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WormBase Tree Display for Gene: WBGene00010941

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Name Class

WBGene00010941SMapS_parentSequenceM176
IdentityVersion2
NameCGC_namegss-1Person_evidenceWBPerson3046
Sequence_nameM176.2
Molecular_nameM176.2
M176.2.1
CE18087
Other_nameCELE_M176.2Accession_evidenceNDBBX284602
Public_namegss-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:52WBPerson1971EventImportedInitial conversion from CDS class of WS125
218 Mar 2011 16:31:15WBPerson2970Name_changeCGC_namegss-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgss
Allele (30)
StrainWBStrain00001901
WBStrain00001902
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (40)
Structured_descriptionConcise_descriptiongss-1 encodes the C. elegans ortholog of glutathione synthetase (GSS; OMIM:601002), which when mutated leads to 5-oxoprolinuria, or to GSS deficiency restricted to erythrocytes and associated only with hemolytic anemia; GSS-1 is predicted to catalyze the second step of glutathione (GSH) biosynthesis in which the dipeptide c-Glu-Cys is conjugated with glycine.Paper_evidenceWBPaper00004637
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated10 Dec 2014 00:00:00
Automated_descriptionPredicted to enable glutathione binding activity and glutathione synthase activity. Predicted to be involved in glutathione biosynthetic process. Predicted to be located in cytosol. Expressed in head. Human ortholog(s) of this gene implicated in Alzheimer's disease; glutathione synthetase deficiency of erythrocytes; and glutatione synthetase deficiency with 5-oxoprolinuria. Is an ortholog of human GSS (glutathione synthetase).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:4624)
DOID:0080699Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4624)
DOID:0081034Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4624)
DOID:0112252Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4624)
Molecular_infoCorresponding_CDSM176.2
Corresponding_transcriptM176.2.1
Other_sequence (25)
Associated_featureWBsf019117
WBsf019118
WBsf019119
WBsf019120
WBsf655382
WBsf223647
Experimental_infoRNAi_resultWBRNAi00025998Inferred_automaticallyRNAi_primary
WBRNAi00115452Inferred_automaticallyRNAi_primary
WBRNAi00009015Inferred_automaticallyRNAi_primary
WBRNAi00033513Inferred_automaticallyRNAi_primary
WBRNAi00115518Inferred_automaticallyRNAi_primary
WBRNAi00050997Inferred_automaticallyRNAi_primary
Expr_patternChronogram1317
Expr6428
Expr6429
Expr6430
Expr1024814
Expr1034802
Expr1154705
Expr2012292
Expr2030528
Drives_constructWBCnstr00002692
WBCnstr00002693
WBCnstr00004395
WBCnstr00031040
Construct_productWBCnstr00031040
Microarray_results (20)
Expression_cluster (113)
Interaction (71)
Map_infoMapIIPosition1.39871Error0.004281
PositivePositive_cloneM176Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00006024
WBPaper00038491
WBPaper00045711
WBPaper00048470
WBPaper00055090
WBPaper00059495
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