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WormBase Tree Display for Gene: WBGene00006493

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Name Class

WBGene00006493SMapS_parentSequenceR09A8
IdentityVersion2
NameCGC_nameivns-1Person_evidenceWBPerson293
Sequence_nameR09A8.3
Molecular_nameR09A8.3
R09A8.3.1
CE03539
R09A8.3.2
Other_nametag-147Person_evidenceWBPerson201
CELE_R09A8.3Accession_evidenceNDBBX284606
Public_nameivns-1
DB_infoDatabaseAceViewgeneXN244
WormQTLgeneWBGene00006493
WormFluxgeneWBGene00006493
NDBlocus_tagCELE_R09A8.3
PanthergeneCAEEL|WormBase=WBGene00006493|UniProtKB=Q21854
familyPTHR24412
NCBIgene181410
RefSeqproteinNM_077708.9
TrEMBLUniProtAccQ21854
UniProt_GCRPUniProtAccQ21854
OMIMgene609209
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
211 Oct 2017 16:33:09WBPerson1983Name_changeCGC_nameivns-1
Other_nametag-147
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classivns
Allele (189)
StrainWBStrain00002827
WBStrain00033011
WBStrain00035813
RNASeq_FPKM (74)
Ortholog (34)
Paralog (11)
Structured_descriptionAutomated_descriptionEnriched in body wall musculature; intestine; neurons; pharynx; and somatic gonad precursor based on Chronogram; RNA-seq; and single-cell RNA-seq studies. Is affected by several genes including daf-2; skn-1; and daf-12 based on tiling array; proteomic; RNA-seq; and microarray studies. Is affected by ten chemicals including stavudine; Tunicamycin; and bortezomib based on RNA-seq and microarray studies. Human ortholog(s) of this gene implicated in immunodeficiency 70. Is predicted to encode a protein with the following domains: Galactose oxidase/kelch, beta-propeller; Kelch-type beta propeller; Kelch motif; SKP1/BTB/POZ domain superfamily; Kelch repeat type 1; BTB/POZ domain; and BTB/Kelch-associated. Is an ortholog of human IVNS1ABP (influenza virus NS1A 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:0112005Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16951)
Molecular_infoCorresponding_CDSR09A8.3
Corresponding_transcriptR09A8.3.1
R09A8.3.2
Other_sequence (55)
Associated_feature (18)
Experimental_infoRNAi_resultWBRNAi00017621Inferred_automaticallyRNAi_primary
WBRNAi00034761Inferred_automaticallyRNAi_primary
WBRNAi00051584Inferred_automaticallyRNAi_primary
WBRNAi00000350Inferred_automaticallyRNAi_primary
Expr_patternChronogram1704
Expr1016812
Expr1032656
Expr1155256
Expr2017229
Expr2035365
Drives_constructWBCnstr00003352
WBCnstr00034338
Construct_productWBCnstr00034338
Microarray_results (21)
Expression_cluster (172)
InteractionWBInteraction000282181
WBInteraction000376618
WBInteraction000538932
WBInteraction000551487
WBInteraction000557847
WBInteraction000568464
WBInteraction000571931
WBInteraction000573593
WBInteraction000579706
Map_infoMapXPosition7.26648Error0.059523
PositivePositive_cloneR09A8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00055785
WBPaper00061547
RemarkMap position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene