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WormBase Tree Display for Gene: WBGene00020016

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Name Class

WBGene00020016SMapS_parentSequenceR11G11
IdentityVersion2
NameCGC_namelipl-3Person_evidenceWBPerson3759
WBPerson7490
WBPerson545
Sequence_nameR11G11.14
Molecular_nameR11G11.14
R11G11.14.1
CE28762
Other_nameCELE_R11G11.14Accession_evidenceNDBBX284605
Public_namelipl-3
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:02WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 Jul 2010 13:43:13WBPerson2970Name_changeCGC_namelipl-3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlipl
Allele (186)
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (64)
ParalogWBGene00008510Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00009773Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010062Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00013050Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00019376Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022642Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00021963Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable hydrolase activity, acting on ester bonds. Involved in lipid catabolic process. Located in lysosome. Human ortholog(s) of this gene implicated in Wolman disease; autosomal recessive congenital ichthyosis 8; and cholesterol ester storage disease. Is an ortholog of several human genes including LIPA (lipase A, lysosomal acid type); LIPF (lipase F, gastric type); and LIPJ (lipase family member J).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:0080217Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6617)
DOID:14502Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6617)
DOID:14497Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6617)
DOID:0060717Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:23452)
Molecular_infoCorresponding_CDSR11G11.14
Corresponding_transcriptR11G11.14.1
Other_sequence (133)
Associated_featureWBsf233272
Experimental_infoRNAi_resultWBRNAi00017769Inferred_automaticallyRNAi_primary
WBRNAi00102886Inferred_automaticallyRNAi_primary
WBRNAi00115885Inferred_automaticallyRNAi_primary
WBRNAi00001388Inferred_automaticallyRNAi_primary
WBRNAi00034869Inferred_automaticallyRNAi_primary
WBRNAi00051811Inferred_automaticallyRNAi_primary
Expr_patternExpr1019660
Expr1155472
Drives_constructWBCnstr00017678
WBCnstr00025429
Construct_productWBCnstr00025429
Microarray_results (18)
Expression_cluster (218)
InteractionWBInteraction000104178
WBInteraction000104179
WBInteraction000135291
WBInteraction000213132
WBInteraction000237955
WBInteraction000245133
WBInteraction000253478
WBInteraction000253809
WBInteraction000256077
WBInteraction000265292
WBInteraction000286458
WBInteraction000291732
WBInteraction000294268
WBInteraction000304792
WBInteraction000305210
WBInteraction000317554
WBInteraction000317591
WBInteraction000317993
WBInteraction000318517
WBInteraction000322650
WBInteraction000324255
WBInteraction000329303
WBInteraction000330431
WBInteraction000332467
WBInteraction000337865
WBInteraction000342239
WBInteraction000343506
WBInteraction000345378
WBInteraction000346070
WBInteraction000347441
WBInteraction000348610
WBInteraction000349580
WBInteraction000350168
WBInteraction000352117
WBInteraction000355454
WBInteraction000357637
WBInteraction000359335
WBInteraction000366466
WBInteraction000376765
WBInteraction000378469
WBInteraction000378470
WBInteraction000381578
WBInteraction000382933
WBInteraction000386359
WBInteraction000389994
WBInteraction000391675
WBInteraction000392222
WBInteraction000392915
WBInteraction000397118
WBInteraction000399550
WBInteraction000404237
WBInteraction000404260
WBInteraction000406608
WBInteraction000410640
WBInteraction000412048
WBInteraction000413491
WBInteraction000417669
WBInteraction000421104
WBInteraction000426518
WBInteraction000433485
WBInteraction000434715
WBInteraction000435702
WBInteraction000436662
WBInteraction000440226
WBInteraction000443473
WBInteraction000444726
WBInteraction000446903
WBInteraction000449250
WBInteraction000452060
WBInteraction000452798
WBInteraction000456349
WBInteraction000457693
WBInteraction000460989
WBInteraction000465476
WBInteraction000472873
WBInteraction000473557
WBInteraction000520068
WBInteraction000520073
Map_infoMapVPosition-19.9825
PositivePositive_cloneR11G11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (12)
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