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WormBase Tree Display for Gene: WBGene00020481

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Name Class

WBGene00020481SMapS_parentSequenceT13C2
IdentityVersion2
NameCGC_namegldi-2Person_evidenceWBPerson6609
WBPerson1816
Sequence_nameT13C2.6
Molecular_name (12)
Other_nameCELE_T13C2.6Accession_evidenceNDBBX284602
Public_namegldi-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
205 May 2023 12:43:53WBPerson51134Name_changeCGC_namegldi-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgldi
Allele (42)
StrainWBStrain00055214
RNASeq_FPKM (74)
GO_annotation00022613
00022614
00022615
00125113
Ortholog (51)
ParalogWBGene00008779Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00003071Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003072Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003738Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004374Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008609Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015083Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019756Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00019811Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable calcium ion binding activity. Predicted to be involved in endocytosis. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; artery disease (multiple); autistic disorder; and cerebellar ataxia, mental retardation and dysequlibrium syndrome. Is an ortholog of human LDLR (low density lipoprotein receptor); LRP8 (LDL receptor related protein 8); and VLDLR (very low density lipoprotein receptor).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_model (12)
Molecular_infoCorresponding_CDST13C2.6a
T13C2.6b
T13C2.6c
T13C2.6d
Corresponding_CDS_historyT13C2.6a:wp121
T13C2.6b:wp121
Corresponding_transcriptT13C2.6a.1
T13C2.6b.1
T13C2.6c.1
T13C2.6d.1
Other_sequence (47)
Associated_featureWBsf657714
WBsf657715
WBsf988248
WBsf1012423
WBsf221509
WBsf221510
WBsf221511
Experimental_infoRNAi_resultWBRNAi00053257Inferred_automaticallyRNAi_primary
WBRNAi00018668Inferred_automaticallyRNAi_primary
Expr_patternExpr1010844
Expr1038930
Expr1156839
Expr2006146
Expr2024361
Drives_constructWBCnstr00025109
Construct_productWBCnstr00025109
Microarray_results (28)
Expression_cluster (141)
InteractionWBInteraction000540409
WBInteraction000549323
WBInteraction000567718
WBInteraction000570396
WBInteraction000579405
WBInteraction000583497
Map_infoMapIIPosition0.107754
PositivePositive_cloneT13C2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027373
WBPaper00038491
WBPaper00055090
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