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WormBase Tree Display for Gene: WBGene00018877

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Name Class

WBGene00018877SMapS_parentSequenceF55D10
IdentityVersion2
NameCGC_nameaman-1Paper_evidenceWBPaper00027768
Sequence_nameF55D10.1
Molecular_nameF55D10.1
F55D10.1.1
CE28456
Other_nameCELE_F55D10.1Accession_evidenceNDBBX284606
Public_nameaman-1
DB_infoDatabase (13)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:00WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
205 Jan 2007 17:07:18WBPerson1847Name_changeCGC_nameaman-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classaman
Allele (87)
StrainWBStrain00001773
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (46)
ParalogWBGene00010284Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018594Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionaman-1 encodes an ortholog of human lysosomal mannosidase (MAN2B1;OMIM:609458, mutated in alpha-mannosidosis); AMAN-1 is predicted to helpdigest glycoproteins by removing mannose residues from their N-linkedoligosaccharides; AMAN-1 has seven predicted N-glycosylation sites;AMAN-1 is biochemically active in vitro, has optimal activity at pH4-4.5, and is unaffected by Co(II); however, AMAN-1 expressed in Pichiapastoris lacks normal activity, perhaps because it requires othersubunits in vivo; aman-1 is expressed in neurons and intestine.Paper_evidenceWBPaper00006525
WBPaper00027768
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated14 Mar 2007 00:00:00
Automated_descriptionPredicted to enable alpha-mannosidase activity. Predicted to be involved in mannose metabolic process. Predicted to be located in lysosome. Human ortholog(s) of this gene implicated in alpha-mannosidosis. Is an ortholog of human MAN2B1 (mannosidase alpha class 2B member 1).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:3413Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6826)
Molecular_infoCorresponding_CDSF55D10.1
Corresponding_transcriptF55D10.1.1
Other_sequence (44)
Associated_featureWBsf648039
WBsf662713
WBsf1005046
WBsf1005047
WBsf1005048
WBsf1022842
WBsf235625
Experimental_infoRNAi_resultWBRNAi00015725Inferred_automaticallyRNAi_primary
WBRNAi00076484Inferred_automaticallyRNAi_primary
WBRNAi00048493Inferred_automaticallyRNAi_primary
WBRNAi00081081Inferred_automaticallyRNAi_primary
Expr_patternChronogram257
Expr6204
Expr1011721
Expr1038146
Expr1152284
Expr2009320
Expr2027556
Drives_constructWBCnstr00002587
WBCnstr00026220
Construct_productWBCnstr00009554
WBCnstr00026220
Microarray_results (20)
Expression_cluster (176)
InteractionWBInteraction000049245
WBInteraction000253230
WBInteraction000371124
WBInteraction000463533
WBInteraction000573870
Map_infoMapXPosition-6.75069
PositivePositive_cloneF55D10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027768
WBPaper00029024
WBPaper00034662
WBPaper00038491
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