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WormBase Tree Display for Gene: WBGene00000964

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Name Class

WBGene00000964EvidenceCGC_data_submission
SMapS_parentSequenceC47E12
IdentityVersion1
NameCGC_namedhp-2Person_evidenceWBPerson211
Sequence_nameC47E12.8
Molecular_nameC47E12.8
C47E12.8.1
CE05452
Other_nameCeCRMP/DHP-2Accession_evidenceEMBLAB040993
CELE_C47E12.8Accession_evidenceNDBBX284604
Public_namedhp-2
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:22WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdhp
AlleleWBVar01730526
WBVar01730527
WBVar01453815
WBVar01500079
WBVar01453816
WBVar01453817
WBVar01453818
WBVar01498996
WBVar01499925
WBVar02114941
WBVar01688082
WBVar00935103
WBVar00935104
WBVar00935105
WBVar00935106
WBVar00935107
WBVar00935108
WBVar00935109
WBVar00935110
WBVar00935111
WBVar00935112
WBVar00935113
WBVar00935114
WBVar00935115
WBVar00935116
WBVar00935117
WBVar00935118
WBVar01856507
WBVar02150414
WBVar01856508
WBVar00433200
WBVar00433201
WBVar00433202
WBVar00433203
WBVar00433204
WBVar00433205
WBVar00433206
WBVar02058567
WBVar01500245
Legacy_informationcommon ancestor of CRMP and dihydropyrimidinase [Takemoto et al via email13]
RNASeq_FPKM (74)
GO_annotation00061926
00061927
00061928
00061929
00061930
00061931
00061932
00061933
00061934
00061935
00061936
00061937
00061938
00108099
00108100
00108101
Ortholog (58)
ParalogWBGene00000963Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006769Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionThe dhp-2 gene encodes an ortholog of the human gene DIHYDROPYRIMIDINASE (DPYS), which when mutated leads to dihydropyrimidinuria (OMIM:222748).Paper_evidenceWBPaper00004637
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in cyclic amides. Involved in pyrimidine nucleobase catabolic process. Located in cytoplasm. Expressed in body wall musculature. Human ortholog(s) of this gene implicated in Ritscher-Schinzel syndrome; dihydropyrimidinase deficiency; and purine-pyrimidine metabolic disorder. Is an ortholog of human DPYS (dihydropyrimidinase).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:653Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3013)
DOID:0060565Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20637)
DOID:0111629Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:3013)
Molecular_infoCorresponding_CDSC47E12.8
Corresponding_transcriptC47E12.8.1
Other_sequence (50)
Associated_featureWBsf646270
WBsf997529
WBsf997530
WBsf1018033
WBsf228909
Experimental_infoRNAi_resultWBRNAi00042682Inferred_automaticallyRNAi_primary
WBRNAi00089011Inferred_automaticallyRNAi_primary
WBRNAi00012077Inferred_automaticallyRNAi_primary
WBRNAi00029914Inferred_automaticallyRNAi_primary
Expr_patternExpr835
Expr836
Expr1013617
Expr1030599
Expr1146671
Expr2010891
Expr2029130
Drives_constructWBCnstr00013281
WBCnstr00037174
Construct_productWBCnstr00013281
WBCnstr00037174
Microarray_results (21)
Expression_cluster (131)
Interaction (12)
Map_infoMapIVPosition4.4581Error0.000963
PositivePositive_cloneC47E12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004552
WBPaper00010035
WBPaper00023701
WBPaper00033099
WBPaper00038491
WBPaper00055090
WBPaper00065140
WBPaper00065331
RemarkSequence connection from [Kimura H]
Synonyms : ULIP-A, CeCRMP/DHP-2
Map 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