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WormBase Tree Display for Gene: WBGene00015982

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Name Class

WBGene00015982SMapS_parentSequenceC18G1
IdentityVersion2
NameCGC_namebgnt-1.4Person_evidenceWBPerson2136
WBPerson5364
Sequence_nameC18G1.3
Molecular_nameC18G1.3a
C18G1.3a.1
CE44423
C18G1.3b
CE44363
C18G1.3b.1
Other_nameCELE_C18G1.3Accession_evidenceNDBBX284605
Public_namebgnt-1.4
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
209 Oct 2015 09:56:12WBPerson2970Name_changeCGC_namebgnt-1.4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classbgnt
Allele (62)
RNASeq_FPKM (74)
GO_annotation00021958
Ortholog (44)
ParalogWBGene00008290Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00008491Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00009032Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00010167Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00010694Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00010716Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00011779Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00017723Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be located in membrane. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A13. Is an ortholog of human B4GAT1 (beta-1,4-glucuronyltransferase 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:0111238Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:15685)
Molecular_infoCorresponding_CDSC18G1.3a
C18G1.3b
Corresponding_CDS_historyC18G1.3:wp188
C18G1.3c:wp246
Corresponding_transcriptC18G1.3a.1
C18G1.3b.1
Associated_featureWBsf661237
Experimental_infoRNAi_resultWBRNAi00040970Inferred_automaticallyRNAi_primary
WBRNAi00012400Inferred_automaticallyRNAi_primary
WBRNAi00016625Inferred_automaticallyRNAi_primary
Expr_patternExpr1015241
Expr1145013
Microarray_results (12)
Expression_cluster (74)
Interaction (55)
Map_infoMapVPosition-4.24231
PositivePositive_cloneC18G1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029024
WBPaper00038491
WBPaper00055090
WBPaper00065080
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