RPS2 (ribosomal protein S2) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: RPS2 (ribosomal protein S2) Homo sapiens
Analyze
Symbol: RPS2
Name: ribosomal protein S2
RGD ID: 732314
HGNC Page HGNC
Description: Enables enzyme binding activity; fibroblast growth factor binding activity; and mRNA binding activity. A structural constituent of ribosome. Involved in positive regulation of ubiquitin-protein transferase activity. Located in cytosolic ribosome and nucleoplasm. Part of cytosolic small ribosomal subunit.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: 40S ribosomal protein S2; 40S ribosomal protein S4; LLREP3; MGC102851; MGC117344; MGC117345; OK/KNS-cl.6; S2; small ribosomal subunit protein uS5
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: AC007956.2   AC087163.1   AL035690.1   LOC100419257   LOC148430   RPS2P1   RPS2P10   RPS2P11   RPS2P12   RPS2P13   RPS2P14   RPS2P15   RPS2P16   RPS2P17   RPS2P18   RPS2P19   RPS2P2   RPS2P20   RPS2P21   RPS2P22   RPS2P23   RPS2P24   RPS2P25   RPS2P26   RPS2P27   RPS2P28   RPS2P29   RPS2P3   RPS2P30   RPS2P31   RPS2P32   RPS2P33   RPS2P34   RPS2P35   RPS2P36   RPS2P37   RPS2P38   RPS2P39   RPS2P4   RPS2P40   RPS2P41   RPS2P42   RPS2P43   RPS2P44   RPS2P45   RPS2P46   RPS2P47   RPS2P48   RPS2P49   RPS2P5   RPS2P50   RPS2P51   RPS2P52   RPS2P53   RPS2P54   RPS2P55   RPS2P6   RPS2P7   RPS2P8   RPS2P9  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl161,962,058 - 1,964,841 (-)EnsemblGRCh38hg38GRCh38
GRCh38161,962,058 - 1,964,826 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37162,012,059 - 2,014,827 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36161,952,063 - 1,954,828 (-)NCBINCBI36hg18NCBI36
Build 34161,952,062 - 1,954,630NCBI
Celera162,224,244 - 2,227,009 (-)NCBI
Cytogenetic Map16p13.3NCBI
HuRef161,936,189 - 1,938,954 (-)NCBIHuRef
CHM1_1162,012,008 - 2,014,773 (-)NCBICHM1_1
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-dimethylhydrazine  (ISO)
17alpha-ethynylestradiol  (ISO)
2,2',4,4'-Tetrabromodiphenyl ether  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2,3,7,8-Tetrachlorodibenzofuran  (ISO)
2,4,6-trinitrotoluene  (ISO)
2,6-dinitrotoluene  (ISO)
2-hydroxypropanoic acid  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
3-isobutyl-1-methyl-7H-xanthine  (EXP)
acetamide  (ISO)
acrolein  (EXP)
aflatoxin B1  (ISO)
all-trans-retinoic acid  (EXP)
alpha-pinene  (EXP)
ammonium chloride  (ISO)
antimycin A  (EXP)
aristolochic acid  (EXP)
Aroclor 1254  (ISO)
astaxanthin  (ISO)
azoxystrobin  (EXP)
benzo[a]pyrene  (ISO)
bexarotene  (ISO)
bisphenol A  (EXP,ISO)
bromobenzene  (ISO)
C60 fullerene  (ISO)
carbon nanotube  (EXP,ISO)
chloropicrin  (EXP)
chromium(6+)  (ISO)
clofibric acid  (ISO)
copper atom  (EXP)
copper(0)  (EXP)
copper(II) sulfate  (EXP)
CU-O LINKAGE  (EXP)
deguelin  (EXP)
dexamethasone  (EXP)
diazinon  (EXP)
dibutyl phthalate  (ISO)
enzyme inhibitor  (EXP)
ethanol  (ISO)
fenpyroximate  (EXP)
flavonoids  (ISO)
flutamide  (ISO)
folic acid  (ISO)
formaldehyde  (EXP)
furan  (ISO)
gentamycin  (ISO)
hydralazine  (EXP)
indometacin  (EXP)
ivermectin  (EXP)
methotrexate  (ISO)
methylisothiazolinone  (EXP)
N-nitrosodiethylamine  (ISO)
nefazodone  (ISO)
nimesulide  (ISO)
ozone  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
PhIP  (ISO)
pyrimidifen  (EXP)
rac-lactic acid  (EXP)
rotenone  (ISO)
sodium arsenite  (ISO)
sodium fluoride  (ISO)
Soman  (ISO)
tamibarotene  (EXP)
temozolomide  (EXP)
tetrachloromethane  (ISO)
titanium dioxide  (ISO)
tungsten  (ISO)
valproic acid  (EXP,ISO)

Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Seizure  (IAGP)
References

Additional References at PubMed
PMID:2308862   PMID:6188845   PMID:8706699   PMID:8722009   PMID:9582194   PMID:11751223   PMID:12422231   PMID:12477932   PMID:12588972   PMID:12694581   PMID:12882984   PMID:15189156  
PMID:15303970   PMID:15324660   PMID:15473865   PMID:15489334   PMID:15635413   PMID:15883184   PMID:16051665   PMID:16061210   PMID:16159877   PMID:16169070   PMID:16263090   PMID:16964243  
PMID:17081983   PMID:17361185   PMID:17620599   PMID:17643375   PMID:18457437   PMID:18464793   PMID:18573314   PMID:19138403   PMID:19287380   PMID:19738201   PMID:19805454   PMID:19946888  
PMID:20020773   PMID:20458337   PMID:20811636   PMID:21081503   PMID:21145461   PMID:21182205   PMID:21319273   PMID:21423176   PMID:21584310   PMID:21630459   PMID:21873635   PMID:21900206  
PMID:21942715   PMID:21963895   PMID:21988832   PMID:22145905   PMID:22174317   PMID:22586326   PMID:22623428   PMID:22658674   PMID:22681889   PMID:22751105   PMID:22863883   PMID:22939629  
PMID:23084401   PMID:23125841   PMID:23166591   PMID:23246001   PMID:23376485   PMID:23398456   PMID:23443559   PMID:23463506   PMID:23612971   PMID:23824909   PMID:24189400   PMID:24244333  
PMID:24457600   PMID:24625528   PMID:24711643   PMID:24725412   PMID:24965446   PMID:24980433   PMID:24981860   PMID:25144556   PMID:25315684   PMID:25324306   PMID:25437307   PMID:25468996  
PMID:25737013   PMID:25756610   PMID:25798074   PMID:25921289   PMID:25948554   PMID:26170170   PMID:26186194   PMID:26209609   PMID:26217791   PMID:26344197   PMID:26362536   PMID:26460568  
PMID:26496610   PMID:26549023   PMID:26561776   PMID:26673895   PMID:26693507   PMID:26725010   PMID:26816005   PMID:26831064   PMID:27025967   PMID:27342126   PMID:27503909   PMID:27576135  
PMID:27591049   PMID:27684187   PMID:27697862   PMID:27976729   PMID:28024152   PMID:28077445   PMID:28302793   PMID:28514442   PMID:28515276   PMID:28561026   PMID:28581483   PMID:28685749  
PMID:28700943   PMID:28902428   PMID:28927264   PMID:28977470   PMID:28977666   PMID:29117863   PMID:29229926   PMID:29298432   PMID:29331416   PMID:29395067   PMID:29467282   PMID:29507755  
PMID:29511296   PMID:29721183   PMID:29802200   PMID:29844126   PMID:29845934   PMID:29859926   PMID:29955894   PMID:29991511   PMID:30021884   PMID:30097533   PMID:30209976   PMID:30258100  
PMID:30320910   PMID:30320934   PMID:30344098   PMID:30404004   PMID:30455355   PMID:30459231   PMID:30463901   PMID:30530495   PMID:30575818   PMID:30626644   PMID:30804502   PMID:30890647  
PMID:30940648   PMID:30948266   PMID:30997501   PMID:31046837   PMID:31048545   PMID:31059266   PMID:31091453   PMID:31180492   PMID:31239290   PMID:31253590   PMID:31501420   PMID:31586073  
PMID:31620119   PMID:31640799   PMID:31665637   PMID:31796584   PMID:31894111   PMID:31928715   PMID:31995728   PMID:32041737   PMID:32129710   PMID:32296183   PMID:32370049   PMID:32457219  
PMID:32529326   PMID:32552912   PMID:32698014   PMID:32788342   PMID:32807901   PMID:32850835   PMID:32877691   PMID:32905556   PMID:32908316   PMID:32929329   PMID:32994395   PMID:33022573  
PMID:33226137   PMID:33245768   PMID:33378683   PMID:33567341   PMID:33644029   PMID:33869196   PMID:33916271   PMID:33961781   PMID:34079125  


Genomics

Comparative Map Data
RPS2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl161,962,058 - 1,964,841 (-)EnsemblGRCh38hg38GRCh38
GRCh38161,962,058 - 1,964,826 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37162,012,059 - 2,014,827 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36161,952,063 - 1,954,828 (-)NCBINCBI36hg18NCBI36
Build 34161,952,062 - 1,954,630NCBI
Celera162,224,244 - 2,227,009 (-)NCBI
