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WormBase Tree Display for Gene: WBGene00002015

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Name Class

WBGene00002015SMapS_parentSequenceT27E4
IdentityVersion1
NameCGC_namehsp-16.1Person_evidenceWBPerson36
Sequence_nameT27E4.8
Molecular_nameT27E4.8
T27E4.8.1
CE14249
Other_namehsp-16
CELE_T27E4.8Accession_evidenceNDBBX284605
Public_namehsp-16.1
DB_infoDatabaseAceViewgene5J568
WormQTLgeneWBGene00002015
WormFluxgeneWBGene00002015
NDBlocus_tagCELE_T27E4.8
PanthergeneCAEEL|WormBase=WBGene00002015|UniProtKB=P34696
familyPTHR45640
NCBIgene179286
RefSeqproteinNM_072953.5
SwissProtUniProtAccP34696
UniProt_GCRPUniProtAccP34696
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhsp
AlleleWBVar01499903
WBVar01500129
WBVar00091863
WBVar01499419
WBVar01499420
WBVar01499056
WBVar01499249
WBVar01499316
StrainWBStrain00004819
WBStrain00004820
WBStrain00030548
WBStrain00030720
WBStrain00030838
In_clusterHSP16A
RNASeq_FPKM (74)
GO_annotation00044149
00044150
00044151
00044152
00044153
00044154
00105765
00105800
00106135
00106136
Ortholog (91)
Paralog (17)
Structured_descriptionConcise_descriptionhsp-16.1 encodes a 16-kD heat shock protein (HSP) that is a member of the hsp16/hsp20/alphaB-crystallin (HSP16) family of heat shock proteins, and that is identical to the protein encoded by hsp-16.11; an hsp-16.1 reporter fusion, expressed broadly but most strongly in muscle and hypodermis, is induced solely in response to heat shock or other environmental stresses; expression is detectable in somatic tissues in post-gastrulation embryos, all larval stages, and in adults; HSP-16.1 is likely to function as a passive ligand temporarily preventing unfolded proteins from aggregating.Paper_evidenceWBPaper00001187
WBPaper00001497
WBPaper00002665
WBPaper00004424
WBPaper00013029
WBPaper00013239
WBPaper00013280
Curator_confirmedWBPerson1843
Date_last_updated05 Nov 2004 00:00:00
Automated_descriptionPredicted to enable unfolded protein binding activity. Involved in defense response to Gram-negative bacterium and response to heat. Located in Golgi medial cisterna. Expressed in several structures, including coelomocyte; enteric muscle; intestine; pharynx; and ventral nerve cord.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_infoDisease_relevanceC. elegans is an effective model system to study heat-related pathologies like heat stroke; in elegans, a small heat shock protein (sHSP), HSP-16.1 has a protective effect against heat-induced necrosis; HSP-16.1 localizes to the golgi and functions together with the PMR-1/PMR1 Ca2+ and Mn2+ transporting ATPase, and NUCB-1/Nucleobindin1, a golgi-located calcium-buffering protein, to maintain calcium homeostasis, under heat stroke; overexpresiion of pmr-1/PMR1 is sufficient to promote survival after heat stroke, bypassing both HSF-1 and HSP-16.1, indicating that PMR-1/PMR1 functions downstream of both these genes.Homo sapiensPaper_evidenceWBPaper00041564
Curator_confirmedWBPerson324
Date_last_updated29 May 2013 00:00:00
Molecular_infoCorresponding_CDST27E4.8
Corresponding_transcriptT27E4.8.1
Other_sequence (60)
Associated_featureWBsf977958Paper_evidenceWBPaper00000918
WBsf977959Paper_evidenceWBPaper00000918
WBsf977962
WBsf1000813
WBsf234177
WBsf234178
Experimental_infoRNAi_result (21)
Expr_patternExpr1381
Expr1384
Expr10597
Expr11025
Expr15516
Expr1157862
Expr2012617
Expr2030853
Drives_construct (37)
Construct_productWBCnstr00010254
WBCnstr00017024
WBCnstr00019264
WBCnstr00036521
WBCnstr00042207
AntibodyWBAntibody00000049
WBAntibody00001859
Microarray_results (24)
Expression_cluster (245)
Interaction (92)
WBProcessWBbiopr:00000050
Map_infoMapVPosition1.9236Error0.000891
PositivePositive_cloneT27E4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4419
5342
Pseudo_map_position
Reference (121)
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