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WormBase Tree Display for Gene: WBGene00010988

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Name Class

WBGene00010988SMapS_parentSequenceR03D7
IdentityVersion2
NameCGC_namemetr-1Person_evidenceWBPerson1711
Sequence_nameR03D7.1
Molecular_nameR03D7.1
R03D7.1.1
CE01609
Other_nameCELE_R03D7.1Accession_evidenceNDBBX284602
Public_namemetr-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:52WBPerson1971EventImportedInitial conversion from CDS class of WS125
220 Apr 2011 10:05:24WBPerson2970Name_changeCGC_namemetr-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmetr
Allele (55)
StrainWBStrain00001842
WBStrain00002165
WBStrain00031469
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (39)
ParalogWBGene00015512Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020491Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionmetr-1 encodes a protein orthologous to the human gene Methionine synthase (MTR), which is involved in the conversion of homocysteine to form methionine.Paper_evidenceWBPaper00042203
Curator_confirmedWBPerson324
WBPerson1823
WBPerson567
Date_last_updated07 May 2013 00:00:00
Automated_descriptionPredicted to enable methionine synthase activity. Predicted to be involved in homocysteine metabolic process; methionine biosynthetic process; and tetrahydrofolate metabolic process. Predicted to be located in cytosol. Used to study type 2 diabetes mellitus. Human ortholog(s) of this gene implicated in several diseases, including IgA glomerulonephritis; autistic disorder; and hematologic cancer (multiple). Is an ortholog of human MTR (5-methyltetrahydrofolate-homocysteine methyltransferase).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_infoExperimental_modelDOID:9352Homo sapiensPaper_evidenceWBPaper00042203
Curator_confirmedWBPerson324
Date_last_updated13 Mar 2023 00:00:00
Potential_model (14)
Models_disease_assertedWBDOannot00000175
Molecular_infoCorresponding_CDSR03D7.1
Corresponding_transcriptR03D7.1.1
Other_sequence (51)
Associated_featureWBsf222084
WBsf222085
Experimental_infoRNAi_resultWBRNAi00071221Inferred_automaticallyRNAi_primary
WBRNAi00034551Inferred_automaticallyRNAi_primary
WBRNAi00090587Inferred_automaticallyRNAi_primary
WBRNAi00051170Inferred_automaticallyRNAi_primary
WBRNAi00106971Inferred_automaticallyRNAi_primary
WBRNAi00017346Inferred_automaticallyRNAi_primary
Expr_patternChronogram417
Chronogram1093
Expr6447
Expr6448
Expr1028258
Expr1034818
Expr1154877
Expr2013538
Expr2031772
Drives_constructWBCnstr00002636
WBCnstr00004383
Regulate_expr_clusterWBPaper00060951:metr-1(os521)_downregulated
WBPaper00060951:metr-1(os521)_upregulated
Microarray_results (20)
Expression_cluster (213)
Interaction (110)
Map_infoMapIIPosition3.13342Error0.000132
PositivePositive_cloneR03D7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (25)
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