Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00004483

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00004483SMapS_parentSequenceF37C12
IdentityVersion1
NameCGC_namerps-14
Sequence_nameF37C12.9
Molecular_nameF37C12.9
F37C12.9.1
CE00821
Other_nameCELE_F37C12.9Accession_evidenceNDBBX284603
Public_namerps-14
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:35WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classrps
Allele (15)
Legacy_informationOrthologous to yeast (S.cerevisiae) ribosomal protein rps14 using blastP
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (39)
ParalogWBGene00012244Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionrps-14 encodes a small ribosomal subunit S14 protein; by homology, RPS-14 is predicted to function in protein biosynthesis; in C. elegans, RPS-14 activity is required for embryonic and germline development, as well as the overall health of the animal; RPS-14 co-immuoprecipitates with ALG-1, a C. elegans Argonaut ortholog.Paper_evidenceWBPaper00004403
WBPaper00005654
WBPaper00034755
Curator_confirmedWBPerson1843
Date_last_updated03 Sep 2012 00:00:00
Automated_descriptionPredicted to be a structural constituent of ribosome. Predicted to be involved in ribosomal small subunit assembly and translation. Predicted to be located in cytoplasm; nucleolus; and ribosome. Predicted to be part of cytosolic small ribosomal subunit and small-subunit processome. Expressed in tail. Human ortholog(s) of this gene implicated in chromosome 5q deletion syndrome. Is an ortholog of human RPS14 (ribosomal protein S14).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:0090016Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10387)
Molecular_infoCorresponding_CDSF37C12.9
Corresponding_transcriptF37C12.9.1
Other_sequence (333)
Associated_featureWBsf651179
WBsf667044
WBsf667045
WBsf226924
Experimental_infoRNAi_result (28)
Expr_patternExpr5983
Expr1015336
Expr1032286
Expr1150501
Expr2015508
Expr2033743
Drives_constructWBCnstr00002450
WBCnstr00035450
Construct_productWBCnstr00035450
Microarray_results (21)
Expression_cluster (175)
Interaction (238)
Map_infoMapIIIPosition-0.776434Error0.00013
PositivePositive_cloneF37C12Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00005356
WBPaper00028564
WBPaper00034755
WBPaper00035149
WBPaper00035215
WBPaper00038491
WBPaper00049828
WBPaper00055090
WBPaper00060474
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