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WormBase Tree Display for Gene: WBGene00016103

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Name Class

WBGene00016103SMapS_parentSequenceC25F6
IdentityVersion2
NameCGC_namedpyd-1
Sequence_nameC25F6.3
Molecular_nameC25F6.3
C25F6.3.1
CE38489
Other_nameCELE_C25F6.3Accession_evidenceNDBBX284606
Public_namedpyd-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
203 Aug 2007 17:23:44WBPerson2970Name_changeCGC_namedpyd-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdpyd
Allele (67)
StrainWBStrain00037841
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (32)
ParalogWBGene00012326Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013376Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020932Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiondpyd-1 encodes the C. elegans ortholog of human DihydroPYrimidine Dehydrogenase (DPYD), which when mutated leads to thymine-uraciluria (OMIM:274270); DPYD-1 is the first and rate-limiting enzyme for uracil and thymine metabolism to 5,6-dihydrouracil and 5,6-dihydrothymine, respectively, and in humans, functions in metabolism of the anti-cancer pyrimidine antagonist 5-fluorouracil (5-FU); in C. elegans, loss of dpyd-1 activity via RNAi results in sensitivity (decreased survival) to 5-FU while conversely, DPYD-1 overexpression affords increased germ cell survivability to 5-FU.Paper_evidenceWBPaper00004637
WBPaper00013017
WBPaper00031988
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated10 Jul 2008 00:00:00
Automated_descriptionPredicted to enable NADP binding activity; dihydropyrimidine dehydrogenase (NADP+) activity; and uracil binding activity. Predicted to be involved in thymidine catabolic process; thymine catabolic process; and uracil catabolic process. Predicted to be located in cytosol. Human ortholog(s) of this gene implicated in several diseases, including acute lymphoblastic leukemia; dihydropyrimidine dehydrogenase deficiency; and gallbladder cancer. Is an ortholog of human DPYD (dihydropyrimidine dehydrogenase).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_model (4)
Molecular_infoCorresponding_CDSC25F6.3
Corresponding_CDS_historyC25F6.3:wp142
Corresponding_transcriptC25F6.3.1
Other_sequenceFC555671.1
Tcir_isotig08632
SRC00623_1
PPC16871_1
FC548069.1
PT02945
FC549122.1
XIC02970_1
FC547929.1
SR00505
MH07599
MH00860
FK804195.1
FC809775.1
ES410587.1
MI00158
Tcol_isotig11489
TDC02668_1
FC815113.1
FC548232.1
DN153193.1
Tcol_isotig26008
Oden_isotig18500
ASC07041_1
BXC02161_1
FC541046.1
DN153259.1
PPC01126_1
Tcir_isotig26143
Dviv_isotig19649
Tcol_isotig11490
CBC06068_1
PP02111
MI00795
HBC02426_1
JI164796.1
Hbac_isotig01416
FC555690.1
MH01742
Dviv_isotig25187
EX562930.1
Tcir_isotig30924
FC547342.1
MHC04535_1
Oden_isotig25174
MIC00965_1
FK802767.1
MIC01279_1
AM744818.1
Dviv_isotig19650
HBC04281_1
FD515431.1
XI03394
EX556154.1
CBC13439_1
OOC00359_1
MHC03469_1
CSC00377_1
HG04696
PTC02394_1
FC553904.1
Dviv_isotig24144
HGC11197_1
MHC02263_1
MI00285
FK803144.1
AS09900
Acan_isotig07670
FC555276.1
Name_isotig03923
ACC04183_1
HGC11643_1
HG04361
MI02034
Associated_featureWBsf655176
WBsf662790
WBsf1005274
WBsf1022956
WBsf235726
WBsf235727
WBsf235728
Experimental_infoRNAi_resultWBRNAi00041194Inferred_automaticallyRNAi_primary
Expr_patternExpr1024901
Expr1036877
Expr1145225
Expr2011080
Expr2029317
Drives_constructWBCnstr00028324
Construct_productWBCnstr00028324
Microarray_results (19)
Expression_cluster (191)
Interaction (64)
Map_infoMapXPosition-5.27561
PositivePositive_cloneC25F6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00013017
WBPaper00031988
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00056904
WBPaper00062388
WBPaper00065140
WBPaper00065331
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