RPS3A (ribosomal protein S3A) - Rat Genome Database

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Gene: RPS3A (ribosomal protein S3A) Homo sapiens
Analyze
Symbol: RPS3A
Name: ribosomal protein S3A
RGD ID: 1348881
HGNC Page HGNC:10421
Description: Enables mRNA 5'-UTR binding activity. A structural constituent of ribosome. Involved in negative regulation of apoptotic process; ribosomal small subunit biogenesis; and translation. Located in cytosol; endoplasmic reticulum; and nucleolus. Part of cytosolic small ribosomal subunit and small-subunit processome.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 40S ribosomal protein S3a; eS1; fte-1; FTE1; MFTL; MGC23240; S3A; small ribosomal subunit protein eS1; v-fos transformation effector protein 1
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Alliance Genes
More Info more info ...
Related Pseudogenes: AC073648.2   LOC100419321   LOC100419525   LOC100419565   RPS3AP1   RPS3AP10   RPS3AP11   RPS3AP12   RPS3AP13   RPS3AP14   RPS3AP15   RPS3AP16   RPS3AP17   RPS3AP18   RPS3AP19   RPS3AP2   RPS3AP20   RPS3AP21   RPS3AP22   RPS3AP23   RPS3AP24   RPS3AP25   RPS3AP26   RPS3AP27   RPS3AP28   RPS3AP29   RPS3AP3   RPS3AP30   RPS3AP31   RPS3AP32   RPS3AP33   RPS3AP34   RPS3AP35   RPS3AP36   RPS3AP37   RPS3AP38   RPS3AP39   RPS3AP4   RPS3AP40   RPS3AP41   RPS3AP42   RPS3AP43   RPS3AP44   RPS3AP46   RPS3AP47   RPS3AP48   RPS3AP49   RPS3AP5   RPS3AP50   RPS3AP51   RPS3AP52   RPS3AP53   RPS3AP54   RPS3AP55   RPS3AP6   RPS3AP7   RPS3AP8   RPS3AP9  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh384151,099,628 - 151,104,642 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl4151,099,624 - 151,104,642 (+)EnsemblGRCh38hg38GRCh38
GRCh374152,020,780 - 152,025,794 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 364152,240,204 - 152,245,254 (+)NCBINCBI36Build 36hg18NCBI36
Build 344152,378,388 - 152,383,393NCBI
Celera4149,342,420 - 149,347,475 (+)NCBICelera
Cytogenetic Map4q31.3NCBI
HuRef4147,746,045 - 147,751,132 (+)NCBIHuRef
CHM1_14151,997,753 - 152,002,834 (+)NCBICHM1_1
T2T-CHM13v2.04154,423,512 - 154,428,526 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(-)-epigallocatechin 3-gallate  (EXP)
1,2-dichloroethane  (ISO)
1,2-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (EXP)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,4,6-tribromophenol  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (EXP,ISO)
5-methoxy-2-\{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl\}-1H-benzimidazole  (ISO)
6-propyl-2-thiouracil  (ISO)
acrolein  (EXP)
aflatoxin B1  (EXP)
amiodarone  (ISO)
ammonium chloride  (ISO)
Aroclor 1254  (ISO)
arsenite(3-)  (EXP)
benzbromarone  (ISO)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (EXP,ISO)
bleomycin A2  (ISO)
bromobenzene  (ISO)
cadmium atom  (EXP,ISO)
cadmium dichloride  (EXP,ISO)
caffeine  (EXP)
calcium atom  (ISO)
calcium(0)  (ISO)
CGP 52608  (EXP)
chloropicrin  (EXP)
chlorpyrifos  (ISO)
chromium(6+)  (EXP,ISO)
cisplatin  (EXP)
clofibrate  (ISO)
clofibric acid  (ISO)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) sulfate  (EXP)
coumarin  (EXP)
cylindrospermopsin  (ISO)
decabromodiphenyl ether  (EXP)
dicrotophos  (EXP)
diethylstilbestrol  (EXP)
dioxygen  (ISO)
disodium selenite  (EXP)
enzyme inhibitor  (EXP)
epoxiconazole  (ISO)
ethanol  (ISO)
fenbuconazole  (EXP)
flutamide  (ISO)
folic acid  (ISO)
FR900359  (EXP)
genistein  (ISO)
hydrogen peroxide  (EXP)
isoprenaline  (ISO)
ivermectin  (EXP)
L-ethionine  (ISO)
lipopolysaccharide  (EXP)
methoxychlor  (ISO)
mitomycin C  (EXP)
N-nitrosodiethylamine  (ISO)
nickel subsulfide  (EXP)
nimesulide  (ISO)
nitrofen  (ISO)
nitroglycerin  (ISO)
omeprazole  (ISO)
ozone  (EXP)
p-menthan-3-ol  (EXP)
paracetamol  (EXP,ISO)
perfluorooctanoic acid  (EXP)
phenethyl caffeate  (ISO)
PhIP  (ISO)
pirinixic acid  (ISO)
potassium chromate  (EXP)
Propiverine  (ISO)
resveratrol  (EXP,ISO)
SB 431542  (EXP)
sodium arsenite  (EXP)
sodium dichromate  (EXP)
sodium fluoride  (ISO)
thioacetamide  (ISO)
trichloroethene  (ISO)
valproic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytoplasm  (HDA,IDA,IEA,NAS)
cytosol  (IBA,IDA,IEA,ISS,TAS)
cytosolic ribosome  (IDA)
cytosolic small ribosomal subunit  (HDA,IDA,IEA,ISO,NAS)
endoplasmic reticulum  (IDA)
extracellular exosome  (HDA)
focal adhesion  (HDA)
nucleolus  (HDA,IDA,IEA)
nucleoplasm  (TAS)
nucleus  (HDA,IEA,ISS)
ribonucleoprotein complex  (IDA,IEA)
ribosome  (IEA)
small ribosomal subunit  (ISO)
