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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_sequenceFF678415.1
FK803290.1
FK804490.1
FK808037.1
FK809806.1
AI308687.1
FK804584.1
FK802230.1
FG977006.1
Tcol_isotig04242
CRC00970_1
Tcol_isotig26350
FK804896.1
FK805086.1
FK809641.1
FK806949.1
FK809214.1
FK805604.1
ES410115.1
FK805689.1
GW409780.1
ES741220.1
Hbac_contig01129
Tcol_isotig04243
FK801344.1
SR02510
FK802710.1
HBC13421_1
FK809160.1
FK809225.1
HBC08431_1
FK807963.1
EX013558.1
FF678061.1
EX014706.1
FF678231.1
FK803799.1
Tcol_isotig26360
CBC08489_1
FK808695.1
FK807506.1
HBC00672_1
FK802641.1
FF678055.1
FF678970.1
MHC00206_1
EX011439.1
FK809899.1
FK806413.1
FK800057.1
FK803795.1
Oden_isotig16753
JO471433.1
FK803891.1
FF679135.1
FF678566.1
FK806471.1
FK801196.1
HBC03683_1
FK808921.1
FF678890.1
FF679149.1
PPC08803_1
FK800077.1
FK803241.1
FK806144.1
FK807731.1
FK803096.1
FK803727.1
PPC10507_1
FK805731.1
FK808630.1
FK807956.1
FK804709.1
FK806357.1
FK804244.1
FF678457.1
FK804293.1
CJC02839_1
FK803203.1
BMC05296_1
FK805399.1
FK800122.1
ES411748.1
FF678112.1
FF678802.1
FK801444.1
FK800434.1
EX915684.1
FK802135.1
FK807079.1
HBC26088_1
FK800133.1
PSC00362_1
SSC01739_1
OVC02550_1
FK804711.1
ES742110.1
Tcol_isotig15653
FK807785.1
FF678327.1
FF679097.1
FK800924.1
FK810027.1
FF679255.1
HBC27096_1
FK806931.1
FK809769.1
FK810024.1
FK805778.1
FK808965.1
FK800485.1
FF678066.1
FK803607.1
FK809348.1
FK804808.1
ES739292.1
FK809586.1
FK809425.1
SS00136
FK805147.1
HBC02312_1
MH02573
FK801838.1
FK803830.1
FK808612.1
FK806817.1
FF678804.1
FK800116.1
FK802364.1
EX914945.1
FK809316.1
FK800009.1
ES413265.1
FK802875.1
FK807373.1
FK803520.1
FK802694.1
FG981071.1
CR03875
EX012916.1
FF678786.1
FK803396.1
FK807448.1
FK800034.1
FK805022.1
FF678194.1
FK807072.1
FF678638.1
FK801150.1
FK802007.1
ES409432.1
CBC08864_1
FK806985.1
FK803205.1
FK799913.1
FK806684.1
FK809891.1
Associated_featureWBsf647418
WBsf661943
WBsf232714
Experimental_infoRNAi_result (6)
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