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WormBase Tree Display for Gene: WBGene00008775

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Name Class

WBGene00008775SMapS_parentSequenceF13H10
IdentityVersion2
NameCGC_namemogs-1Paper_evidenceWBPaper00042571
Sequence_nameF13H10.4
Molecular_nameF13H10.4a
F13H10.4a.1
CE40354
F13H10.4b
CE40355
F13H10.4c
CE40940
F13H10.4b.1
F13H10.4c.1
F13H10.4c.2
Other_nameagl-1Paper_evidenceWBPaper00042571
CELE_F13H10.4Accession_evidenceNDBBX284604
Public_namemogs-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:49WBPerson1971EventImportedInitial conversion from CDS class of WS125
220 May 2014 11:44:19WBPerson2970Name_changeCGC_namemogs-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmogs
Allele (56)
StrainWBStrain00036786
RNASeq_FPKM (74)
GO_annotation (15)
Contained_in_operonCEOP4400
Ortholog (39)
ParalogWBGene00019843Caenorhabditis elegansFrom_analysisPanther
Structured_descriptionConcise_descriptionmogs-1 encodes a mannosyl-oligosaccharide glucosidase (E.C. 3.2.1.106) orthologous to the human gene A-GLUCOSIDASE I (GCS1; OMIM:601336), which when mutated leads to disease.Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated20 May 2014 00:00:00
Automated_descriptionPredicted to enable Glc3Man9GlcNAc2 oligosaccharide glucosidase activity. Predicted to be involved in protein N-linked glycosylation. Predicted to be located in endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIb. Is an ortholog of human MOGS (mannosyl-oligosaccharide glucosidase).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:0070254Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:24862)
Molecular_infoCorresponding_CDSF13H10.4a
F13H10.4b
F13H10.4c
Corresponding_CDS_historyF13H10.4:wp162
Corresponding_transcriptF13H10.4a.1
F13H10.4b.1
F13H10.4c.1
F13H10.4c.2
Other_sequence (44)
Associated_featureWBsf652175
WBsf652177
WBsf652178
WBsf667645
WBsf668284
WBsf668285
WBsf668286
WBsf997751
WBsf230808
Experimental_infoRNAi_resultWBRNAi00076301Inferred_automaticallyRNAi_primary
WBRNAi00030910Inferred_automaticallyRNAi_primary
WBRNAi00112532Inferred_automaticallyRNAi_primary
WBRNAi00112531Inferred_automaticallyRNAi_primary
WBRNAi00044547Inferred_automaticallyRNAi_primary
WBRNAi00081637Inferred_automaticallyRNAi_primary
WBRNAi00112533Inferred_automaticallyRNAi_primary
WBRNAi00013242Inferred_automaticallyRNAi_primary
WBRNAi00025094Inferred_automaticallyRNAi_primary
WBRNAi00027277Inferred_automaticallyRNAi_primary
Expr_patternExpr1022953
Expr1033829
Expr1148501
Expr2013653
Expr2031887
Drives_constructWBCnstr00032698
Construct_productWBCnstr00032698
Microarray_results (27)
Expression_cluster (108)
Interaction (91)
Map_infoMapIVPosition4.78213
PositivePositive_cloneF13H10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029024
WBPaper00038491
WBPaper00042571
WBPaper00047713
WBPaper00051789
WBPaper00055090
WBPaper00062843
WBPaper00064403
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