small-subunit processome  (IDA)
synapse  (IEA,ISO)

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Structures of the human and Drosophila 80S ribosome. Anger AM, etal., Nature. 2013 May 2;497(7447):80-5. doi: 10.1038/nature12104.
2. Functional dichotomy of ribosomal proteins during the synthesis of mammalian 40S ribosomal subunits. O'Donohue MF, etal., J Cell Biol. 2010 Sep 6;190(5):853-66. doi: 10.1083/jcb.201005117.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1398113   PMID:7821789   PMID:8076819   PMID:8647443   PMID:8706699   PMID:8722009   PMID:8877097   PMID:9566973   PMID:9573378   PMID:9582194   PMID:10713066   PMID:11790116  
PMID:11790298   PMID:11823430   PMID:12463423   PMID:12477932   PMID:12588972   PMID:12690205   PMID:12882984   PMID:14499622   PMID:15047060   PMID:15146197   PMID:15189156   PMID:15231748  
PMID:15303970   PMID:15489334   PMID:15572026   PMID:15592455   PMID:15883184   PMID:15889794   PMID:16055720   PMID:16159877   PMID:16169070   PMID:16213212   PMID:16263121   PMID:16385451  
PMID:16791210   PMID:16964243   PMID:17081983   PMID:17267499   PMID:17289661   PMID:17353931   PMID:17361185   PMID:17461779   PMID:17620599   PMID:18247557   PMID:18457437   PMID:18809582  
PMID:19019082   PMID:19596686   PMID:19738201   PMID:19805454   PMID:20020773   PMID:20458337   PMID:20686565   PMID:21081503   PMID:21081666   PMID:21145461   PMID:21182205   PMID:21280222  
PMID:21319273   PMID:21423176   PMID:21516116   PMID:21630459   PMID:21726808   PMID:21857917   PMID:21873635   PMID:21942715   PMID:22145905   PMID:22174317   PMID:22586326   PMID:22623428  
PMID:22658674   PMID:22681889   PMID:22863883   PMID:22939629   PMID:22944692   PMID:23184937   PMID:23246001   PMID:23398456   PMID:23438482   PMID:23443559   PMID:23455922   PMID:23463506  
PMID:23612971   PMID:23686814   PMID:23979707   PMID:24332808   PMID:24457600   PMID:24711643   PMID:24965446   PMID:24980433   PMID:25144556   PMID:25147182   PMID:25324306   PMID:25416956  
PMID:25437307   PMID:25593309   PMID:25901680   PMID:25921289   PMID:25948554   PMID:25963833   PMID:26170170   PMID:26186194   PMID:26209609   PMID:26344197   PMID:26460568   PMID:26496610  
PMID:26549023   PMID:26673895   PMID:26693507   PMID:26816005   PMID:26831064   PMID:26990986   PMID:27025967   PMID:27049334   PMID:27503909   PMID:27591049   PMID:27684187   PMID:27976729  
PMID:28302793   PMID:28416769   PMID:28443643   PMID:28514442   PMID:28515276   PMID:28561026   PMID:28581483   PMID:28666385   PMID:28902428   PMID:28927264   PMID:28977470   PMID:28977666  
PMID:29117863   PMID:29169044   PMID:29228324   PMID:29229926   PMID:29298432   PMID:29331416   PMID:29395067   PMID:29449217   PMID:29467282   PMID:29507755   PMID:29511296   PMID:29568061  
PMID:29721183   PMID:29777862   PMID:29802200   PMID:29844126   PMID:29845934   PMID:29955894   PMID:29991511   PMID:30021884   PMID:30154076   PMID:30209976   PMID:30274258   PMID:30320934  
PMID:30344098   PMID:30404004   PMID:30442662   PMID:30455355   PMID:30459231   PMID:30463901   PMID:30745168   PMID:30804502   PMID:30890647   PMID:30940648   PMID:30948266   PMID:30997501  
PMID:31048545   PMID:31152661   PMID:31180492   PMID:31239290   PMID:31253590   PMID:31300519   PMID:31405213   PMID:31476572   PMID:31501420   PMID:31586073   PMID:31620119   PMID:31665637  
PMID:31732153   PMID:31751430   PMID:31796584   PMID:31995728   PMID:32041737   PMID:32129710   PMID:32457219   PMID:32529326   PMID:32552912   PMID:32665550   PMID:32694731   PMID:32698014  
PMID:32807901   PMID:32814086   PMID:32850835   PMID:32905556   PMID:32929329   PMID:32994395   PMID:33080218   PMID:33194618   PMID:33226137   PMID:33239621   PMID:33277362   PMID:33306668  
PMID:33567341   PMID:33644029   PMID:33658012   PMID:33729478   PMID:33762435   PMID:33766124   PMID:33838681   PMID:33869196   PMID:33916271   PMID:33957083   PMID:33961781   PMID:33989516  
PMID:34077860   PMID:34079125   PMID:34091597   PMID:34185411   PMID:34226595   PMID:34244565   PMID:34373451   PMID:34428256   PMID:34431227   PMID:34462429   PMID:34516797   PMID:34537242  
PMID:34650049   PMID:34728620   PMID:35013218   PMID:35031058   PMID:35140242   PMID:35152003   PMID:35256949   PMID:35271311   PMID:35338135   PMID:35446349   PMID:35509820   PMID:35562734  
PMID:35563538   PMID:35605301   PMID:35676659   PMID:35819319   PMID:35831314   PMID:35831895   PMID:35844135   PMID:35850772   PMID:35864588   PMID:35944360   PMID:35973989   PMID:36042349  
