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WormBase Tree Display for Gene: WBGene00007836

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Name Class

WBGene00007836SMapS_parentSequenceC31C9
IdentityVersion2
NameCGC_namephdh-1Person_evidenceWBPerson555
Sequence_nameC31C9.2
Molecular_nameC31C9.2a
C31C9.2a.1
CE08497
C31C9.2b
CE54570
C31C9.2b.1
Other_nameCELE_C31C9.2Accession_evidenceNDBBX284602
Public_namephdh-1
DB_infoDatabaseAceViewgene2N928
WormQTLgeneWBGene00007836
WormFluxgeneWBGene00007836
NDBlocus_tagCELE_C31C9.2
PanthergeneCAEEL|WormBase=WBGene00007836|UniProtKB=O17626
familyPTHR42938
NCBIgene175012
RefSeqproteinNM_001421351.1
NM_064467.6
TrEMBLUniProtAccO17626
UniProt_GCRPUniProtAccO17626
OMIMgene606879
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
205 May 2023 12:43:53WBPerson51134Name_changeCGC_namephdh-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classphdh
Allele (40)
StrainWBStrain00002470
WBStrain00002285
RNASeq_FPKM (74)
GO_annotation00030184
00030185
00115863
00115864
Ortholog (37)
ParalogWBGene00006424Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionC31C9.2 is orthologous to the human gene PHOSPHOGLYCERATE DEHYDROGENASE (PHGDH; OMIM:606879), which when mutated leads to phosphoglycerate dehydrogenase deficiency.Paper_evidenceWBPaper00004637
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable phosphoglycerate dehydrogenase activity. Human ortholog(s) of this gene implicated in Neu-Laxova syndrome 1 and PHGDH deficiency. Is an ortholog of human PHGDH (phosphoglycerate 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_modelDOID:0050722Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8923)
DOID:0080076Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8923)
DOID:9252Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8923)
Molecular_infoCorresponding_CDSC31C9.2a
C31C9.2b
Corresponding_transcriptC31C9.2a.1
C31C9.2b.1
Other_sequence (102)
Associated_featureWBsf650701
WBsf666326
WBsf666327
WBsf990477
WBsf1013672
WBsf224201
WBsf224202
WBsf224203
Experimental_infoRNAi_resultWBRNAi00000446Inferred_automaticallyRNAi_primary
WBRNAi00041604Inferred_automaticallyRNAi_primary
WBRNAi00029382Inferred_automaticallyRNAi_primary
WBRNAi00022541Inferred_automaticallyRNAi_primary
WBRNAi00011432Inferred_automaticallyRNAi_primary
Expr_patternChronogram1157
Chronogram1714
Expr5396
Expr5397
Expr1013361
Expr1033396
Expr1145629
Expr2001274
Expr2019496
Drives_constructWBCnstr00002985
WBCnstr00004485
WBCnstr00033446
Construct_productWBCnstr00033446
Microarray_results (22)
Expression_cluster (241)
Interaction (78)
Map_infoMapIIPosition18.9113
PositivePositive_cloneC31C9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
WBPaper00056038
WBPaper00062642
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