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WormBase Tree Display for Gene: WBGene00011771

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Name Class

WBGene00011771SMapS_parentSequenceT14G8
IdentityVersion1
NameSequence_nameT14G8.3
Molecular_nameT14G8.3
T14G8.3.1
CE37407
Other_nameCELE_T14G8.3Accession_evidenceNDBBX284606
Public_nameT14G8.3
DB_infoDatabaseAceViewgeneXN487
WormQTLgeneWBGene00011771
WormFluxgeneWBGene00011771
NDBlocus_tagCELE_T14G8.3
PanthergeneCAEEL|WormBase=WBGene00011771|UniProtKB=Q22515
familyPTHR45639
NCBIgene181422
RefSeqproteinNM_001029742.7
TrEMBLUniProtAccQ22515
UniProt_GCRPUniProtAccQ22515
OMIMgene601746
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:53WBPerson1971EventImportedInitial conversion from CDS class of WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (142)
StrainWBStrain00031455
RNASeq_FPKM (74)
GO_annotation00075469
00075470
00075471
00075472
00075473
00075474
00075475
00105757
00119003
00119004
Ortholog (43)
Paralog (11)
Structured_descriptionConcise_descriptionT14G8.3 encodes an ortholog of hypoxia-upregulated vertebrate proteins such as human HYOU1; T14G8.3, its C. elegans paralog T24H7.2, and HYOU1 are ER resident hsp70 family molecular chaperone homologs; the grp (glucose regulated protein) 170 family is a collection of related large hsp70 chaperones confined to the ER; members of this family are present in all eukaryotes, participating in a wide range of cellular functions.Paper_evidenceWBPaper00028288
WBPaper00028291
WBPaper00028319
WBPaper00028321
Curator_confirmedWBPerson567
Date_last_updated18 Jul 2005 00:00:00
Automated_descriptionPredicted to enable adenyl-nucleotide exchange factor activity. Involved in IRE1-mediated unfolded protein response. Predicted to be part of endoplasmic reticulum chaperone complex. Human ortholog(s) of this gene implicated in immunodeficiency 59. Is an ortholog of human HYOU1 (hypoxia up-regulated 1).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:0111974Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16931)
Molecular_infoCorresponding_CDST14G8.3
Corresponding_CDS_historyT14G8.3:wp131
T14G8.3b:wp272
Corresponding_transcriptT14G8.3.1
Other_sequence (35)
Associated_feature (11)
Experimental_infoRNAi_resultWBRNAi00076679Inferred_automaticallyRNAi_primary
WBRNAi00001906Inferred_automaticallyRNAi_primary
WBRNAi00106355Inferred_automaticallyRNAi_primary
WBRNAi00035582Inferred_automaticallyRNAi_primary
WBRNAi00000500Inferred_automaticallyRNAi_primary
WBRNAi00053347Inferred_automaticallyRNAi_primary
WBRNAi00018730Inferred_automaticallyRNAi_primary
Expr_patternExpr1026039
Expr1035184
Expr1156932
Expr2006184
Expr2024400
Drives_constructWBCnstr00030402
Construct_productWBCnstr00030402
Microarray_results (25)
Expression_cluster (172)
Interaction (56)
Map_infoPositivePositive_cloneT14G8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX8.66255
ReferenceWBPaper00005432
WBPaper00026830
WBPaper00038491
WBPaper00041022
WBPaper00051015
WBPaper00055090
MethodGene