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WormBase Tree Display for Gene: WBGene00086546

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Name Class

WBGene00086546SMapS_parentSequenceC50C3
IdentityVersion3
NameCGC_nameinpp-5KAuthor_evidenceWBPerson555
Sequence_nameC50C3.7
Molecular_nameC50C3.7
C50C3.7.1
CE00123
Other_namecil-1Author_evidenceWBPerson555
CELE_C50C3.7Accession_evidenceNDBBX284603
Public_nameinpp-5K
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 Jun 2008 15:25:15WBPerson2970EventCreated
215 Dec 2010 16:15:12WBPerson2970EventAcquires_mergeWBGene00016802
310 Jul 2023 23:47:10WBPerson51134Name_changeCGC_nameinpp-5K
Other_namecil-1
Acquires_mergeWBGene00016802
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classinpp
Allele (29)
RNASeq_FPKM (74)
GO_annotation (25)
Contained_in_operonCEOP3484
Ortholog (45)
ParalogWBGene00006763Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007620Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00012016Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007912Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009264Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00012353Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionEnables phosphatidylinositol phosphate phosphatase activity. Acts upstream of or within with a positive effect on flagellated sperm motility. Located in several cellular components, including neuronal cell body; nucleus; and plasma membrane bounded cell projection. Expressed in PVDL and PVDR. Human ortholog(s) of this gene implicated in congenital muscular dystrophy with cataracts and intellectual disability. Is an ortholog of human INPP5J (inositol polyphosphate-5-phosphatase J) and INPP5K (inositol polyphosphate-5-phosphatase K).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:0080197Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:33882)
Molecular_infoCorresponding_CDSC50C3.7
Corresponding_transcriptC50C3.7.1
Other_sequenceCR00431
CBC10379_1
Dviv_isotig19742
CRC08417_1
Dviv_isotig19743
PPC15966_1
Associated_featureWBsf667137
WBsf667138
WBsf976241
WBsf976242
WBsf227087
WBsf227088
WBsf227089
WBsf227090
Experimental_infoRNAi_resultWBRNAi00005436Inferred_automaticallyRNAi_primary
WBRNAi00030018Inferred_automaticallyRNAi_primary
WBRNAi00012199Inferred_automaticallyRNAi_primary
WBRNAi00042876Inferred_automaticallyRNAi_primary
Expr_patternExpr12821
Expr13848
Expr1040416
Expr1146855
Expr2010014
Expr2028255
Drives_constructWBCnstr00023180
WBCnstr00040206
Construct_productWBCnstr00022884
WBCnstr00022885
WBCnstr00023180
WBCnstr00040206
Microarray_results (18)
Expression_cluster (109)
WBProcessWBbiopr:00000012
Map_infoMapIIIPosition-0.37497Error0.000172
PositivePositive_cloneC50C3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029208
WBPaper00031689
WBPaper00035231
WBPaper00054995
WBPaper00055090
WBPaper00061449
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