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WormBase Tree Display for Gene: WBGene00018943

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Name Class

WBGene00018943SMapS_parentSequenceF56C3
IdentityVersion2
NameCGC_namedgn-2Person_evidenceWBPerson345
Sequence_nameF56C3.6
Molecular_nameF56C3.6
F56C3.6.1
CE17897
Other_nameCELE_F56C3.6Accession_evidenceNDBBX284606
Public_namedgn-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:01WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
209 Feb 2005 16:32:53WBPerson2970Name_changeCGC_namedgn-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdgn
Allele (47)
StrainWBStrain00005033
WBStrain00005039
RNASeq_FPKM (74)
GO_annotation00036244
00036245
00036246
00036247
00036248
00036249
00036250
00123910
Ortholog (16)
ParalogWBGene00017221Caenorhabditis elegansFrom_analysisTreeFam
WBGene00000961Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable laminin binding activity. Predicted to be involved in axon guidance; morphogenesis of an epithelium; and nerve development. Predicted to be located in sarcolemma. Predicted to be part of dystroglycan complex. Human ortholog(s) of this gene implicated in Duchenne muscular dystrophy; Fukuyama congenital muscular dystrophy; autosomal recessive limb-girdle muscular dystrophy type 2D; autosomal recessive limb-girdle muscular dystrophy type 2P; bronchopulmonary dysplasia; congenital muscular dystrophy-dystroglycanopathy type A9; and inclusion body myositis. Is an ortholog of human DAG1 (dystroglycan 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:0110278Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:0050559Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:11723Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:3429Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:0110293Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:11650Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
DOID:0111232Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2666)
Molecular_infoCorresponding_CDSF56C3.6
Corresponding_transcriptF56C3.6.1
Associated_featureWBsf670110
WBsf1004022
WBsf1004023
WBsf1022260
WBsf1022261
Experimental_infoRNAi_resultWBRNAi00048661Inferred_automaticallyRNAi_primary
WBRNAi00032940Inferred_automaticallyRNAi_primary
WBRNAi00093028Inferred_automaticallyRNAi_primary
Expr_patternExpr1026871
Expr1152423
Expr2029107
Drives_constructWBCnstr00026176
Construct_productWBCnstr00026176
Microarray_results (17)
Expression_cluster (63)
InteractionWBInteraction000203122
WBInteraction000217819
WBInteraction000306215
WBInteraction000377236
WBInteraction000396771
Map_infoMapXPosition-18.2125Error0.051862
PositivePositive_cloneF56C3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5069
4744
Pseudo_map_position
ReferenceWBPaper00027231
WBPaper00027321
WBPaper00032446
WBPaper00040382
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