RPSA2 (ribosomal protein SA 2) - Rat Genome Database

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Gene: RPSA2 (ribosomal protein SA 2) Homo sapiens
Analyze
No known orthologs.
Symbol: RPSA2
Name: ribosomal protein SA 2
RGD ID: 1601794
HGNC Page HGNC:36809
Description: Predicted to enable laminin binding activity and laminin receptor activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in cell adhesion; cytoplasmic translation; and ribosomal small subunit assembly. Predicted to be located in several cellular components, including nucleus; plasma membrane; and ribosome. Predicted to be part of 90S preribosome and cytosolic small ribosomal subunit; INTERACTS WITH 2-hydroxypropanoic acid; all-trans-retinoic acid; aristolochic acid A.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 37 kDa laminin receptor; 37/67 kDa laminin receptor; 37LRP; 40S ribosomal protein SA; 40S ribosomal protein SA2; 67 kDa laminin receptor; 67LR; laminin receptor 1; laminin-binding protein precursor p40; LamR; LBP/p40; LRP/LR; ribosomal protein SA pseudogene; ribosomal protein SA pseudogene 58; RPSA_30_1642; RPSAP58; similar to laminin receptor 1; small ribosomal subunit protein uS2B
RGD Orthologs
Alliance Genes
More Info homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381923,758,496 - 23,871,188 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1923,762,944 - 23,871,162 (+)EnsemblGRCh38hg38GRCh38
GRCh371923,941,298 - 24,053,990 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361923,737,656 - 23,802,777NCBINCBI36Build 36hg18NCBI36
Cytogenetic Map19p12NCBI
HuRef1923,490,113 - 23,555,111 (+)NCBIHuRef
CHM1_11923,945,583 - 24,010,419 (+)NCBICHM1_1
T2T-CHM13v2.01923,898,911 - 24,016,747 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
amenorrhea  (IAGP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:19123937   PMID:24999758   PMID:25963833   PMID:26186194   PMID:26990986   PMID:28514442   PMID:28611215   PMID:29228324   PMID:31091453   PMID:33961781   PMID:36373674  


Genomics

Variants

.
Variants in RPSA2
8 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p12(chr19:23442005-23860325)x1 copy number loss See cases [RCV000134824] Chr19:23442005..23860325 [GRCh38]
Chr19:23624807..24043127 [GRCh37]
Chr19:23416647..23834967 [NCBI36]
Chr19:19p12		 benign|likely benign|conflicting data from submitters
GRCh38/hg38 19p12(chr19:23441926-23950272)x3 copy number gain See cases [RCV000135559] Chr19:23441926..23950272 [GRCh38]
Chr19:23624728..24133074 [GRCh37]
Chr19:23416568..23924914 [NCBI36]
Chr19:19p12		 likely benign|uncertain significance
GRCh38/hg38 19p12(chr19:23629461-24183272)x3 copy number gain See cases [RCV000135965] Chr19:23629461..24183272 [GRCh38]
Chr19:23812263..24366074 [GRCh37]
Chr19:23604103..24157914 [NCBI36]
Chr19:19p12		 uncertain significance
GRCh38/hg38 19p12(chr19:23441926-23878224)x1 copy number loss See cases [RCV000137551] Chr19:23441926..23878224 [GRCh38]
Chr19:23624728..24061026 [GRCh37]
Chr19:23416568..23852866 [NCBI36]
Chr19:19p12		 uncertain significance|conflicting data from submitters
GRCh38/hg38 19p12(chr19:23665911-24195691)x3 copy number gain See cases [RCV000139046] Chr19:23665911..24195691 [GRCh38]
Chr19:23848713..24378493 [GRCh37]
Chr19:23640553..24170333 [NCBI36]
Chr19:19p12		 conflicting data from submitters
GRCh38/hg38 19p12(chr19:23427660-23950272)x3 copy number gain See cases [RCV000139909] Chr19:23427660..23950272 [GRCh38]
Chr19:23610462..24133074 [GRCh37]
Chr19:23402302..23924914 [NCBI36]
Chr19:19p12		 uncertain significance
GRCh38/hg38 19p12(chr19:23549190-24195691)x3 copy number gain See cases [RCV000141444] Chr19:23549190..24195691 [GRCh38]
Chr19:23731992..24378493 [GRCh37]
Chr19:23523832..24170333 [NCBI36]
Chr19:19p12		 uncertain significance
GRCh38/hg38 19p12-11(chr19:23631687-24322835)x3 copy number gain See cases [RCV000141725] Chr19:23631687..24322835 [GRCh38]
Chr19:23814489..24505637 [GRCh37]
Chr19:23606329..24297477 [NCBI36]
Chr19:19p12-11		 uncertain significance
GRCh38/hg38 19p12-11(chr19:23540844-24322835)x3 copy number gain See cases [RCV000141938] Chr19:23540844..24322835 [GRCh38]
Chr19:23723646..24505637 [GRCh37]
Chr19:23515486..24297477 [NCBI36]
Chr19:19p12-11		 uncertain significance
GRCh38/hg38 19p12(chr19:23441726-24128733)x1 copy number loss See cases [RCV000142542] Chr19:23441726..24128733 [GRCh38]
Chr19:23624528..24311535 [GRCh37]
Chr19:23416368..24103375 [NCBI36]
Chr19:19p12		 benign
GRCh38/hg38 19p12-11(chr19:23631687-24324339)x4 copy number gain See cases [RCV000143566] Chr19:23631687..24324339 [GRCh38]
Chr19:23814489..24507141 [GRCh37]
Chr19:23606329..24298981 [NCBI36]
Chr19:19p12-11		 uncertain significance
GRCh38/hg38 19p12(chr19:23438627-23899197)x1 copy number loss See cases [RCV000143639] Chr19:23438627..23899197 [GRCh38]
Chr19:23621429..24081999 [GRCh37]
Chr19:23413269..23873839 [NCBI36]
Chr19:19p12		 uncertain significance
GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3 copy number gain See cases [RCV000050635] Chr19:17176767..34924150 [GRCh38]
Chr19:17287576..35415054 [GRCh37]
Chr19:17148576..40106894 [NCBI36]
Chr19:19p13.11-q13.11		 pathogenic
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3 copy number gain See cases [RCV000052912] Chr19:13974677..27839676 [GRCh38]
Chr19:14085489..28330584 [GRCh37]
Chr19:13946489..33022424 [NCBI36]
Chr19:19p13.12-q11		 pathogenic
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19p12(chr19:23685651-24193591)x3 copy number gain See cases [RCV000134965] Chr19:23685651..24193591 [GRCh38]
Chr19:23868453..24376393 [GRCh37]
Chr19:23660293..24168233 [NCBI36]
Chr19:19p12		 pathogenic|uncertain significance
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3 copy number gain See cases [RCV000136696] Chr19:15133594..24193591 [GRCh38]
Chr19:15244405..24376393 [GRCh37]
Chr19:15105405..24168233 [NCBI36]
Chr19:19p13.12-12		 pathogenic|likely pathogenic
NC_000019.9:g.23624728_24054225del429498 deletion Primary amenorrhea [RCV000754468] Chr19:23441926..23871423 [GRCh38]
Chr19:23624728..24054225 [GRCh37]
Chr19:19p12		 likely benign
NM_001355283.3(RPSA2):c.774T>A (p.Pro258=) single nucleotide variant not provided [RCV003425083] Chr19:23827935 [GRCh38]
Chr19:24010737 [GRCh37]
Chr19:19p12		 likely benign
NM_001355283.3(RPSA2):c.702C>T (p.Pro234=) single nucleotide variant not provided [RCV003425082] Chr19:23827863 [GRCh38]
Chr19:24010665 [GRCh37]
Chr19:19p12		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:423
Count of miRNA genes:331
Interacting mature miRNAs:343
Transcripts:ENST00000354585, ENST00000462186, ENST00000486528, ENST00000496398
Prediction methods: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.