Cytogenetic Map16p13.3NCBI
HuRef161,936,189 - 1,938,954 (-)NCBIHuRef
CHM1_1162,012,008 - 2,014,773 (-)NCBICHM1_1
Rps2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391724,939,037 - 24,940,901 (+)NCBIGRCm39mm39
GRCm39 Ensembl1724,937,090 - 24,940,903 (+)Ensembl
GRCm381724,718,121 - 24,721,927 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1724,718,116 - 24,721,929 (+)EnsemblGRCm38mm10GRCm38
MGSCv371724,857,008 - 24,858,872 (+)NCBIGRCm37mm9NCBIm37
MGSCv361724,447,709 - 24,449,522 (+)NCBImm8
Celera1725,243,190 - 25,245,054 (+)NCBICelera
Cytogenetic Map17A3.3NCBI
Rps2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21013,747,316 - 13,749,165 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1013,747,301 - 13,749,163 (+)Ensembl
Rnor_6.01014,088,171 - 14,090,020 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1014,088,319 - 14,089,979 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01013,903,899 - 13,905,748 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41013,975,350 - 13,977,199 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11013,975,494 - 13,977,163 (+)NCBI
Celera1013,427,034 - 13,428,883 (+)NCBICelera
Cytogenetic Map10q12NCBI
Rps2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0NW_00495544215,304,306 - 15,306,599 (+)NCBIChiLan1.0ChiLan1.0
RPS2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1162,051,083 - 2,053,825 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl162,051,128 - 2,054,086 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v016739,562 - 742,323 (+)NCBIMhudiblu_PPA_v0panPan3
RPS2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1638,966,830 - 38,968,743 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha640,206,543 - 40,208,435 (+)NCBI
ROS_Cfam_1.0639,283,871 - 39,285,763 (+)NCBI
UMICH_Zoey_3.1638,960,646 - 38,962,538 (+)NCBI
UNSW_CanFamBas_1.0638,932,954 - 38,934,846 (+)NCBI
UU_Cfam_GSD_1.0639,411,841 - 39,413,733 (+)NCBI
Rps2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024409344104,636,052 - 104,637,992 (-)NCBI
SpeTri2.0NW_0049366942,071,295 - 2,073,409 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
RPS2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl339,996,174 - 40,003,107 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1339,996,179 - 40,003,110 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
RPS2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.151,859,411 - 1,862,322 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl51,859,454 - 1,862,305 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366606829,205,593 - 29,217,053 (+)NCBIVero_WHO_p1.0
Rps2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_004624913295,554 - 297,588 (+)NCBIHetGla_female_1.0hetGla2

Position Markers
RP_S2_1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,012,291 - 2,012,504UniSTSGRCh37
Build 36161,952,292 - 1,952,505RGDNCBI36
Celera162,224,473 - 2,224,686RGD
Cytogenetic Map16p13.3UniSTS
HuRef161,936,418 - 1,936,631UniSTS
G54162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37162,013,869 - 2,014,169UniSTSGRCh37
Build 36161,953,870 - 1,954,170RGDNCBI36
Celera162,226,051 - 2,226,351RGD
Cytogenetic Map16p13.3UniSTS
HuRef161,937,996 - 1,938,296UniSTS
RH65663  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1q23.3-q24.1UniSTS
Cytogenetic Map16p13.3UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR330hsa-miR-330-3pMirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248
MIR3943hsa-miR-3943Mirtarbaseexternal_infoCLASHFunctional MTI (Weak)23622248

Predicted Target Of
Summary Value
Count of predictions:4084
Count of miRNA genes:940
Interacting mature miRNAs:1113
