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WormBase Tree Display for Gene: WBGene00045383

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Name Class

WBGene00045383SMapS_parentSequenceC25A1
IdentityVersion2
NameCGC_namesup-46Paper_evidenceWBPaper00028588
Person_evidenceWBPerson261
Sequence_nameC25A1.4
Molecular_nameC25A1.4
C25A1.4.1
CE08369
Other_nameCELE_C25A1.4Accession_evidenceNDBBX284601
Public_namesup-46
DB_infoDatabaseNDBlocus_tagCELE_C25A1.4
PanthergeneCAEEL|WormBase=WBGene00045383|UniProtKB=Q9XVS2
familyPTHR23003
NCBIgene172881
RefSeqproteinNM_060276.6
TREEFAMTREEFAM_IDTF313406
TrEMBLUniProtAccQ9XVS2
UniProt_GCRPUniProtAccQ9XVS2
SpeciesCaenorhabditis elegans
HistoryVersion_change112 Apr 2007 13:43:01WBPerson2970EventCreated
201 Aug 2017 12:21:15WBPerson2970EventAcquires_mergeWBGene00007706
Name_changeSequence_nameC25A1.4
Acquires_mergeWBGene00007706
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsup
Allele (35)
StrainWBStrain00040607
WBStrain00040604
WBStrain00040606
WBStrain00005633
WBStrain00005630
WBStrain00051098
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (43)
Structured_descriptionConcise_descriptionsup-46, when mutated, suppresses the lethality of gna-2(qa705); however, the three suppressor alleles (qa707, qa708, qa709) require a gna-1(+) background for suppression, suggesting that uridine diphosphate-N-acetylglucosamine (UDP-GlcNAc) synthesis is indispensable for embryonic development, and that SUP-46 normally inhibits GNA-1 in tissues where GNA-2 is normally active.Paper_evidenceWBPaper00028588
Curator_confirmedWBPerson567
Date_last_updated20 Jul 2017 00:00:00
Automated_descriptionPredicted to enable mRNA binding activity. Predicted to be located in cytoplasm and nucleus. Expressed in germ cell and somatic cell. Human ortholog(s) of this gene implicated in colorectal carcinoma and leiomyoma. Is an ortholog of human HNRNPM (heterogeneous nuclear ribonucleoprotein M) and MYEF2 (myelin expression factor 2).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:127Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5046)
DOID:0080199Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5046)
Molecular_info (4)
Experimental_infoRNAi_resultWBRNAi00082502Inferred_automaticallyRNAi_primary
WBRNAi00082575Inferred_automaticallyRNAi_primary
WBRNAi00061737Inferred_automaticallyRNAi_primary
WBRNAi00102167Inferred_automaticallyRNAi_primary
WBRNAi00029172Inferred_automaticallyRNAi_primary
WBRNAi00116904Inferred_automaticallyRNAi_primary
WBRNAi00041144Inferred_automaticallyRNAi_primary
WBRNAi00003012Inferred_automaticallyRNAi_primary
Expr_patternExpr15106
Expr1020053
Expr1033335
Expr1145177
Expr2001062
Expr2019281
Drives_constructWBCnstr00033542
Construct_productWBCnstr00033542
Microarray_results (23)
Expression_cluster (123)
InteractionWBInteraction000050763
WBInteraction000505776
WBInteraction000505777
WBInteraction000509968
WBInteraction000509971
WBInteraction000509972
WBInteraction000509977
WBInteraction000509978
WBInteraction000509983
WBInteraction000509987
WBInteraction000509990
WBInteraction000509991
WBInteraction000509992
WBInteraction000516037
WBInteraction000516042
WBInteraction000543366
WBInteraction000547335
WBInteraction000547355
WBInteraction000547356
WBInteraction000547357
WBInteraction000547358
WBInteraction000547359
WBInteraction000547360
WBInteraction000547361
WBInteraction000547362
WBInteraction000547363
WBInteraction000547364
WBInteraction000552124
WBInteraction000553310
WBInteraction000557825
WBInteraction000559083
WBInteraction000560617
WBInteraction000564793
WBInteraction000564903
WBInteraction000569739
WBInteraction000570088
WBInteraction000574799
WBInteraction000583574
Map_infoMapIPosition4.71731
PositivePositive_cloneC25A1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00051515
WBPaper00055090
WBPaper00064339
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