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WormBase Tree Display for Gene: WBGene00010167

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Name Class

WBGene00010167SMapS_parentSequenceF56H6
IdentityVersion2
NameCGC_namebgnt-1.6Person_evidenceWBPerson2136
WBPerson5364
Sequence_nameF56H6.6
Molecular_nameF56H6.6
F56H6.6.1
CE16134
Other_nameCELE_F56H6.6Accession_evidenceNDBBX284601
Public_namebgnt-1.6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
209 Oct 2015 09:56:12WBPerson2970Name_changeCGC_namebgnt-1.6
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classbgnt
Allele (61)
StrainWBStrain00037592
RNASeq_FPKM (74)
Ortholog (33)
ParalogWBGene00008290Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00008491Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00009032Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00015982Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00010694Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00017723Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00011779Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00010716Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
Structured_descriptionAutomated_descriptionEnriched in germ line and in male based on RNA-seq studies. Is affected by several genes including pmk-1; npr-1; and pgl-1 based on tiling array; microarray; and RNA-seq studies. Is affected by ten chemicals including tryptophan; Tunicamycin; and allantoin based on microarray and RNA-seq studies. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A13. Human B4GAT1 enables glucuronosyltransferase activity. Is predicted to encode a protein with the following domain: Glycosyl-transferase for dystroglycan. 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_CDSF56H6.6
Corresponding_transcriptF56H6.6.1
Associated_featureWBsf220423
Experimental_infoRNAi_resultWBRNAi00003833Inferred_automaticallyRNAi_primary
WBRNAi00032991Inferred_automaticallyRNAi_primary
WBRNAi00048786Inferred_automaticallyRNAi_primary
Expr_patternExpr1028109
Expr1152535
Drives_constructWBCnstr00031617
Construct_productWBCnstr00031617
Microarray_results (14)
Expression_cluster (76)
Interaction (21)
Map_infoMapIPosition13.1105
PositivePositive_cloneF56H6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
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