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WormBase Tree Display for Gene: WBGene00001032

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Name Class

WBGene00001032SMapS_parentSequenceK02G10
IdentityVersion1
NameCGC_namednj-14Person_evidenceWBPerson625
Sequence_nameK02G10.8
Molecular_nameK02G10.8a
K02G10.8a.1
CE04708
K02G10.8b
CE45638
K02G10.8b.1
Other_nameCELE_K02G10.8Accession_evidenceNDBBX284606
Public_namednj-14
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_info (10)
Disease_infoExperimental_modelDOID:14503Homo sapiensPaper_evidenceWBPaper00045410
Accession_evidenceOMIM162350
Curator_confirmedWBPerson324
Date_last_updated24 Apr 2017 00:00:00
Potential_modelDOID:0110720Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16235)
Disease_relevanceMutations in human DNAJC5 are implicated in adult onset neuronal lipofuscinosis (ANCL; Kufs disease and Parry disease), a neurodegenerative disorder characterised by progressive neuronal dysfunction and premature death; DNAJC5 encodes an evolutionarily conserved member of the DnaJ/Hsp40 family of molecular chaperones known as cysteine string protein (CSP); in C. elegans, mutants of dnj-14 (tm3223, ok237), which is orthologous to human DNAJC5, show reduced life-span, impaired locomotion, reduced neurotransmission and impaired chemosensation; older dnj-14 animals exhibited neuronal abnormalities like loss of neuronal cell bodies, reduction in the number of visible neurites, and the presence of contorted neuronal processes; use of this dnj-14 model identified resveratrol as a compound that could extend dnj-14 mutant lifespan, partially rescue the neurodegeneration phenotype and significantly ameliorate the chemotaxis defects of dnj-14 mutants; this resveratrol activity was mimicked by phosphodiesterase inhibition and independent of SIR-2.1/Sirtuin, unlike in other C. elegans neurodegeneration models where resveratrol activity was shown to be sir-2.1 dependent.Homo sapiensPaper_evidenceWBPaper00045410
Accession_evidenceOMIM611203
Curator_confirmedWBPerson324
Date_last_updated24 Apr 2017 00:00:00
Models_disease_assertedWBDOannot00000331
WBDOannot00000409
WBDOannot00000410
Molecular_infoCorresponding_CDSK02G10.8a
K02G10.8b
Corresponding_transcriptK02G10.8a.1
K02G10.8b.1
Other_sequence (30)
Associated_featureWBsf653929
WBsf670453
WBsf982161
WBsf237308
WBsf237309
WBsf237310
WBsf237311
Experimental_infoRNAi_resultWBRNAi00016500Inferred_automaticallyRNAi_primary
WBRNAi00106560Inferred_automaticallyRNAi_primary
WBRNAi00106561Inferred_automaticallyRNAi_primary
WBRNAi00106329Inferred_automaticallyRNAi_primary
WBRNAi00033900Inferred_automaticallyRNAi_primary
WBRNAi00076542Inferred_automaticallyRNAi_primary
WBRNAi00049772Inferred_automaticallyRNAi_primary
Expr_patternExpr1021089
Expr1030644
Expr1153487
Expr2010988
Expr2029226
Drives_constructWBCnstr00042947
Regulate_expr_clusterWBPaper00048567:dnj-14_downregulated
WBPaper00048567:dnj-14_upregulated
Microarray_resultsSMD_K02G10.8
175242_at
185615_at
A_12_P116411
A_12_P159745
A_12_P159746
A_12_P159747
A_12_P159748
A_12_P159749
Aff_K02G10.8
GPL13394_WBGene00001032
GPL13914_K02G10.8
GPL14144_K02G10.8_178-237_0.916_8_B
GPL14144_K02G10.8_263-322_0.939_3_A
GPL14144_K02G10.8_81-140_0.904_11_C
GPL19516_CGZ0011674
GPL19516_CGZ0027502
GPL19516_CGZ0027503
GPL21109_K02G10.8a
GPL21109_K02G10.8b
GPL3518_CE04708
GPL8304_CE_WBGene00001032_A
GPL8304_CE_WBGene00001032_C
GPL8673_K02G10_8P00066
GPL8673_K02G10_8P00274
GPL8673_K02G10_8P00574
GPL9450_K02G10.8
cea2.p.149047
Expression_cluster (120)
Interaction (44)
Map_infoMapXPosition-6.83097Error0.016329
PositivePositive_cloneK02G10Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4264
5084
5264
Pseudo_map_position
Reference (14)
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