Transcripts:ENST00000343262, ENST00000526522, ENST00000526586, ENST00000526908, ENST00000527109, ENST00000527302, ENST00000527826, ENST00000527871, ENST00000529806, ENST00000530225, ENST00000531065, ENST00000532746, ENST00000533161, ENST00000533186, ENST00000533872, ENST00000534461, ENST00000563194
Prediction methods:Microtar, Miranda, Rnahybrid
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.


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 1444 993 693 172 1090 68 3247 783 728 169 1024 1115 117 1033 1754 3
Medium 995 1996 1032 452 861 397 1109 1413 2991 249 432 497 57 1 171 1034 3 2
Low 2 1 1 1 15 1 4 1 1
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_002952 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB007147 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB065088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB065089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AB082925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC005363 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312173 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL832857 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001795 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC004520 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC006559 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008329 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC008862 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC010165 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012354 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC013833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016178 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC016951 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC019021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC021545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC023541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC025677 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC029979 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC032129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC035427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC052235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC063011 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC066321 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC068051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071673 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071922 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC073966 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC075830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC103756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC105985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC106060 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X17206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000343262   ⟹   ENSP00000341885
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,058 - 1,964,826 (-)Ensembl
RefSeq Acc Id: ENST00000526522   ⟹   ENSP00000436865
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,060 - 1,964,803 (-)Ensembl
RefSeq Acc Id: ENST00000526586   ⟹   ENSP00000460860
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,963,256 (-)Ensembl
RefSeq Acc Id: ENST00000526908
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,643 - 1,964,538 (-)Ensembl
RefSeq Acc Id: ENST00000527109
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,630 (-)Ensembl
RefSeq Acc Id: ENST00000527302   ⟹   ENSP00000433034
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,552 - 1,964,806 (-)Ensembl
RefSeq Acc Id: ENST00000527826
