
WBsf670682
WBsf1005725
WBsf1005726
WBsf1005727
WBsf1023187
Experimental_infoRNAi_resultWBRNAi00011683Inferred_automaticallyRNAi_primary
WBRNAi00042046Inferred_automaticallyRNAi_primary
Expr_patternExpr1020498
Expr1037064
Expr1146046
Expr2001472
Expr2019695
Drives_constructWBCnstr00028043
Construct_productWBCnstr00028043
Microarray_results (25)
Expression_cluster (133)
InteractionWBInteraction000354454
WBInteraction000391641
Map_infoPositivePositive_cloneC36B7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX-1.87044
ReferenceWBPaper00055090
WBPaper00064898
MethodGene