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WormBase Tree Display for Gene: WBGene00001115

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Name Class

WBGene00001115SMapS_parentSequenceF47G6
IdentityVersion1
NameCGC_namedyb-1Person_evidenceWBPerson571
Sequence_nameF47G6.1
Molecular_nameF47G6.1a
F47G6.1a.1
CE26812
F47G6.1b
CE49501
F47G6.1c
CE49545
F47G6.1b.1
F47G6.1c.1
F47G6.1c.2
Other_nameCELE_F47G6.1Accession_evidenceNDBBX284601
Public_namedyb-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:23WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdyb
Allele (184)
StrainWBStrain00024337
WBStrain00024338
WBStrain00024339
WBStrain00024341
WBStrain00024342
RNASeq_FPKM (74)
GO_annotation (30)
Ortholog (41)
Paralog (13)
Structured_descriptionConcise_descriptiondyb-1 encodes a homolog of mammalian alpha-dystrobrevin (DTNA); DYB-1 physically interacts with DYS-1/dystrophin in vitro and CTN-1/alpha-catulinand and DYS-1/dystrophin in vivo.Paper_evidenceWBPaper00004614
WBPaper00005175
WBPaper00041089
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated02 Aug 2012 00:00:00
Automated_descriptionEnables acetylcholine transmembrane transporter activity and cytoskeletal protein binding activity. Involved in several processes, including muscle cell cellular homeostasis; positive regulation of cholinergic synaptic transmission; and sarcomere organization. Located in plasma membrane. Part of dystrobrevin complex. Expressed in body wall musculature; non-striated muscle; somatic nervous system; and tail neurons. Used to study Duchenne muscular dystrophy. Human ortholog(s) of this gene implicated in left ventricular noncompaction. Is an ortholog of human DTNA (dystrobrevin alpha).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:11723
Potential_modelDOID:0060480Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3057)
DOID:0050700Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3057)
Modifies_diseaseDOID:11723
Modifies_disease_in_annotationWBDOannot00000424
Models_disease_assertedWBDOannot00000094
Molecular_infoCorresponding_CDSF47G6.1a
F47G6.1b
F47G6.1c
Corresponding_transcriptF47G6.1a.1
F47G6.1b.1
F47G6.1c.1
F47G6.1c.2
Other_sequence (18)
Associated_featureWBsf982710
WBsf217219
WBsf217220
Experimental_infoRNAi_resultWBRNAi00047688Inferred_automaticallyRNAi_primary
WBRNAi00116485Inferred_automaticallyRNAi_primary
WBRNAi00003704Inferred_automaticallyRNAi_primary
WBRNAi00030225Inferred_automaticallyRNAi_primary
WBRNAi00078381Inferred_automaticallyRNAi_primary
Expr_patternExpr858
Expr9898
Expr12348
Expr1027186
Expr1030711
Expr1151527
Expr2011124
Expr2029360
Drives_constructWBCnstr00009573
WBCnstr00009574
WBCnstr00013378
WBCnstr00018328
Construct_productWBCnstr00009573
WBCnstr00009574
WBCnstr00013378
WBCnstr00018328
WBCnstr00020431
AntibodyWBAntibody00000352
Microarray_results (21)
Expression_cluster (104)
Interaction (73)
Map_infoMapIPosition-14.6127Error0.012384
PositivePositive_cloneF47G6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_data
Reference (33)
MethodGene