PMID:36057605   PMID:36114006   PMID:36129980   PMID:36180527   PMID:36180891   PMID:36199071   PMID:36215168   PMID:36307841   PMID:36321656   PMID:36339263   PMID:36373674   PMID:36424410  
PMID:36517590   PMID:36526897   PMID:36537216   PMID:36574265   PMID:36584595   PMID:36634849   PMID:36779763   PMID:36811957   PMID:37120454   PMID:37616343   PMID:37827155   PMID:38113892  
PMID:38172120   PMID:38245532  


Genomics

Comparative Map Data
RPS3A
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh384151,099,628 - 151,104,642 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl4151,099,624 - 151,104,642 (+)EnsemblGRCh38hg38GRCh38
GRCh374152,020,780 - 152,025,794 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 364152,240,204 - 152,245,254 (+)NCBINCBI36Build 36hg18NCBI36
Build 344152,378,388 - 152,383,393NCBI
Celera4149,342,420 - 149,347,475 (+)NCBICelera
Cytogenetic Map4q31.3NCBI
HuRef4147,746,045 - 147,751,132 (+)NCBIHuRef
CHM1_14151,997,753 - 152,002,834 (+)NCBICHM1_1
T2T-CHM13v2.04154,423,512 - 154,428,526 (+)NCBIT2T-CHM13v2.0
Rps3a1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39386,045,247 - 86,049,975 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl386,045,247 - 86,050,009 (-)EnsemblGRCm39 Ensembl
GRCm38386,137,940 - 86,142,668 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl386,137,940 - 86,142,702 (-)EnsemblGRCm38mm10GRCm38
MGSCv37385,941,862 - 85,946,590 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36386,223,873 - 86,228,520 (-)NCBIMGSCv36mm8
Celera386,163,967 - 86,168,610 (-)NCBICelera
Cytogenetic Map3F1NCBI
cM Map337.83NCBI
Rps3a
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82173,822,673 - 173,827,042 (-)NCBIGRCr8
mRatBN7.22171,524,685 - 171,529,054 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2171,524,500 - 171,529,055 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx2178,678,755 - 178,683,124 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.02176,698,691 - 176,703,060 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.02171,300,509 - 171,304,870 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.02185,440,477 - 185,444,846 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl2185,440,291 - 185,444,897 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.02204,831,252 - 204,835,621 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42178,092,351 - 178,096,720 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.12178,042,456 - 178,046,826 (-)NCBI
Celera2165,497,425 - 165,501,795 (-)NCBICelera
Cytogenetic Map2q34NCBI
Rps3a
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554715,705,829 - 5,710,683 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554715,705,829 - 5,710,683 (+)NCBIChiLan1.0ChiLan1.0
LOC100975318
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v23148,982,386 - 148,987,600 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan14149,339,875 - 149,345,092 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v04143,438,184 - 143,443,266 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.14155,092,898 - 155,097,954 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl4155,092,898 - 155,097,953 (+)Ensemblpanpan1.1panPan2
RPS3A
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11549,066,636 - 49,071,012 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1549,066,705 - 49,071,012 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1549,404,642 - 49,409,019 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01549,742,595 - 49,746,972 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1549,742,680 - 49,749,194 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11549,011,324 - 49,015,708 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01549,104,917 - 49,109,293 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01549,429,825 - 49,434,209 (+)NCBIUU_Cfam_GSD_1.0
Rps3a
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440530141,392,090 - 41,396,701 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366891,134,547 - 1,139,161 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366891,134,565 - 1,139,161 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RPS3A
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl877,889,607 - 78,023,346 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1877,889,616 - 77,893,740 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2882,594,439 - 82,598,565 (-)NCBISscrofa10.2Sscrofa10.2susScr3

Variants

.
