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WormBase Tree Display for Gene: WBGene00006416

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Name Class

WBGene00006416EvidenceCGC_data_submission
SMapS_parentSequenceT13A10
IdentityVersion3
NameCGC_namesams-5Person_evidenceWBPerson1711
Sequence_nameT13A10.11
Molecular_nameT13A10.11a
T13A10.11a.1
CE30175
T13A10.11a.2
T13A10.11b
Other_nametag-32Person_evidenceWBPerson201
CELE_T13A10.11Accession_evidenceNDBBX284604
Public_namesams-5
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:40WBPerson1971EventImportedInitial conversion from geneace
228 May 2004 14:19:55WBPerson1971EventAcquires_mergeWBGene00020470
310 Sep 2008 16:37:04WBPerson2970Name_changeCGC_namesams-5
Other_nametag-32
Acquires_mergeWBGene00020470
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsams
Allele (80)
StrainWBStrain00035607
RNASeq_FPKM (74)
GO_annotation (14)
Ortholog (42)
ParalogWBGene00008205Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015538Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
WBGene00015540Caenorhabditis elegansFrom_analysisInparanoid_8
Panther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable methionine adenosyltransferase activity. Predicted to be involved in S-adenosylmethionine biosynthetic process. Predicted to be located in cytosol. Expressed in MI neuron. Human ortholog(s) of this gene implicated in hypermethioninemia and lung cancer. Is an ortholog of human MAT1A (methionine adenosyltransferase 1A) and MAT2A (methionine adenosyltransferase 2A).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:1324Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6904)
DOID:0050544Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6903)
Molecular_infoCorresponding_CDST13A10.11a
Corresponding_CDS_historyT13A10.11b:wp240
Corresponding_transcriptT13A10.11b
T13A10.11a.1
T13A10.11a.2
Other_sequence (99)
Associated_featureWBsf651841
WBsf1017500
WBsf230148
Experimental_infoRNAi_result (18)
Expr_patternChronogram39
Chronogram1065
Expr6686
Expr6687
Expr9881
Expr1013138
Expr1032605
Expr1156819
Expr2015589
Expr2033824
Drives_constructWBCnstr00003738
WBCnstr00003983
WBCnstr00007652
Regulate_expr_clusterWBPaper00065005:sams-5(RNAi)_downregulated
WBPaper00065005:sams-5(RNAi)_upregulated
Microarray_results (27)
Expression_cluster (254)
Interaction (108)
Map_infoMapIVPosition3.11769Error0.00136
PositivePositive_cloneT13A10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4509
Pseudo_map_position
ReferenceWBPaper00028451
WBPaper00038491
WBPaper00042204
WBPaper00055090
WBPaper00060612
WBPaper00061357
WBPaper00062291
WBPaper00063813
RemarkGene name created from parsing 'genotype' field from CGC strain informationCGC_data_submission
Map 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