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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)
Interaction (78)
Map_infoMapVPosition-19.9825
PositivePositive_cloneR11G11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00042257
WBPaper00042295
WBPaper00052391
WBPaper00055090
WBPaper00056804
WBPaper00057084
WBPaper00058665
WBPaper00059578
WBPaper00059755
WBPaper00061998
WBPaper00064634
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