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WormBase Tree Display for Gene: WBGene00004421

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Name Class

WBGene00004421EvidenceAccession_evidenceEMBLAJ270980
SMapS_parentSequenceF10B5
IdentityVersion1
NameCGC_namerpl-10
Sequence_nameF10B5.1
Molecular_nameF10B5.1
F10B5.1.1
CE01543
Other_nameCELE_F10B5.1Accession_evidenceNDBBX284602
Public_namerpl-10
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrpl
Allele (14)
Legacy_informationOrthologous to yeast (S.cerevisiae) ribosomal protein rpl10 using blastP
StrainWBStrain00047649
RNASeq_FPKM (74)
GO_annotation00054607
00054608
00054609
00054610
00112824
00112825
00112826
Contained_in_operonCEOP2340
Ortholog (43)
Structured_descriptionConcise_descriptionrpl-10 encodes a large ribosomal subunit L10 protein required in mass RNAi assays for embryonic viability, fertility, normally rapid growth, and normal body coloration; the rpl-10 transcription unit has a nonsense transcript that is up-regulated in vivo by smg[-] mutations, indicating that rpl-10 is a natural substrate for SMG-mediated nonsense suppresssion; several other natural mRNA substrates of SMG suppression (e.g., rpl-3, rpl-7, rpl-12) have protein products that are involved in translation.Paper_evidenceWBPaper00004313
WBPaper00004540
WBPaper00004651
WBPaper00005654
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be a structural constituent of ribosome. Predicted to be involved in translation. Predicted to be located in ribosome. Predicted to be part of cytosolic large ribosomal subunit. Expressed in head; pharyngeal muscle cell; and tail. Human ortholog(s) of this gene implicated in autistic disorder; spermatogenic failure 63; and syndromic X-linked mental retardation 35. Is an ortholog of human RPL10 (ribosomal protein L10) and RPL10L (ribosomal protein L10 like).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:0112356Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17976)
DOID:12849Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10298)
DOID:0080241Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10298)
Molecular_infoCorresponding_CDSF10B5.1
Corresponding_transcriptF10B5.1.1
Other_sequence (421)
Associated_featureWBsf644443
WBsf654899
WBsf657205
WBsf657943
WBsf657944
WBsf221692
WBsf221693
Experimental_infoRNAi_result (19)
Expr_patternChronogram624
Expr98
Expr5711
Expr1019983
Expr1032225
Expr1148166
Expr2015437
Expr2033672
Drives_constructWBCnstr00002441
WBCnstr00035500
Construct_productWBCnstr00035500
Microarray_results (26)
Expression_cluster (171)
Interaction (260)
Map_infoMapIIPosition0.711423Error0.00128
PositivePositive_cloneF10B5Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00004313
WBPaper00025088
WBPaper00030791
WBPaper00035149
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00060235
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