Variants in RPS3A
4 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 4q31.3(chr4:150703713-151282758)x3 copy number gain See cases [RCV000051636] Chr4:150703713..151282758 [GRCh38]
Chr4:151624865..152203910 [GRCh37]
Chr4:151844315..152423360 [NCBI36]
Chr4:4q31.3
uncertain significance
GRCh38/hg38 4q26-35.2(chr4:118065569-190042639)x3 copy number gain See cases [RCV000051785] Chr4:118065569..190042639 [GRCh38]
Chr4:118986724..190828225 [GRCh37]
Chr4:119206172..191200788 [NCBI36]
Chr4:4q26-35.2
pathogenic
GRCh38/hg38 4q27-35.2(chr4:121518223-190062270)x3 copy number gain See cases [RCV000051786] Chr4:121518223..190062270 [GRCh38]
Chr4:122439378..190828225 [GRCh37]
Chr4:122658828..191220419 [NCBI36]
Chr4:4q27-35.2
pathogenic
GRCh38/hg38 4q31.21-31.3(chr4:140876253-152186578)x3 copy number gain See cases [RCV000051787] Chr4:140876253..152186578 [GRCh38]
Chr4:141797407..153107730 [GRCh37]
Chr4:142016857..153327180 [NCBI36]
Chr4:4q31.21-31.3
pathogenic
GRCh38/hg38 4q31.22-34.1(chr4:147317283-173675559)x3 copy number gain See cases [RCV000051788] Chr4:147317283..173675559 [GRCh38]
Chr4:148238435..174596710 [GRCh37]
Chr4:148457885..174833285 [NCBI36]
Chr4:4q31.22-34.1
pathogenic
GRCh38/hg38 4q31.23-35.2(chr4:148356485-189548183)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051789]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051789]|See cases [RCV000051789] Chr4:148356485..189548183 [GRCh38]
Chr4:149277637..190469337 [GRCh37]
Chr4:149497087..190706331 [NCBI36]
Chr4:4q31.23-35.2
pathogenic
GRCh38/hg38 4q22.2-32.3(chr4:92913386-165299707)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051775]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051775]|See cases [RCV000051775] Chr4:92913386..165299707 [GRCh38]
Chr4:93834537..166220859 [GRCh37]
Chr4:94053560..166440309 [NCBI36]
Chr4:4q22.2-32.3
pathogenic
GRCh38/hg38 4q31.21-35.2(chr4:145042668-189975519)x3 copy number gain See cases [RCV000135845] Chr4:145042668..189975519 [GRCh38]
Chr4:145963820..190828225 [GRCh37]
Chr4:146183270..191133668 [NCBI36]
Chr4:4q31.21-35.2
pathogenic
GRCh38/hg38 4q31.1-35.2(chr4:138510532-189963195)x3 copy number gain See cases [RCV000136810] Chr4:138510532..189963195 [GRCh38]
Chr4:139431686..190828225 [GRCh37]
Chr4:139651136..191121344 [NCBI36]
Chr4:4q31.1-35.2
pathogenic
GRCh38/hg38 4q28.3-35.2(chr4:131985253-190095391)x3 copy number gain See cases [RCV000137721] Chr4:131985253..190095391 [GRCh38]
Chr4:132906408..190828225 [GRCh37]
Chr4:133125858..191250527 [NCBI36]
Chr4:4q28.3-35.2
pathogenic|likely benign
GRCh38/hg38 4q28.1-35.1(chr4:125432943-185761887)x3 copy number gain See cases [RCV000138578] Chr4:125432943..185761887 [GRCh38]
Chr4:126354098..186683041 [GRCh37]
Chr4:126573548..186920035 [NCBI36]
Chr4:4q28.1-35.1
pathogenic|likely benign
GRCh38/hg38 4q28.3-35.2(chr4:134935616-190036318)x3 copy number gain See cases [RCV000143559] Chr4:134935616..190036318 [GRCh38]
Chr4:135856771..190957473 [GRCh37]
Chr4:136076221..191194467 [NCBI36]
Chr4:4q28.3-35.2
pathogenic
GRCh37/hg19 4q28.3-35.1(chr4:136912336-184253252)x3 copy number gain See cases [RCV000240245] Chr4:136912336..184253252 [GRCh37]
Chr4:4q28.3-35.1
pathogenic
GRCh37/hg19 4q26-35.2(chr4:119437495-190904301)x3 copy number gain See cases [RCV000240392] Chr4:119437495..190904301 [GRCh37]
Chr4:4q26-35.2
pathogenic
GRCh37/hg19 4q31.3(chr4:151678774-152069336)x3 copy number gain See cases [RCV000446436] Chr4:151678774..152069336 [GRCh37]
Chr4:4q31.3
likely benign
GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3 copy number gain See cases [RCV000446653] Chr4:12440..190904441 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q31.3(chr4:151668145-152071599)x3 copy number gain See cases [RCV000446562] Chr4:151668145..152071599 [GRCh37]
Chr4:4q31.3
uncertain significance
GRCh37/hg19 4q31.3(chr4:152021579-152092541)x3 copy number gain See cases [RCV000445802] Chr4:152021579..152092541 [GRCh37]
Chr4:4q31.3
likely benign
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473) copy number gain See cases [RCV000510453] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q25-35.2(chr4:109199664-189752726)x3 copy number gain See cases [RCV000511945] Chr4:109199664..189752726 [GRCh37]