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,950 - 1,964,805 (-)Ensembl
RefSeq Acc Id: ENST00000527871
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,631 (-)Ensembl
RefSeq Acc Id: ENST00000529806   ⟹   ENSP00000433170
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,079 - 1,964,812 (-)Ensembl
RefSeq Acc Id: ENST00000530225   ⟹   ENSP00000436356
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,631 (-)Ensembl
RefSeq Acc Id: ENST00000531065
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,631 (-)Ensembl
RefSeq Acc Id: ENST00000532746   ⟹   ENSP00000434846
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,367 (-)Ensembl
RefSeq Acc Id: ENST00000533161
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,813 (-)Ensembl
RefSeq Acc Id: ENST00000533186   ⟹   ENSP00000436227
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,356 (-)Ensembl
RefSeq Acc Id: ENST00000533872
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,061 - 1,964,581 (-)Ensembl
RefSeq Acc Id: ENST00000534461
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,962,374 - 1,964,365 (-)Ensembl
RefSeq Acc Id: ENST00000563194   ⟹   ENSP00000454837
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl161,963,212 - 1,964,841 (-)Ensembl
RefSeq Acc Id: NM_002952   ⟹   NP_002943
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,962,058 - 1,964,826 (-)NCBI
GRCh37162,012,059 - 2,014,827 (-)NCBI
Build 36161,952,063 - 1,954,828 (-)NCBI Archive
HuRef161,936,189 - 1,938,954 (-)ENTREZGENE
CHM1_1162,012,008 - 2,014,773 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_002943 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH01795 (Get FASTA)   NCBI Sequence Viewer  
  AAH04520 (Get FASTA)   NCBI Sequence Viewer  
  AAH06559 (Get FASTA)   NCBI Sequence Viewer  
  AAH08862 (Get FASTA)   NCBI Sequence Viewer  
  AAH10165 (Get FASTA)   NCBI Sequence Viewer  
  AAH12354 (Get FASTA)   NCBI Sequence Viewer  
  AAH16178 (Get FASTA)   NCBI Sequence Viewer  
  AAH16951 (Get FASTA)   NCBI Sequence Viewer  
  AAH18993 (Get FASTA)   NCBI Sequence Viewer  
  AAH21545 (Get FASTA)   NCBI Sequence Viewer  
  AAH23541 (Get FASTA)   NCBI Sequence Viewer  
  AAH25677 (Get FASTA)   NCBI Sequence Viewer  
  AAH32129 (Get FASTA)   NCBI Sequence Viewer  
  AAH66321 (Get FASTA)   NCBI Sequence Viewer  
  AAH68051 (Get FASTA)   NCBI Sequence Viewer  
  AAH71673 (Get FASTA)   NCBI Sequence Viewer  
  AAH71922 (Get FASTA)   NCBI Sequence Viewer  
  AAH71923 (Get FASTA)   NCBI Sequence Viewer  
  AAH71924 (Get FASTA)   NCBI Sequence Viewer  
  AAH73966 (Get FASTA)   NCBI Sequence Viewer  
  AAH75830 (Get FASTA)   NCBI Sequence Viewer  
  AAI03757 (Get FASTA)   NCBI Sequence Viewer  
  AAI05986 (Get FASTA)   NCBI Sequence Viewer  
  AAI06061 (Get FASTA)   NCBI Sequence Viewer  
  BAA25813 (Get FASTA)   NCBI Sequence Viewer  
  BAB93525 (Get FASTA)   NCBI Sequence Viewer  
  BAB93526 (Get FASTA)   NCBI Sequence Viewer  
  BAC16801 (Get FASTA)   NCBI Sequence Viewer  
  BAG35107 (Get FASTA)   NCBI Sequence Viewer  
  CAA35078 (Get FASTA)   NCBI Sequence Viewer  
  EAW85592 (Get FASTA)   NCBI Sequence Viewer  
  EAW85593 (Get FASTA)   NCBI Sequence Viewer  
  EAW85594 (Get FASTA)   NCBI Sequence Viewer  
  EAW85595 (Get FASTA)   NCBI Sequence Viewer  
  EAW85596 (Get FASTA)   NCBI Sequence Viewer  
  P15880 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_002943   ⟸   NM_002952
- UniProtKB: P15880 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000436356   ⟸   ENST00000530225
RefSeq Acc Id: ENSP00000434846   ⟸   ENST00000532746
RefSeq Acc Id: ENSP00000436227   ⟸   ENST00000533186
