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WormBase Tree Display for Gene: WBGene00002023

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Name Class

WBGene00002023SMapS_parentSequenceC09B8
IdentityVersion1
NameCGC_namehsp-25Person_evidenceWBPerson36
Sequence_nameC09B8.6
Molecular_nameC09B8.6a
C09B8.6a.1
CE02466
C09B8.6b
CE33558
C09B8.6c
CE37953
C09B8.6b.1
C09B8.6c.1
C09B8.6c.2
Other_nameHSP25Paper_evidenceWBPaper00036199
CELE_C09B8.6Accession_evidenceNDBBX284606
Public_namehsp-25
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhsp
Allele (81)
RNASeq_FPKM (74)
GO_annotation00059380
00059381
00059382
00059383
00059384
00059385
00059386
Ortholog (35)
Paralog (17)
Structured_descriptionConcise_descriptionhsp-25 encodes a member of the small heat shock family of proteins; HSP-25 is expressed throughout development and in vitro, exhibits chaperone activity; HSP-25 localizes to: 1) dense bodies and M lines in body wall muscle, 2) the lining of the pharynx, and 3) to cell-cell junctions in the spermathecal wall; consistent with a role in myofibril organization, HSP-25 binds vinculin and alpha-actinin in vitro.Paper_evidenceWBPaper00003970
WBPaper00013029
Curator_confirmedWBPerson1843
Date_last_updated02 Mar 2007 00:00:00
Automated_descriptionPredicted to enable unfolded protein binding activity. Predicted to be involved in protein refolding and response to heat. Located in M band and striated muscle dense body. Expressed in body wall musculature; gonad; pharynx; and spermatheca. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease axonal type 2L and distal hereditary motor neuronopathy type 2A. Is an ortholog of human HSPB8 (heat shock protein family B (small) member 8).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:0111208Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:30171)
DOID:0110174Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:30171)
Molecular_infoCorresponding_CDSC09B8.6a
C09B8.6b
C09B8.6c
Corresponding_transcriptC09B8.6a.1
C09B8.6b.1
C09B8.6c.1
C09B8.6c.2
Other_sequence (120)
Associated_feature (19)
Experimental_infoRNAi_resultWBRNAi00097033Inferred_automaticallyRNAi_primary
WBRNAi00106387Inferred_automaticallyRNAi_primary
WBRNAi00076103Inferred_automaticallyRNAi_primary
WBRNAi00040161Inferred_automaticallyRNAi_primary
WBRNAi00033415Inferred_automaticallyRNAi_primary
WBRNAi00010508Inferred_automaticallyRNAi_primary
Expr_patternExpr1087
Expr1088
Expr4163
Expr15507
Expr1018056
Expr1031178
Expr1144237
Expr2012624
Expr2030860
Drives_constructWBCnstr00036514
WBCnstr00042198
Construct_productWBCnstr00036514
WBCnstr00042198
AntibodyWBAntibody00000270
Microarray_results (33)
Expression_cluster (201)
Interaction (48)
Map_infoMapXPosition-3.82033Error0.011016
PositivePositive_cloneC09B8Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4562
Pseudo_map_position
ReferenceWBPaper00013029
WBPaper00036199
WBPaper00038491
WBPaper00055090
WBPaper00060685
WBPaper00061766
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