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WormBase Tree Display for Gene: WBGene00014095

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Name Class

WBGene00014095SMapS_parentSequenceZK829
IdentityVersion2
NameCGC_namegdh-1Paper_evidenceWBPaper21864529
Sequence_nameZK829.4
Molecular_nameZK829.4
ZK829.4.1
CE06652
ZK829.4.2
Other_nameCELE_ZK829.4Accession_evidenceNDBBX284604
Public_namegdh-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:55WBPerson1971EventImportedInitial conversion from CDS class of WS125
231 Aug 2011 09:11:34WBPerson2970Name_changeCGC_namegdh-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgdh
Allele (37)
StrainWBStrain00001547
WBStrain00002442
WBStrain00055460
RNASeq_FPKM (74)
GO_annotation00079104
00079105
00079106
00079107
00079108
00079109
00120823
00120824
00120825
Ortholog (46)
ParalogWBGene00045131Caenorhabditis elegansFrom_analysismodENCODE_Pseudogenes
Structured_descriptionConcise_descriptiongdh-1 encodes a glutamate dehydrogenase, required in mass RNAi assays for normal fertility and rapid growth, that is expressed in larval and adult pharynx, intestine, and rectal gland cells; GDH-1 is orthologous to human GLUD1 (OMIM:138130, mutated in hyperinsulinemic hypoglycemia and hyperammonemia) and GLUD2 (OMIM:300144).Paper_evidenceWBPaper00006525
WBPaper00024497
WBPaper00029258
WBPaper00031006
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated20 Sep 2011 00:00:00
Automated_descriptionPredicted to enable glutamate dehydrogenase (NAD+) activity. Predicted to be involved in glutamate catabolic process. Predicted to be located in mitochondrion. Expressed in head; intestine; pharynx; rectal gland cell; and tail. Human ortholog(s) of this gene implicated in Alzheimer's disease; glucose metabolism disease (multiple); and late onset Parkinson's disease. Is an ortholog of human GLUD1 (glutamate dehydrogenase 1).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4335)
DOID:9993Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4335)
DOID:0070217Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4335)
DOID:2018Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4335)
Molecular_infoCorresponding_CDSZK829.4
Corresponding_transcriptZK829.4.1
ZK829.4.2
Other_sequence (403)
Associated_feature (13)
Experimental_infoRNAi_result (17)
Expr_patternChronogram204
Expr7259
Expr7260
Expr14639
Expr1013000
Expr1036313
Expr1163175
Expr2012006
Expr2030242
Drives_constructWBCnstr00002389
WBCnstr00029313
WBCnstr00041190
Construct_productWBCnstr00016475
WBCnstr00029313
WBCnstr00041190
Microarray_results (26)
Expression_cluster (222)
Interaction (153)
Map_infoMapIVPosition5.45243Error0.000619
PositivePositive_cloneZK829Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00033090
WBPaper00038491
WBPaper00041022
WBPaper00042178
WBPaper00049595
WBPaper00055090
WBPaper00059575
WBPaper00061178
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