RefSeq Acc Id: ENSP00000454837   ⟸   ENST00000563194
RefSeq Acc Id: ENSP00000436865   ⟸   ENST00000526522
RefSeq Acc Id: ENSP00000460860   ⟸   ENST00000526586
RefSeq Acc Id: ENSP00000433034   ⟸   ENST00000527302
RefSeq Acc Id: ENSP00000341885   ⟸   ENST00000343262
RefSeq Acc Id: ENSP00000433170   ⟸   ENST00000529806
Protein Domains
Ribosomal_S5_C   S5 DRBM

Promoters
RGD ID:6815174
Promoter ID:HG_MRA:5733
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:BC007583,   BC020336,   BC035504,   BC040830,   CU677586,   CU677776,   CU680301,   CU689287,   L07393
Position:
Human AssemblyChrPosition (strand)Source
Build 36161,952,221 - 1,952,721 (+)MPROMDB
RGD ID:6793499
Promoter ID:HG_KWN:22745
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:NR_003142,   OTTHUMT00000250613,   UC002CNL.2,   UC002CNM.2,   UC002CNN.2,   UC010BSA.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36161,953,456 - 1,954,872 (+)MPROMDB
RGD ID:7230965
Promoter ID:EPDNEW_H21227
Type:initiation region
Name:RPS2_2
Description:ribosomal protein S2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H21228  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,964,589 - 1,964,649EPDNEW
RGD ID:7230963
Promoter ID:EPDNEW_H21228
Type:initiation region
Name:RPS2_1
Description:ribosomal protein S2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H21227  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38161,964,826 - 1,964,886EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16p13.3-13.13(chr16:23141-11296695)x3 copy number gain See cases [RCV000052367] Chr16:23141..11296695 [GRCh38]
Chr16:73141..11390552 [GRCh37]
Chr16:13141..11298053 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.3(chr16:29941-2560460)x3 copy number gain See cases [RCV000052368] Chr16:29941..2560460 [GRCh38]
Chr16:79941..2610461 [GRCh37]
Chr16:19941..2550462 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:46766-3214623)x3 copy number gain See cases [RCV000052370] Chr16:46766..3214623 [GRCh38]
Chr16:96766..3264623 [GRCh37]
Chr16:36766..3204624 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:1221651-2233773)x3 copy number gain See cases [RCV000052373] Chr16:1221651..2233773 [GRCh38]
Chr16:1271651..2283774 [GRCh37]
Chr16:1211652..2223775 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:1816283-2020966)x3 copy number gain See cases [RCV000052377] Chr16:1816283..2020966 [GRCh38]
Chr16:1866284..2070967 [GRCh37]
Chr16:1806285..2010968 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3(chr16:46766-1997582)x1 copy number loss See cases [RCV000053253] Chr16:46766..1997582 [GRCh38]
Chr16:96766..2047583 [GRCh37]
Chr16:36766..1987584 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3-13.13(chr16:46766-11525516)x3 copy number gain See cases [RCV000133780] Chr16:46766..11525516 [GRCh38]
Chr16:96766..11619372 [GRCh37]
Chr16:36766..11526873 [NCBI36]
Chr16:16p13.3-13.13
pathogenic
GRCh38/hg38 16p13.3(chr16:1850978-2116369)x3 copy number gain See cases [RCV000135695] Chr16:1850978..2116369 [GRCh38]
Chr16:1900979..2166370 [GRCh37]
Chr16:1840980..2106371 [NCBI36]
Chr16:16p13.3
uncertain significance
GRCh38/hg38 16p13.3(chr16:46766-4247185)x3 copy number gain See cases [RCV000136687] Chr16:46766..4247185 [GRCh38]
Chr16:96766..4297186 [GRCh37]
Chr16:36766..4237187 [NCBI36]
Chr16:16p13.3
pathogenic
GRCh38/hg38 16p13.3-13.12(chr16:43732-13326806)x3 copy number gain See cases [RCV000139166] Chr16:43732..13326806 [GRCh38]
Chr16:93732..13420663 [GRCh37]
Chr16:33732..13328164 [NCBI36]
Chr16:16p13.3-13.12
pathogenic
GRCh38/hg38 16p13.3-13.11(chr16:666662-15743104)x3 copy number gain See cases [RCV000143710] Chr16:666662..15743104 [GRCh38]
