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_name (3)
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_sequenceASC25887_1
Acan_isotig19951
FE914405.1
GQ422281.1
RSC00154_1
CB043385.1
EF634885.1
BI772982.1
FC821494.1
HGC08058_1
SSC03947_1
BI773110.1
Tcir_isotig16704
TS00889
BMC12236_1
PTC03177_1
FE914881.1
EF634878.1
BU087129.1
AE01182
FE915007.1
AI574575.1
Tcir_isotig01807
PT00976
GR11850
ES560752.1
FE916331.1
EF634884.1
CK850434.1
GT571273.1
NAC00561_1
ES740524.1
BMC12237_2
PSC02039_2
EX915014.1
EX009834.1
HC01599
HG09742
ALC00862_1
MC01100
BI772841.1
GO250027.1
Oden_isotig21609
EX008511.1
AS02875
BE491934.1
EY465288.1
PT03941
PT00010
PPC05200_1
SSC06236_1
GR367646.1
Tcir_isotig01809
EF634880.1
AS07727
GPC00453_1
PT00597
EF634875.1
MIC01058_1
RS05848
GO248888.1
PT00051
NBC00684_1
BE125008.1
BI772818.1
BI773153.1
NB07570
FC820858.1
Name_isotig03424
GQ422282.1
MHC08400_1
CBC05768_1
CR08989
DIC01461_1
AI374036.1
HGC01808_1
EF634888.1
ES880213.1
FE917415.1
AA901493.1
FG619299.1
TM00853
FE913881.1
AW739463.1
HC04739
GQ422273.1
GO252455.1
ACC06113_1
CR09018
CB043177.1
ES880469.1
Dviv_isotig18361
ES742135.1
FC821833.1
EF634887.1
TX00271
GT570781.1
FE918981.1
MJC00131_1
GQ422280.1
EF634879.1
GO239416.1
GW407038.1
Dviv_isotig18360
HC02261
FE911266.1
CBC09161_1
AS17399
AS14889
FC821584.1
GO249752.1
PT04155
GQ422269.1
AA917279.1
Acan_isotig14917
TDC00060_1
AS13072
DI02528
EF634881.1
BI772944.1
ES740257.1
BI773083.1
OOC03335_1
Tcir_isotig01810
GR979172.1
XIC00602_1
TSC00853_1
GQ422279.1
EF634877.1
SS01392
XI01142
Tcol_isotig20295
EX500478.1
CBC00467_2
HG11595
MJ00733
BXC00289_1
EF634889.1
HS01577
EF634882.1
PTC03675_1
WBC00982_1
BI772977.1
FE919861.1
MH10512
AS03055
CJC00217_1
GQ422270.1
ES563976.1
FC821223.1
DI02536
HSC01628_1
Name_isotig07680
MI02358
AYC04593_2
PPC00135_1
NBC08666_1
HCC00643_2
BI773198.1
CK855136.1
SRC07744_1
CK850667.1
MPC00500_1
GRC00846_1
MCC03422_1
GR12399
SC01484
BI773096.1
TSC15045_1
FE918511.1
FE908512.1
GE625861.1
HG11905
HG06361
EX012641.1
FE920144.1
SSC02531_1
RSC00353_1
HS01585
EX010461.1
HBC10165_1
Tcir_isotig17600
PVC00863_1
DAC01393_1
BI773175.1
Hbac_isotig05566
RS09452
HG12298
HGC00666_1
FE917176.1
FC816548.1
NB07691
GP00119
HCC09297_1
Tcir_isotig24772
ACC01421_1
TCC00410_1
DA04110
MI00607
GW410400.1
EX008723.1
GT571275.1
AS07676
DVC02092_1
FC820955.1
GQ422278.1
BU086545.1
BI772856.1
SSC02524_1
ES740750.1
FC810074.1
EF634876.1
BI772936.1
JI464282.1
BU088394.1
DI02049
BI772870.1
FC820880.1
BU088932.1
BM965253.1
CSC01767_1
EF634886.1
SR01003
Tcol_isotig23504
GE638432.1
HBC00555_1
EF634890.1
CK850535.1
HG10951
FE914376.1
EX915610.1
HG11431
AS16773
BI772875.1
BI773199.1
BI773194.1
BMC00207_3
CV200000.1
OVC01395_1
HCC00643_1
BI773148.1
AI111242.1
BU586774.1
CJC04953_1
BE720999.1
EX009613.1
GQ422274.1
GQ422271.1
TS03076
PP00595
CB043751.1
HGC05541_1
EF634883.1
MJ01320
FE918200.1
PTC02963_1
AE01062
CR02701
JI214047.1
TMC00525_1
GQ422276.1
Tcir_isotig20920
DI02085
ES566116.1
FE917762.1
EV850903.1
BI772991.1
GR367613.1
FC815443.1
DI00385
HC04875
FC811073.1
GR367611.1
JI221081.1
GQ422277.1
BI773054.1
CBC02482_1
BG467848.1
BI773055.1
RS08895
CRC06347_1
CRC00114_1
GR367769.1
MP00464
HG09910
CD455421.1
BMC12237_1
FE915670.1
AI368343.1
BI772993.1
SRC00083_1
AI815324.1
GO251812.1
HG03506
Tcol_isotig18022
FE919204.1
AYC04593_1
NBC06011_1
FD517050.1
BU087219.1
GO251359.1
TSC09772_1
ES568668.1
JI250164.1
BM965350.1
ASC17430_1
EF634891.1
GQ422272.1
Acan_isotig10463
BU087403.1
ES743654.1
EF634874.1
BI772888.1
FE912737.1
PT00759
FC821511.1
BI773131.1
DI02526
CJC05268_1
HG10785
PTC01870_1
FE913989.1
HG09908
AS12075
FE906456.1
HGC02083_1
GQ422283.1
AS01405
CR11310
Tcir_isotig01808
Acan_isotig22052
HS01573
GQ422275.1
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