Chr4:4q25-35.2
pathogenic
GRCh37/hg19 4q22.1-35.2(chr4:93071152-190957473)x3 copy number gain See cases [RCV000510970] Chr4:93071152..190957473 [GRCh37]
Chr4:4q22.1-35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3 copy number gain See cases [RCV000512241] Chr4:68346..190957473 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q31.3(chr4:151678774-152065504)x3 copy number gain not provided [RCV000659192] Chr4:151678774..152065504 [GRCh37]
Chr4:4q31.3
likely benign
GRCh37/hg19 4q31.3(chr4:151603065-152213113)x3 copy number gain not provided [RCV000682467] Chr4:151603065..152213113 [GRCh37]
Chr4:4q31.3
uncertain significance
GRCh37/hg19 4q31.3(chr4:151668145-152073515)x3 copy number gain not provided [RCV000682468] Chr4:151668145..152073515 [GRCh37]
Chr4:4q31.3
uncertain significance
GRCh37/hg19 4q31.3(chr4:151948130-152446550)x3 copy number gain not provided [RCV000682469] Chr4:151948130..152446550 [GRCh37]
Chr4:4q31.3
likely benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190915650)x3 copy number gain not provided [RCV000743155] Chr4:49450..190915650 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4q31.3(chr4:151677255-152069909)x3 copy number gain not provided [RCV000744051] Chr4:151677255..152069909 [GRCh37]
Chr4:4q31.3
benign
GRCh37/hg19 4q31.3(chr4:151694950-152055073)x3 copy number gain not provided [RCV000744052] Chr4:151694950..152055073 [GRCh37]
Chr4:4q31.3
benign
GRCh37/hg19 4p16.3-q35.2(chr4:49450-190963766)x3 copy number gain not provided [RCV000743156] Chr4:49450..190963766 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
GRCh37/hg19 4p16.3-q35.2(chr4:11525-191028879)x3 copy number gain not provided [RCV000743147] Chr4:11525..191028879 [GRCh37]
Chr4:4p16.3-q35.2
pathogenic
NM_001006.5(RPS3A):c.63-6A>T single nucleotide variant not provided [RCV000958761] Chr4:151100479 [GRCh38]
Chr4:152021631 [GRCh37]
Chr4:4q31.3
benign
GRCh37/hg19 4q31.3-35.2(chr4:151174061-190957473)x3 copy number gain not provided [RCV000849098] Chr4:151174061..190957473 [GRCh37]
Chr4:4q31.3-35.2
pathogenic
GRCh37/hg19 4q28.1-35.1(chr4:124873497-185278662)x3 copy number gain not provided [RCV000849686] Chr4:124873497..185278662 [GRCh37]
Chr4:4q28.1-35.1
pathogenic
GRCh37/hg19 4q28.3-32.3(chr4:131303317-168722402)x3 copy number gain not provided [RCV001537926] Chr4:131303317..168722402 [GRCh37]
Chr4:4q28.3-32.3
pathogenic
NM_001006.5(RPS3A):c.373G>A (p.Val125Ile) single nucleotide variant Inborn genetic diseases [RCV002969644] Chr4:151102889 [GRCh38]
Chr4:152024041 [GRCh37]
Chr4:4q31.3
uncertain significance
NM_001006.5(RPS3A):c.383A>G (p.Lys128Arg) single nucleotide variant Inborn genetic diseases [RCV002950441] Chr4:151102899 [GRCh38]
Chr4:152024051 [GRCh37]
Chr4:4q31.3
uncertain significance
NM_001006.5(RPS3A):c.737C>A (p.Thr246Lys) single nucleotide variant Inborn genetic diseases [RCV002644825] Chr4:151104535 [GRCh38]
Chr4:152025687 [GRCh37]
Chr4:4q31.3
uncertain significance
GRCh37/hg19 4q26-32.3(chr4:117518683-168174703)x3 copy number gain not provided [RCV003484198] Chr4:117518683..168174703 [GRCh37]
Chr4:4q26-32.3
pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1307
Count of miRNA genes:622
Interacting mature miRNAs:712
Transcripts:ENST00000274065, ENST00000322686, ENST00000503002, ENST00000505243, ENST00000506126, ENST00000507327, ENST00000507485, ENST00000508783, ENST00000509736, ENST00000510993, ENST00000512690, ENST00000512797, ENST00000514682, ENST00000515792, ENST00000515818
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-59322  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh374152,025,448 - 152,025,632UniSTSGRCh37
Build 364152,244,898 - 152,245,082RGDNCBI36
Celera4149,347,119 - 149,347,303RGD
Cytogenetic Map4q31.2-q31.3UniSTS
HuRef4147,750,773 - 147,750,960UniSTS
GeneMap99-GB4 RH Map4635.8UniSTS
Whitehead-RH Map4684.4UniSTS
Whitehead-YAC Contig Map4 UniSTS
NCBI RH Map41568.4UniSTS
D4S2325  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q31.2-q31.3UniSTS
GDB:554881  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map4q31.2-q31.3UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High 1038 987 530 88 630 34 2832 413 610 159 876 851 61 814 1602 3
