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WormBase Tree Display for Gene: WBGene00007194

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Name Class

WBGene00007194SMapS_parentSequenceB0491
IdentityVersion2
NameCGC_namedph-5Person_evidenceWBPerson3778
Sequence_nameB0491.7
Molecular_nameB0491.7
B0491.7.1
CE02109
Other_nameCELE_B0491.7Accession_evidenceNDBBX284602
Public_namedph-5
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:47WBPerson1971EventImportedInitial conversion from CDS class of WS125
211 Jun 2021 18:11:09WBPerson1983Name_changeCGC_namedph-5
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classdph
Allele (22)
RNASeq_FPKM (74)
GO_annotation00060454
00060455
00060456
00060457
00060458
00119427
00119428
00119429
Contained_in_operonCEOP2532
Ortholog (32)
Structured_descriptionConcise_descriptionB0491.7 encodes a putative diphthine synthase orthologous to S. cerevisiae DPH5; DPH5 is an S-adenosylmethionine:EF-2 methyltransferase required for the enzymatic conversion of 3-amino-3-carboxypropyl-histidine to diphthine; DPH5 adds at least the last two of the three methyl groups present in diphthine, and is homologous to bacterial AdoMet:uroporphyrinogen III methyltransferases.Paper_evidenceWBPaper00005654
WBPaper00012895
WBPaper00013419
WBPaper00013534
WBPaper00013537
WBPaper00013539
WBPaper00013556
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable diphthine methyl ester synthase activity and diphthine synthase activity. Predicted to be involved in methylation and protein histidyl modification to diphthamide. Human ortholog(s) of this gene implicated in neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties. Is an ortholog of human DPH5 (diphthamide biosynthesis 5).Paper_evidenceWBPaper00065943
WBPaper00067038
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS296 version of WormBase
Date_last_updated20 Mar 2025 00:00:00
Disease_infoPotential_modelDOID:0070479Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:24270)
Molecular_infoCorresponding_CDSB0491.7
Corresponding_transcriptB0491.7.1
Other_sequence (38)
Associated_featureWBsf989723
WBsf989724
WBsf1013217
WBsf1013218
WBsf222128
Experimental_infoRNAi_resultWBRNAi00061719Inferred_automaticallyRNAi_primary
WBRNAi00039105Inferred_automaticallyRNAi_primary
WBRNAi00009805Inferred_automaticallyRNAi_primary
WBRNAi00028169Inferred_automaticallyRNAi_primary
Expr_patternExpr1026360
Expr1033100
Expr1143263
Expr2000207
Expr2018427
Drives_constructWBCnstr00033929
Construct_productWBCnstr00033929
Microarray_results (20)
Expression_cluster (120)
SAGE_tagSAGE:aatgcagttggctgttgStrandSense
Unambiguously_mapped
SAGE:tcgacttccaStrandAntisense
SAGE:ttggaaactttcaggccStrandSense
Unambiguously_mapped
SAGE:ttggaaacttStrandSense
Unambiguously_mapped
Interaction (88)
Map_infoMapIIPosition3.45336
PositivePositive_cloneB0491Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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