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WormBase Tree Display for Gene: WBGene00002031

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Name Class

WBGene00002031SMapS_parentSequenceY34B4A
IdentityVersion1
NameCGC_namehst-6Person_evidenceWBPerson1831
Sequence_nameY34B4A.3
Molecular_nameY34B4A.3
Y34B4A.3.1
CE32011
Other_nameY34B4A.eCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_Y34B4A.3Accession_evidenceNDBBX284606
Public_namehst-6
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhst
Allele (56)
StrainWBStrain00029287
WBStrain00029319
WBStrain00029330
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (46)
Structured_descriptionConcise_descriptionhst-6 encodes the C. elegans ortholog of the heparan sulfate modifying enzyme heparan 6O-sulfotransferase; by homology, HST-6 is predicted to function in heparan sulfate biosynthesis by catalyzing the chain-modifying sulfation of the C6 hydroxyl group of the glucosamine subunits; during development, hst-6 activity is required for normal body size and nervous system development; an hst-6::gfp transcriptional reporter fusion is expressed beginning at early embryonic stages and continuing through adulthood; expression in embryos is nearly ubiquitous with later expression primarily restricted to neuronal tissues.Paper_evidenceWBPaper00006471
WBPaper00029002
Curator_confirmedWBPerson1843
Date_last_updated26 Oct 2007 00:00:00
Automated_descriptionPredicted to enable heparan sulfate 6-O-sulfotransferase activity. Involved in heparan sulfate proteoglycan biosynthetic process, enzymatic modification and regulation of growth. Predicted to be located in membrane. Expressed in AIBL; AIBR; RIML; RIMR; and neurons. Human ortholog(s) of this gene implicated in Paganini-Miozzo syndrome and hypogonadotropic hypogonadism 15 with or without anosmia. Is an ortholog of human HS6ST1 (heparan sulfate 6-O-sulfotransferase 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:0111843Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19133)
DOID:0090075Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5201)
Molecular_infoCorresponding_CDSY34B4A.3
Corresponding_CDS_historyY34B4A.3:wp86
Corresponding_transcriptY34B4A.3.1
Other_sequence (28)
Associated_featureWBsf648093
WBsf662771
WBsf1005223
WBsf235701
Experimental_infoRNAi_resultWBRNAi00020191Inferred_automaticallyRNAi_primary
WBRNAi00055817Inferred_automaticallyRNAi_primary
Expr_patternExpr2901
Expr12886
Expr1014721
Expr1031186
Expr1159347
Expr2012637
Expr2030873
Drives_constructWBCnstr00011014
WBCnstr00016152
WBCnstr00036509
Construct_productWBCnstr00005444
WBCnstr00005695
WBCnstr00005696
WBCnstr00005697
WBCnstr00005699
WBCnstr00005700
WBCnstr00005701
WBCnstr00005702
WBCnstr00005703
WBCnstr00036509
Microarray_results (17)
Expression_cluster (104)
Interaction (12)
Anatomy_functionWBbtf0285
Map_infoMapXPosition-5.86683Error0.040424
PositivePositive_cloneY34B4AInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4422
4502
Pseudo_map_position
ReferenceWBPaper00005236
WBPaper00005839
WBPaper00006129
WBPaper00006471
WBPaper00025387
WBPaper00026825
WBPaper00027618
WBPaper00029002
WBPaper00029024
WBPaper00032413
WBPaper00033254
WBPaper00033980
WBPaper00034029
WBPaper00035166
WBPaper00035477
WBPaper00035539
WBPaper00037286
WBPaper00038286
WBPaper00038491
WBPaper00039167
WBPaper00039168
WBPaper00039874
WBPaper00040941
WBPaper00045532
WBPaper00045569
WBPaper00050258
WBPaper00055090
WBPaper00061415
WBPaper00064400
RemarkSequence connection from [Turnbull J, Kinnunen T]. krb 13/11/01
Map 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