Medium 1394 1995 1195 534 1317 430 1523 1782 3114 259 574 758 112 390 1186 1
Low 7 9 1 2 4 1 1 2 10 1 10 4 2 1 2 2
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001006 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001267699 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB007148 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB062070 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC095055 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI038646 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK129825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK296121 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK308947 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK311788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC000204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004981 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006298 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009219 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC009404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC017123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018954 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066926 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC070211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071916 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ055367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA441711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471056 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CN315189 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX754149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D16953 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D16985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D17120 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D28374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L13802 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M77234 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M84711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X87373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000274065   ⟹   ENSP00000346050
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,628 - 151,104,642 (+)Ensembl
RefSeq Acc Id: ENST00000503002   ⟹   ENSP00000421277
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,631 - 151,101,114 (+)Ensembl
RefSeq Acc Id: ENST00000505243   ⟹   ENSP00000425024
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,628 - 151,102,932 (+)Ensembl
RefSeq Acc Id: ENST00000506126   ⟹   ENSP00000426282
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,674 - 151,104,623 (+)Ensembl
RefSeq Acc Id: ENST00000507327   ⟹   ENSP00000424547
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,669 - 151,104,490 (+)Ensembl
RefSeq Acc Id: ENST00000507485
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,628 - 151,104,205 (+)Ensembl
RefSeq Acc Id: ENST00000508783   ⟹   ENSP00000421776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,640 - 151,103,004 (+)Ensembl
RefSeq Acc Id: ENST00000509736   ⟹   ENSP00000422994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,624 - 151,104,637 (+)Ensembl
RefSeq Acc Id: ENST00000510993   ⟹   ENSP00000426466
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,873 - 151,104,528 (+)Ensembl
RefSeq Acc Id: ENST00000512690   ⟹   ENSP00000423953
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,639 - 151,104,637 (+)Ensembl
RefSeq Acc Id: ENST00000512797   ⟹   ENSP00000421457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,668 - 151,104,537 (+)Ensembl
RefSeq Acc Id: ENST00000514682   ⟹   ENSP00000421770
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,629 - 151,104,637 (+)Ensembl
RefSeq Acc Id: ENST00000515792   ⟹   ENSP00000425508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,671 - 151,104,637 (+)Ensembl
RefSeq Acc Id: ENST00000515818   ⟹   ENSP00000425978
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl4151,099,629 - 151,104,238 (+)Ensembl
RefSeq Acc Id: NM_001006   ⟹   NP_000997
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384151,099,628 - 151,104,642 (+)NCBI
