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WormBase Tree Display for Gene: WBGene00017241

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Name Class

WBGene00017241SMapS_parentSequenceF08C6
IdentityVersion2
NameCGC_namepcyt-1Person_evidenceWBPerson1711
Sequence_nameF08C6.2
Molecular_nameF08C6.2a
F08C6.2a.1
CE30937
F08C6.2b
CE39144
F08C6.2b.1
Other_nameCELE_F08C6.2Accession_evidenceNDBBX284606
Public_namepcyt-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:58WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
220 Apr 2011 10:05:24WBPerson2970Name_changeCGC_namepcyt-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpcyt
Allele (156)
StrainWBStrain00031168
WBStrain00037474
RNASeq_FPKM (74)
GO_annotation (15)
Ortholog (42)
ParalogWBGene00017878Caenorhabditis elegansFrom_analysisTreeFam
WBGene00021215Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016531Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021352Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionpcyt-1 encodes a lipid-activated CTP:phosphocholine cytidylyltransferase (CCT), with CCT activity in vitro; recombinant PCYT-1 is most activated by a 1:1 mixture of phosphatidylcholine:oleate vesicles; an inhibitory 21-residue segment (residues 246-266) is critical for specific activation of PCYT-1 by lipids, since deletion or mutation of this segment causes PCYT-1 to be constitutively active without its normal lipid substrate.Paper_evidenceWBPaper00004651
WBPaper00004877
WBPaper00005654
WBPaper00035321
Curator_confirmedWBPerson1843
WBPerson567
Date_last_updated14 Oct 2011 00:00:00
Automated_descriptionEnables choline-phosphate cytidylyltransferase activity. Involved in phosphatidylcholine biosynthetic process. Expressed in head. Human ortholog(s) of this gene implicated in spondylometaphyseal dysplasia with cone-rod dystrophy. Is an ortholog of human PCYT1A (phosphate cytidylyltransferase 1A, choline) and PCYT1B (phosphate cytidylyltransferase 1B, choline).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:0112300Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8754)
Molecular_infoCorresponding_CDSF08C6.2a
F08C6.2b
Corresponding_CDS_historyF08C6.2:wp149
Corresponding_transcriptF08C6.2a.1
F08C6.2b.1
Other_sequence (77)
Associated_feature (20)
Experimental_infoRNAi_result (34)
Expr_pattern (7)
Drives_constructWBCnstr00002991
WBCnstr00027460
Construct_productWBCnstr00027460
Microarray_results (25)
Expression_cluster (177)
Interaction (73)
Map_infoMapXPosition-1.49196
PositivePositive_cloneF08C6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027269
WBPaper00027740
WBPaper00031072
WBPaper00031805
WBPaper00034497
WBPaper00035321
WBPaper00038491
WBPaper00040189
WBPaper00040386
WBPaper00042257
WBPaper00044247
WBPaper00050085
WBPaper00055090
WBPaper00056988
WBPaper00061547
WBPaper00065123
PictureWBPicture0000013096
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