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WormBase Tree Display for Gene: WBGene00017765

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Name Class

WBGene00017765SMapS_parentSequenceF25B4
IdentityVersion2
NameCGC_namegcst-1Person_evidenceWBPerson1997
Sequence_nameF25B4.1
Molecular_nameF25B4.1
F25B4.1.1
CE09620
Other_nameCELE_F25B4.1Accession_evidenceNDBBX284605
Public_namegcst-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:59WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
224 May 2012 16:35:53WBPerson2970Name_changeCGC_namegcst-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgcst
Allele (38)
StrainWBStrain00001589
WBStrain00002381
WBStrain00037899
RNASeq_FPKM (74)
GO_annotation00076858
00076859
00076860
00076861
00076862
00076863
00076864
00123078
00123079
Ortholog (35)
ParalogWBGene00010847Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009503Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013718Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015250Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00015251Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021355Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021564Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiongcst-1 is orthologous to the human gene GLYCINE CLEAVAGE SYSTEM T-PROTEIN (AMT; OMIM:238310), which when mutated leads to glycine encephalopathy.Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated06 Aug 2004 00:00:00
Automated_descriptionPredicted to enable aminomethyltransferase activity and transaminase activity. Predicted to be involved in glycine catabolic process. Predicted to be located in mitochondrion. Human ortholog(s) of this gene implicated in glycine encephalopathy. Is an ortholog of human AMT (aminomethyltransferase).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:9268Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:473)
Molecular_infoCorresponding_CDSF25B4.1
Corresponding_transcriptF25B4.1.1
Other_sequence (63)
Associated_featureWBsf646823
WBsf231790
WBsf231791
WBsf231792
WBsf231793
WBsf231794
Experimental_infoRNAi_resultWBRNAi00013845Inferred_automaticallyRNAi_primary
WBRNAi00113373Inferred_automaticallyRNAi_primary
WBRNAi00045465Inferred_automaticallyRNAi_primary
WBRNAi00106967Inferred_automaticallyRNAi_primary
WBRNAi00113372Inferred_automaticallyRNAi_primary
WBRNAi00033334Inferred_automaticallyRNAi_primary
Expr_patternChronogram211
Chronogram1570
Expr5844
Expr5845
Expr1028954
Expr1037629
Expr1149384
Expr2011975
Expr2030212
Drives_constructWBCnstr00002429
WBCnstr00004340
WBCnstr00027038
Construct_productWBCnstr00027038
Microarray_results (24)
Expression_cluster (134)
Interaction (106)
Map_infoMapVPosition-1.16141
PositivePositive_cloneF25B4Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00042204
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