GRCh374152,020,725 - 152,025,804 (+)NCBI
Build 364152,240,204 - 152,245,254 (+)NCBI Archive
HuRef4147,746,045 - 147,751,132 (+)NCBI
CHM1_14151,997,753 - 152,002,834 (+)NCBI
T2T-CHM13v2.04154,423,512 - 154,428,526 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001267699   ⟹   NP_001254628
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh384151,099,628 - 151,104,198 (+)NCBI
GRCh374152,020,725 - 152,025,804 (+)NCBI
HuRef4147,746,045 - 147,751,132 (+)NCBI
CHM1_14151,997,753 - 152,002,390 (+)NCBI
T2T-CHM13v2.04154,423,512 - 154,428,082 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_000997 (Get FASTA)   NCBI Sequence Viewer  
  NP_001254628 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA35682 (Get FASTA)   NCBI Sequence Viewer  
  AAA58487 (Get FASTA)   NCBI Sequence Viewer  
  AAA60290 (Get FASTA)   NCBI Sequence Viewer  
  AAH00204 (Get FASTA)   NCBI Sequence Viewer  
  AAH01708 (Get FASTA)   NCBI Sequence Viewer  
  AAH04981 (Get FASTA)   NCBI Sequence Viewer  
  AAH06298 (Get FASTA)   NCBI Sequence Viewer  
  AAH09219 (Get FASTA)   NCBI Sequence Viewer  
  AAH09404 (Get FASTA)   NCBI Sequence Viewer  
  AAH17123 (Get FASTA)   NCBI Sequence Viewer  
  AAH66926 (Get FASTA)   NCBI Sequence Viewer  
  AAH70211 (Get FASTA)   NCBI Sequence Viewer  
  AAH71916 (Get FASTA)   NCBI Sequence Viewer  
  BAA05740 (Get FASTA)   NCBI Sequence Viewer  
  BAA25814 (Get FASTA)   NCBI Sequence Viewer  
  BAF83764 (Get FASTA)   NCBI Sequence Viewer  
  BAG34731 (Get FASTA)   NCBI Sequence Viewer  
  BAH12261 (Get FASTA)   NCBI Sequence Viewer  
  CAA60827 (Get FASTA)   NCBI Sequence Viewer  
  EAX04988 (Get FASTA)   NCBI Sequence Viewer  
  EAX04989 (Get FASTA)   NCBI Sequence Viewer  
  EAX04990 (Get FASTA)   NCBI Sequence Viewer  
  EAX04991 (Get FASTA)   NCBI Sequence Viewer  
  EAX04992 (Get FASTA)   NCBI Sequence Viewer  
  EAX04993 (Get FASTA)   NCBI Sequence Viewer  
  EAX04994 (Get FASTA)   NCBI Sequence Viewer  
  EAX04995 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000346050
  ENSP00000346050.3
  ENSP00000421277.1
  ENSP00000421457.1
  ENSP00000421770.1
  ENSP00000421776.1
  ENSP00000422994.1
  ENSP00000423953.1
  ENSP00000424547.1
  ENSP00000425024.1
  ENSP00000425508.1
  ENSP00000425978.1
  ENSP00000426282.1
  ENSP00000426466.1
  ENSP00000517921.1
GenBank Protein P61247 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_000997   ⟸   NM_001006
- Peptide Label: isoform 1
- UniProtKB: P33443 (UniProtKB/Swiss-Prot),   D3DP05 (UniProtKB/Swiss-Prot),   B2R4D4 (UniProtKB/Swiss-Prot),   P49241 (UniProtKB/Swiss-Prot),   P61247 (UniProtKB/Swiss-Prot),   A8K4W0 (UniProtKB/TrEMBL),   Q6NXR8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001254628   ⟸   NM_001267699
- Peptide Label: isoform 2
- UniProtKB: B7Z3M5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000421277   ⟸   ENST00000503002
RefSeq Acc Id: ENSP00000425024   ⟸   ENST00000505243
RefSeq Acc Id: ENSP00000426282   ⟸   ENST00000506126
RefSeq Acc Id: ENSP00000424547   ⟸   ENST00000507327
RefSeq Acc Id: ENSP00000421776   ⟸   ENST00000508783
RefSeq Acc Id: ENSP00000422994   ⟸   ENST00000509736
RefSeq Acc Id: ENSP00000346050   ⟸   ENST00000274065
RefSeq Acc Id: ENSP00000426466   ⟸   ENST00000510993
RefSeq Acc Id: ENSP00000421457   ⟸   ENST00000512797
RefSeq Acc Id: ENSP00000423953   ⟸   ENST00000512690
RefSeq Acc Id: ENSP00000421770   ⟸   ENST00000514682
RefSeq Acc Id: ENSP00000425978   ⟸   ENST00000515818
RefSeq Acc Id: ENSP00000425508   ⟸   ENST00000515792

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P61247-F1-model_v2 AlphaFold P61247 1-264 view protein structure

Promoters
RGD ID:6868660
Promoter ID:EPDNEW_H7495
Type:initiation region
Name:RPS3A_1
Description:ribosomal protein S3A
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh384151,099,629 - 151,099,689EPDNEW
RGD ID:6802577
Promoter ID:HG_KWN:49267
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001006
Position:
Human AssemblyChrPosition (strand)Source
Build 364152,239,901 - 152,240,401 (+)MPROMDB
RGD ID:6853366
Promoter ID:EP74493
Type:multiple initiation site
Name:HS_RPS3A
Description:Ribosomal protein S3A.
