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WormBase Tree Display for Gene: WBGene00002028

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Name Class

WBGene00002028SMapS_parentSequenceF08B4
IdentityVersion1
NameCGC_namehst-1Person_evidenceWBPerson1831
Sequence_nameF08B4.6
Molecular_nameF08B4.6
F08B4.6.1
CE46914
Other_nameCELE_F08B4.6Accession_evidenceNDBBX284604
Public_namehst-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhst
Allele (43)
StrainWBStrain00036041
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (53)
ParalogWBGene00002030Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00044303Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionhst-1 encodes the C. elegans ortholog of N-deacetylase/N-sulfotransferase (NDST), a bifunctional enzyme that catalyzes N-deacetylation and N-sulfation of N-acetylglucosamine residues in heparan sulfate; loss of hst-1 activity has been reported to result in embryonic lethality at various stages of development, defects in ventral neuroblast migrations during epidermal enclosure, and cessation of egg production in injected hermaphrodites.Paper_evidenceWBPaper00004540
WBPaper00027618
Curator_confirmedWBPerson1843
Date_last_updated09 Apr 2008 00:00:00
Automated_descriptionPredicted to enable [heparan sulfate]-glucosamine N-sulfotransferase activity and deacetylase activity. Predicted to be involved in heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process. Predicted to be located in Golgi apparatus. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 46. Is an ortholog of several human genes including NDST1 (N-deacetylase and N-sulfotransferase 1); NDST2 (N-deacetylase and N-sulfotransferase 2); and NDST3 (N-deacetylase and N-sulfotransferase 3).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:0081210Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7680)
Molecular_infoCorresponding_CDSF08B4.6
Corresponding_CDS_historyF08B4.6:wp92
F08B4.6:wp229
Corresponding_transcriptF08B4.6.1
Other_sequence (40)
Associated_featureWBsf652010
WBsf230453
WBsf230454
Experimental_infoRNAi_resultWBRNAi00012868Inferred_automaticallyRNAi_primary
WBRNAi00043971Inferred_automaticallyRNAi_primary
WBRNAi00062194Inferred_automaticallyRNAi_primary
WBRNAi00085699Inferred_automaticallyRNAi_primary
WBRNAi00030634Inferred_automaticallyRNAi_primary
Expr_patternExpr1010220
Expr1031183
Expr1147945
Expr2012633
Expr2030869
Drives_constructWBCnstr00036511
Construct_productWBCnstr00036511
Microarray_results (20)
Expression_cluster (113)
Interaction (16)
Map_infoMapIVPosition3.93215Error0.002647
PositivePositive_cloneF08B4Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4874
4940
Pseudo_map_position
Reference (12)
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