Chr16:716662..15836961 [GRCh37]
Chr16:656663..15744462 [NCBI36]
Chr16:16p13.3-13.11
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:102839-28327676)x3 copy number gain See cases [RCV000203445] Chr16:102839..28327676 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3 copy number gain Ductal breast carcinoma [RCV000207053] Chr16:1279324..31926800 [GRCh37]
Chr16:16p13.3-11.2
uncertain significance
GRCh37/hg19 16p13.3-12.3(chr16:1274615-19073133)x3 copy number gain Ductal breast carcinoma [RCV000207326] Chr16:1274615..19073133 [GRCh37]
Chr16:16p13.3-12.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:1860861-2070554)x3 copy number gain See cases [RCV000240428] Chr16:1860861..2070554 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:78801-9169448) copy number gain See cases [RCV000446555] Chr16:78801..9169448 [GRCh37]
Chr16:16p13.3-13.2
pathogenic
GRCh37/hg19 16p13.3(chr16:97133-5122974)x3 copy number gain See cases [RCV000445663] Chr16:97133..5122974 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:643377-3125125)x3 copy number gain See cases [RCV000510815] Chr16:643377..3125125 [GRCh37]
Chr16:16p13.3
uncertain significance
maternal UPD(16p) complex Hemimegalencephaly [RCV000494707] Chr16:1280042..33710558 [GRCh37]
Chr16:16p13.3-11.2
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-13.2(chr16:85880-9883129)x3 copy number gain See cases [RCV000510698] Chr16:85880..9883129 [GRCh37]
Chr16:16p13.3-13.2
pathogenic
GRCh37/hg19 16p13.3-12.2(chr16:85880-22442007)x3 copy number gain See cases [RCV000511360] Chr16:85880..22442007 [GRCh37]
Chr16:16p13.3-12.2
pathogenic
GRCh37/hg19 16p13.3-12.3(chr16:85880-19806921)x3 copy number gain See cases [RCV000512194] Chr16:85880..19806921 [GRCh37]
Chr16:16p13.3-12.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3(chr16:85880-3216551)x3 copy number gain not provided [RCV000683742] Chr16:85880..3216551 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1734363-2285561)x1 copy number loss not provided [RCV000683746] Chr16:1734363..2285561 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1505184-4415346)x3 copy number gain not provided [RCV000683745] Chr16:1505184..4415346 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3-13.13(chr16:85880-11209288)x3 copy number gain not provided [RCV000683743] Chr16:85880..11209288 [GRCh37]
Chr16:16p13.3-13.13
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3
pathogenic
GRCh37/hg19 16p13.3(chr16:1807896-2311160)x3 copy number gain not provided [RCV000738986] Chr16:1807896..2311160 [GRCh37]
Chr16:16p13.3
benign
GRCh37/hg19 16p13.3(chr16:1813658-2319717)x3 copy number gain not provided [RCV000738989] Chr16:1813658..2319717 [GRCh37]
Chr16:16p13.3
benign
NM_002952.4(RPS2):c.255C>T (p.Ser85=) single nucleotide variant not provided [RCV000962383] Chr16:1964288 [GRCh38]
Chr16:2014289 [GRCh37]
Chr16:16p13.3
benign
NM_002952.4(RPS2):c.138A>G (p.Arg46=) single nucleotide variant not provided [RCV000947660] Chr16:1964488 [GRCh38]
Chr16:2014489 [GRCh37]
Chr16:16p13.3
benign
NC_000016.10:g.(?_1523498)_(2064447_?)del deletion Tuberous sclerosis 2 [RCV001032344] Chr16:1573499..2114448 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2148005_?)del deletion Tuberous sclerosis 2 [RCV001033183] Chr16:624055..2148005 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:109978-4316797) copy number gain Chromosome 16p13.3 duplication syndrome [RCV000767731] Chr16:109978..4316797 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2115656_?)del deletion Tuberous sclerosis 2 [RCV000811345] Chr16:624055..2115656 [GRCh37]
Chr16:16p13.3
pathogenic