SO ACC ID:SO:0000170
Source:EPD (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Mammalian gene collection (MGC) full-length cDNA cloning
Position:No map positions available.

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10421 AgrOrtholog
COSMIC RPS3A COSMIC
Ensembl Genes ENSG00000145425 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSG00000292158 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000274065 ENTREZGENE
  ENST00000274065.9 UniProtKB/Swiss-Prot
  ENST00000503002.5 UniProtKB/TrEMBL
  ENST00000505243.5 UniProtKB/TrEMBL
  ENST00000506126.5 UniProtKB/TrEMBL
  ENST00000507327.5 UniProtKB/TrEMBL
  ENST00000507485 ENTREZGENE
  ENST00000508783.5 UniProtKB/TrEMBL
  ENST00000509736.5 UniProtKB/TrEMBL
  ENST00000510993.1 UniProtKB/TrEMBL
  ENST00000512690.5 UniProtKB/TrEMBL
  ENST00000512797.5 UniProtKB/TrEMBL
  ENST00000514682.5 UniProtKB/TrEMBL
  ENST00000515792.5 UniProtKB/TrEMBL
  ENST00000515818.5 UniProtKB/TrEMBL
  ENST00000709893.1 UniProtKB/Swiss-Prot
GTEx ENSG00000145425 GTEx
  ENSG00000292158 GTEx
HGNC ID HGNC:10421 ENTREZGENE
Human Proteome Map RPS3A Human Proteome Map
InterPro Ribosomal_S1/3_euk UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S3Ae UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S3Ae_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6189 UniProtKB/Swiss-Prot
NCBI Gene 6189 ENTREZGENE
OMIM 180478 OMIM
PANTHER 40S RIBOSOMAL PROTEIN S3A UniProtKB/Swiss-Prot
  40S RIBOSOMAL PROTEIN S3A UniProtKB/Swiss-Prot
  40S RIBOSOMAL PROTEIN S3A UniProtKB/TrEMBL
  40S RIBOSOMAL PROTEIN S3A UniProtKB/TrEMBL
  40S RIBOSOMAL PROTEIN S3A UniProtKB/TrEMBL
Pfam Ribosomal_S3Ae UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34830 PharmGKB
PROSITE RIBOSOMAL_S3AE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART Ribosomal_S3Ae UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8K4W0 ENTREZGENE, UniProtKB/TrEMBL
  B2R4D4 ENTREZGENE
  B7Z3M5 ENTREZGENE, UniProtKB/TrEMBL
  D3DP05 ENTREZGENE
  D6R9B6_HUMAN UniProtKB/TrEMBL
  D6RAS7_HUMAN UniProtKB/TrEMBL
  D6RAT0_HUMAN UniProtKB/TrEMBL
  D6RB09_HUMAN UniProtKB/TrEMBL
  D6RED7_HUMAN UniProtKB/TrEMBL
  D6RG13_HUMAN UniProtKB/TrEMBL
  D6RGE0_HUMAN UniProtKB/TrEMBL
  D6RI02_HUMAN UniProtKB/TrEMBL
  E9PFI5_HUMAN UniProtKB/TrEMBL
  H0Y8L7_HUMAN UniProtKB/TrEMBL
  H0Y9Y4_HUMAN UniProtKB/TrEMBL
  P33443 ENTREZGENE
  P49241 ENTREZGENE
  P61247 ENTREZGENE
  Q6NXR8 ENTREZGENE, UniProtKB/TrEMBL
  RS3A_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2R4D4 UniProtKB/Swiss-Prot
  D3DP05 UniProtKB/Swiss-Prot
  P33443 UniProtKB/Swiss-Prot
  P49241 UniProtKB/Swiss-Prot