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WormBase Tree Display for Gene: WBGene00017763

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Name Class

WBGene00017763SMapS_parentSequenceF23H11
IdentityVersion2
NameCGC_namecrls-1Person_evidenceWBPerson8897
Sequence_nameF23H11.9
Molecular_nameF23H11.9a
F23H11.9a.1
CE09617
F23H11.9b
CE37763
F23H11.9b.1
Other_nameCELE_F23H11.9Accession_evidenceNDBBX284603
Public_namecrls-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
226 Feb 2009 11:04:20WBPerson9133Name_changeCGC_namecrls-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcrls
Allele (45)
RNASeq_FPKM (74)
GO_annotation (23)
Contained_in_operonCEOP3048
Ortholog (35)
ParalogWBGene00019255Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptioncrls-1 encodes a cardiolipin synthase; by homology, CRLS-1 is predicted to catalyze cardiolipin biosynthesis from phosphatidylglycerol and cytidinediphosphate-diacylglycerol, and loss of crls-1 activity results in reduced levels of cardiolipin and elevated levels of phosphatidylglycerol; in C. elegans, crls-1 activity is required for normal germ cell mitochondrial membrane potential and cristae morphology, as well as for germ cell proliferation.Paper_evidenceWBPaper00040537
Curator_confirmedWBPerson1843
Date_last_updated21 Dec 2011 00:00:00
Automated_descriptionEnables cardiolipin synthase activity. Involved in cardiolipin biosynthetic process; regulation of cell population proliferation; and regulation of mitochondrial membrane potential. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in combined oxidative phosphorylation deficiency 57. Is an ortholog of human CRLS1 (cardiolipin synthase 1).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:0070430Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16148)
Molecular_infoCorresponding_CDSF23H11.9a
F23H11.9b
Corresponding_CDS_historyF23H11.9:wp135
Corresponding_transcriptF23H11.9a.1
F23H11.9b.1
Other_sequence (35)
Associated_featureWBsf666549
WBsf666550
WBsf666551
WBsf991186
WBsf226155
Experimental_infoRNAi_resultWBRNAi00013835Inferred_automaticallyRNAi_primary
WBRNAi00111229Inferred_automaticallyRNAi_primary
WBRNAi00023724Inferred_automaticallyRNAi_primary
WBRNAi00023212Inferred_automaticallyRNAi_primary
WBRNAi00045448Inferred_automaticallyRNAi_primary
WBRNAi00006523Inferred_automaticallyRNAi_primary
WBRNAi00023437Inferred_automaticallyRNAi_primary
WBRNAi00024011Inferred_automaticallyRNAi_primary
Expr_patternExpr1024443
Expr1037628
Expr1149367
Expr2010533
Expr2028773
Drives_constructWBCnstr00027039
Construct_productWBCnstr00027039
Microarray_results (22)
Expression_cluster (54)
Interaction (69)
Map_infoMapIIIPosition-25.3228Error0.030952
PositivePositive_cloneF23H11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00034409
WBPaper00036608
WBPaper00036609
WBPaper00038491
WBPaper00039610
WBPaper00040537
WBPaper00042257
WBPaper00050263
WBPaper00055090
WBPaper00056678
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