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WormBase Tree Display for Gene: WBGene00010062

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Name Class

WBGene00010062SMapS_parentSequenceF54F3
IdentityVersion2
NameCGC_namelipl-1Person_evidenceWBPerson3759
WBPerson7490
WBPerson545
Sequence_nameF54F3.3
Molecular_nameF54F3.3
F54F3.3.1
CE18732
Other_nameCELE_F54F3.3Accession_evidenceNDBBX284605
Public_namelipl-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
219 Jul 2010 13:43:13WBPerson2970Name_changeCGC_namelipl-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlipl
Allele (32)
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (73)
ParalogWBGene00008510Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00009773Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00019376Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022642Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00020016Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00014770Caenorhabditis elegansFrom_analysismodENCODE_Pseudogenes
WBGene00021963Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013050Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable hydrolase activity, acting on ester bonds. Involved in lipid catabolic process. Located in lysosome. Expressed in intestine. 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_CDSF54F3.3
Corresponding_transcriptF54F3.3.1
Other_sequence (158)
Associated_featureWBsf647418
WBsf661943
WBsf232714
Experimental_infoRNAi_resultWBRNAi00048376Inferred_automaticallyRNAi_primary
WBRNAi00032814Inferred_automaticallyRNAi_primary
WBRNAi00102884Inferred_automaticallyRNAi_primary
WBRNAi00002279Inferred_automaticallyRNAi_primary
WBRNAi00015656Inferred_automaticallyRNAi_primary
WBRNAi00078262Inferred_automaticallyRNAi_primary
Expr_patternChronogram1974
Expr6184
Expr1016806
Expr1152165
Expr2013204
Expr2031436
Drives_constructWBCnstr00003635
WBCnstr00017676
WBCnstr00031698
Construct_productWBCnstr00031698
Microarray_results (20)
Expression_cluster (315)
Interaction (36)
Map_infoMapVPosition4.73223Error0.002129
PositivePositive_cloneF54F3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
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