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WormBase Tree Display for Gene: WBGene00021063

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Name Class

WBGene00021063SMapS_parentSequenceW06E11
IdentityVersion2
NameCGC_namesbds-1Person_evidenceWBPerson8131
Sequence_nameW06E11.4
Molecular_name (3)
Other_nameW06E11.cCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_W06E11.4Accession_evidenceNDBBX284603
Public_namesbds-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
204 Jun 2008 11:48:40WBPerson2970Name_changeCGC_namesbds-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsbds
Allele (41)
StrainWBStrain00051204
RNASeq_FPKM (74)
GO_annotation00077608
00077609
00077610
00077611
00077612
00077613
00077614
00077615
00125534
00125535
Contained_in_operonCEOP3028
Ortholog (36)
Structured_descriptionConcise_descriptionW06E11.4 encodes an ortholog of human SBDS (OMIM:607444, mutated in Shwachman-Bodian-Diamond syndrome) and S. cerevisiae Sdo1p, that is required for the extended lifespan of daf-2(e1370) mutants; W06E11.4 is expressed ubiquitously (or nearly so) in somatic larval and adult tissues; by orthology with yeast Sdo1p, W06E11.4 is predicted to be a nucleolar protein required for maturation of 60S ribosomal subunits; W06E11.4 shares an operon with tag-266 and T19C3.7.Paper_evidenceWBPaper00028829
WBPaper00028832
WBPaper00028833
WBPaper00028836
WBPaper00031212
WBPaper00032020
Curator_confirmedWBPerson567
Date_last_updated24 Jul 2008 00:00:00
Automated_descriptionPredicted to be involved in cytosolic ribosome assembly. Predicted to be located in cytoplasm; nuclear lumen; and spindle. Human ortholog(s) of this gene implicated in Shwachman-Diamond syndrome and aplastic anemia. Is an ortholog of human SBDS (SBDS ribosome maturation factor).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:12449Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19440)
DOID:0060479Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19440)
Molecular_infoCorresponding_CDSW06E11.4
Corresponding_transcriptW06E11.4.1
Other_sequenceAW626571.1
Tcol_isotig00942
PPC08400_1
AW257633.1
OVC00315_1
EX536428.1
Tcol_isotig00951
CJC00729_1
Oden_isotig06719
EY460479.1
NB06672
EY466003.1
OVC06529_1
JI223229.1
HCC10868_1
Dviv_isotig22373
PVC01524_1
Dviv_isotig22801
Dviv_isotig22374
EL889531.1
Oden_isotig06717
Tcol_isotig00941
Tcol_isotig00948
CV201145.1
PSC00269_1
Tcol_isotig00949
JI171533.1
Tcol_isotig00947
PPC06019_1
Tcol_isotig00944
FC540270.1
Oden_isotig06715
Oden_isotig29298
SR01570
HG02740
MIC00984_1
NBC00724_2
NB07099
Tcol_isotig00945
MI04072
SRC00573_1
AA618731.1
ACC05711_1
Hbac_isotig05540
GO249103.1
PPC02806_1
EX827810.1
Tcir_isotig20794
CR03858
Tcir_isotig14747
Tcir_isotig03393
FC542849.1
MI01547
Oden_isotig06716
ACC34831_1
BE638335.1
MIC07661_1
BE209053.1
HCC02975_1
EX555752.1
ACC05711_2
BMC08618_1
JI469667.1
ACC14369_1
FC809865.1
NBC00724_1
RS09961
EY466456.1
EY470474.1
Tcir_isotig03392
HGC03078_1
HO652385.1
CRC06021_1
RSC01893_1
MI08271
FC815221.1
Oden_isotig06718
EX536461.1
Oden_isotig06714
Tcol_isotig00950
HC02142
EY467662.1
CBC02010_1
AW208343.1
GW406002.1
Tcol_isotig00946
Tcol_isotig00943
BXC04172_1
BF727575.1
JI479848.1
Acan_isotig09016
Associated_featureWBsf226118
WBsf226119
Experimental_infoRNAi_result (12)
Expr_patternExpr1013363
Expr1039189
Expr1158436
Expr2015610
Expr2033845
Drives_constructWBCnstr00024700
Construct_productWBCnstr00024700
Microarray_results (19)
Expression_cluster (115)
Interaction (47)
Map_infoMapIIIPosition-26.4304Error0.009723
PositivePositive_cloneW06E11Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00030887
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