GRCh37/hg19 16p13.3(chr16:85880-2053328)x1 copy number loss not provided [RCV000849039] Chr16:85880..2053328 [GRCh37]
Chr16:16p13.3
pathogenic
Single allele inversion Hereditary cancer-predisposing syndrome [RCV000850149] Chr16:1566500..2119769 [GRCh37]
Chr16:16p13.3
uncertain significance
NC_000016.9:g.(?_1203718)_(2185710_?)del deletion Tuberous sclerosis 2 [RCV001033886] Chr16:1203718..2185710 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2550979_?)dup duplication Idiopathic generalized epilepsy [RCV001033790] Chr16:624055..2550979 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:2011148-2161281)x3 copy number gain not provided [RCV001259758] Chr16:2011148..2161281 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:85880-5249457)x3 copy number gain not provided [RCV001259749] Chr16:85880..5249457 [GRCh37]
Chr16:16p13.3
pathogenic
NC_000016.9:g.(?_624055)_(2153916_?)dup duplication Epilepsy [RCV001344085]|Idiopathic generalized epilepsy [RCV001316565] Chr16:624055..2153916 [GRCh37]
Chr16:16p13.3
uncertain significance
GRCh37/hg19 16p13.3(chr16:84485-5251013)x3 copy number gain not provided [RCV001537890] Chr16:84485..5251013 [GRCh37]
Chr16:16p13.3
pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:10404 AgrOrtholog
COSMIC RPS2 COSMIC
Ensembl Genes ENSG00000140988 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000341885 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000433034 UniProtKB/TrEMBL
  ENSP00000433170 UniProtKB/TrEMBL
  ENSP00000434846 UniProtKB/TrEMBL
  ENSP00000436227 UniProtKB/TrEMBL
  ENSP00000436356 UniProtKB/TrEMBL
  ENSP00000436865 UniProtKB/TrEMBL
  ENSP00000454837 UniProtKB/TrEMBL
  ENSP00000460860 UniProtKB/TrEMBL
Ensembl Transcript ENST00000343262 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000526522 UniProtKB/TrEMBL
  ENST00000526586 UniProtKB/TrEMBL
  ENST00000527302 UniProtKB/TrEMBL
  ENST00000529806 UniProtKB/TrEMBL
  ENST00000530225 UniProtKB/TrEMBL
  ENST00000532746 UniProtKB/TrEMBL
  ENST00000533186 UniProtKB/TrEMBL
  ENST00000563194 UniProtKB/TrEMBL
Gene3D-CATH 3.30.230.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000140988 GTEx
HGNC ID HGNC:10404 ENTREZGENE
Human Proteome Map RPS2 Human Proteome Map
InterPro Ribosomal_S5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_D2-typ_fold UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_D2-typ_fold_subgr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_euk/arc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_N_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:6187 UniProtKB/Swiss-Prot
NCBI Gene 6187 ENTREZGENE
OMIM 603624 OMIM
PANTHER PTHR13718 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Ribosomal_S5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S5_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA34806 PharmGKB
PROSITE RIBOSOMAL_S5 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  S5_DSRBD UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF54211 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
TIGRFAMs uS5_euk_arch UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt D3DU83_HUMAN UniProtKB/TrEMBL
  E9PM36_HUMAN UniProtKB/TrEMBL
  E9PMM9_HUMAN UniProtKB/TrEMBL
  E9PPT0_HUMAN UniProtKB/TrEMBL
  E9PQD7_HUMAN UniProtKB/TrEMBL
  H0YE27_HUMAN UniProtKB/TrEMBL
  H0YEN5_HUMAN UniProtKB/TrEMBL
  H3BNG3_HUMAN UniProtKB/TrEMBL
  I3L404_HUMAN UniProtKB/TrEMBL
  P15880 ENTREZGENE
  Q3KQT6_HUMAN UniProtKB/TrEMBL
  Q6IPX5_HUMAN UniProtKB/TrEMBL
  Q8J014_HUMAN UniProtKB/TrEMBL
  Q8N5L9_HUMAN UniProtKB/TrEMBL
  Q9BSW5_HUMAN UniProtKB/TrEMBL
  RS2_HUMAN UniProtKB/Swiss-Prot
UniProt Secondary B2R5G0 UniProtKB/Swiss-Prot
  D3DU82 UniProtKB/Swiss-Prot
  Q3MIB1 UniProtKB/Swiss-Prot