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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
ReferenceWBPaper00027722
WBPaper00038491
WBPaper00042257
WBPaper00042295
WBPaper00045355
WBPaper00052391
WBPaper00055090
WBPaper00056804
WBPaper00057084
WBPaper00059258
WBPaper00059755
WBPaper00064093
WBPaper00065331
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