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WormBase Tree Display for Gene: WBGene00018319

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Name Class

WBGene00018319SMapS_parentSequenceF41H10
IdentityVersion3
NameCGC_namehda-6Person_evidenceWBPerson260
WBPerson2136
Sequence_nameF41H10.6
Molecular_name (12)
Other_namehdac-6Paper_evidenceWBPaper00005214
Person_evidenceWBPerson2136
Y4C6B.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_F41H10.6Accession_evidenceNDBBX284604
Public_namehda-6
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:00WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
202 Nov 2009 10:01:13WBPerson9133Name_changeCGC_namehdac-6
312 Apr 2012 16:15:43WBPerson2970Name_changeCGC_namehda-6
Other_namehdac-6
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhda
Allele (90)
StrainWBStrain00033033
RNASeq_FPKM (74)
GO_annotation (14)
Contained_in_operonCEOP4679
CEOP4002
Ortholog (61)
ParalogWBGene00001837Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001838Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009663Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00219378Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00001834Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001835Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001836Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007953Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009657Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable histone deacetylase activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be part of histone deacetylase complex. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in several diseases, including cervix uteri carcinoma in situ; chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia; and polycystic liver disease. Is an ortholog of human HDAC6 (histone deacetylase 6).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_infoExperimental_modelDOID:14330Homo sapiensPaper_evidenceWBPaper00041253
Curator_confirmedWBPerson324
Date_last_updated18 Nov 2013 00:00:00
Potential_modelDOID:8991Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14064)
DOID:4947Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14064)
DOID:0112106Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14064)
DOID:0050770Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14064)
Disease_relevanceIn elegans, alpha-synuclein (alpha-syn) toxicity, implicated in Parkinson''s disease and other synucleinopathies, is modeled by expressing it from the dopamine transporter (dat-1) gene promotor in transgenic GFP worms, resulting in an age-dependent progressive loss of dopaminergic neurons; using this system, it was seen that the knock-down of specific candidate genes in elegans, that interact with catp-6/ATP13A2, resulted in significant enhancement of alpha-syn-induced dopaminergic neurodegeneration; these catp-6/ATP13A2 interactors include the elegans ortholog of histone deacetylase 6 (hda-6), coagulation factor II (thrombin) receptor (dop-2), AP2 associated kinase 1 (AAK1; sel-5) along with neuropeptide Y receptor Y1 (npr-4), and YIP1 interacting factor homolog A (yif-1).Homo sapiensPaper_evidenceWBPaper00041253
Curator_confirmedWBPerson324
Date_last_updated19 Nov 2013 00:00:00
Models_disease_in_annotationWBDOannot00000249
Molecular_infoCorresponding_CDSF41H10.6a
F41H10.6b
F41H10.6c
F41H10.6d
Corresponding_transcriptF41H10.6a.1
F41H10.6b.1
F41H10.6c.1
F41H10.6d.1
Other_sequence (43)
Associated_featureWBsf651797
WBsf996488
WBsf230078
WBsf230079
WBsf230080
Experimental_infoRNAi_result (11)
Expr_patternExpr1026528
Expr1037891
Expr1150910
Expr2012389
Expr2030625
Drives_constructWBCnstr00005977
WBCnstr00008472
WBCnstr00026611
Construct_productWBCnstr00008471
WBCnstr00026611
Regulate_expr_clusterWBPaper00056039:hda-6(ok3203)_downregulated
WBPaper00056039:hda-6(ok3203)_upregulated
Microarray_results (34)
Expression_cluster (114)
Interaction (44)
Map_infoMapIVPosition1.59535Error0.000683
PositivePositive_cloneF41H10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
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