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WormBase Tree Display for Gene: WBGene00009773

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Name Class

WBGene00009773SMapS_parentSequenceF46B6
IdentityVersion2
NameCGC_namelipl-2Person_evidenceWBPerson3759
WBPerson7490
WBPerson545
Sequence_nameF46B6.8
Molecular_nameF46B6.8
F46B6.8.1
CE05874
Other_nameCELE_F46B6.8Accession_evidenceNDBBX284605
Public_namelipl-2
DB_infoDatabaseAceViewgene5K273
WormQTLgeneWBGene00009773
WormFluxgeneWBGene00009773
NDBlocus_tagCELE_F46B6.8
PanthergeneCAEEL|WormBase=WBGene00009773|UniProtKB=Q20449
familyPTHR11005
NCBIgene185840
RefSeqproteinNM_073126.4
TrEMBLUniProtAccQ20449
UniProt_GCRPUniProtAccQ20449
OMIMgene613497
613924
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
219 Jul 2010 13:43:13WBPerson2970Name_changeCGC_namelipl-2
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlipl
AlleleWBVar01038853
WBVar01038854
WBVar01038855
WBVar01038856
WBVar01038857
WBVar01499355
WBVar01499356
WBVar00467334
WBVar00467335
WBVar00467336
WBVar00467337
WBVar01590069
WBVar01500129
WBVar01499056
WBVar00213880
WBVar01863694
WBVar01863695
WBVar00257580
WBVar00257582
WBVar01499316
WBVar01038845
WBVar01038846
WBVar01038847
WBVar01038848
WBVar01038849
WBVar01038850
WBVar01038851
WBVar01038852
WBVar00252829
RNASeq_FPKM (74)
GO_annotation00068196
00068197
00117373
00117374
Ortholog (64)
ParalogWBGene00008510Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00022642Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00010062Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00020016Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00019376Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00021963Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00013050Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable hydrolase activity, acting on ester bonds. Predicted to be involved in lipid catabolic process. 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_CDSF46B6.8
Corresponding_transcriptF46B6.8.1
Other_sequence (16)
Associated_featureWBsf647111
WBsf232297
Experimental_infoRNAi_resultWBRNAi00032350Inferred_automaticallyRNAi_primary
WBRNAi00102885Inferred_automaticallyRNAi_primary
WBRNAi00015069Inferred_automaticallyRNAi_primary
WBRNAi00047500Inferred_automaticallyRNAi_primary
WBRNAi00114802Inferred_automaticallyRNAi_primary
Expr_patternExpr1023504
Expr1034274
Expr1151337
Expr2013205
Expr2031437
Drives_constructWBCnstr00017677
WBCnstr00031933
Construct_productWBCnstr00031933
Microarray_results (16)
Expression_cluster (354)
Interaction (71)
Map_infoMapVPosition2.19757Error0.000312
PositivePositive_cloneF46B6Inferred_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