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WormBase Tree Display for Gene: WBGene00007687

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Name Class

WBGene00007687SMapS_parentSequenceC18E9
IdentityVersion1
NameSequence_nameC18E9.7
Molecular_nameC18E9.7
C18E9.7.1
CE52583
Other_nameCELE_C18E9.7Accession_evidenceNDBBX284602
Public_nameC18E9.7
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (46)
RNASeq_FPKM (74)
Ortholog (30)
ParalogWBGene00002915Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00011326Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00017013Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020516Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionEnriched in arcade cell; excretory gland cell; pharyngeal muscle cell; 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 microarray; tiling array; and RNA-seq studies. Is affected by sixteen chemicals including 1-methylnicotinamide; D-glucose; and stavudine based on RNA-seq and microarray studies. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome and vesicoureteral reflux. Human TNXB enables collagen fibril binding activity. Is predicted to encode a protein with the following domains: Fibronectin type III superfamily; TM proximal of protein tyrosine phosphatase, receptor type J; PTPRJ, transmembrane domain; Fibronectin type III; Immunoglobulin-like fold; and Fibronectin type III domain. Is an ortholog of human TNXA (tenascin XA (pseudogene)) and TNXB (tenascin XB).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:9620Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11976)
DOID:13359Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11976)
Molecular_infoCorresponding_CDSC18E9.7
Corresponding_CDS_historyC18E9.7:wp263
Corresponding_transcriptC18E9.7.1
Other_sequenceAS08763
ACC05160_1
MHC09111_1
ACC34413_1
MH10960
ASC04679_1
FC551183.1
FC551769.1
JI212309.1
Acan_isotig14345
Associated_featureWBsf665870
WBsf665871
WBsf717750
WBsf988890
WBsf988891
WBsf1012779
WBsf1012780
WBsf223579
Experimental_infoRNAi_resultWBRNAi00011009Inferred_automaticallyRNAi_primary
WBRNAi00081689Inferred_automaticallyRNAi_primary
WBRNAi00040956Inferred_automaticallyRNAi_primary
Expr_patternExpr1016580
Expr1033322
Expr1144999
Expr2000984
Expr2019203
Drives_constructWBCnstr00033554
Construct_productWBCnstr00033554
Microarray_results (19)
Expression_cluster (184)
Interaction (56)
Map_infoPositivePositive_cloneC18E9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionII0.946824
ReferenceWBPaper00053423
MethodGene