Markers in Region
G18061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371923,963,576 - 23,963,790UniSTSGRCh37
Build 361923,755,416 - 23,755,630RGDNCBI36
Celera1923,802,985 - 23,803,199RGD
Cytogenetic Map19p12UniSTS
HuRef1923,508,013 - 23,508,227UniSTS
RH68576  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371923,983,714 - 23,983,935UniSTSGRCh37
GRCh371924,282,914 - 24,283,133UniSTSGRCh37
Build 361923,775,554 - 23,775,775RGDNCBI36
Celera1923,823,070 - 23,823,291RGD
Celera1924,129,681 - 24,129,900UniSTS
Cytogenetic Map19p12UniSTS
HuRef1923,528,149 - 23,528,370UniSTS
HuRef1923,837,219 - 23,837,438UniSTS
D3S3955  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map1p21.1UniSTS
Cytogenetic MapXq21.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map3p22.2UniSTS


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 adipose tissue appendage entire extraembryonic component
High
Medium 1374 1601 903 193 1038 101 2827 1096 2005 79 822 901 92 798 1888
Low 849 1360 545 219 522 149 1230 1026 1573 94 362 383 70 406 898
Below cutoff 53 11 85 50 83 52 122 32 55 128 102 117 2 2

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001355283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001355287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387845 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001387846 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149351 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_149352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170708 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170709 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170710 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170711 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170712 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_170714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC139769 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC071971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF454885 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF454888 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF454894 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459808 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459809 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459810 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459811 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459812 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459813 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459814 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459815 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459817 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459818 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459819 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459820 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459823 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459825 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459826 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459827 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459829 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459830 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459832 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF459833 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495824 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF495993 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  OA986985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000462186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,782,081 - 23,809,515 (+)Ensembl
RefSeq Acc Id: ENST00000471224
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,944 - 23,832,196 (+)Ensembl
RefSeq Acc Id: ENST00000475499
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,951 - 23,835,146 (+)Ensembl
RefSeq Acc Id: ENST00000484897
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,763,004 - 23,828,868 (+)Ensembl
RefSeq Acc Id: ENST00000685013
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,763,011 - 23,787,459 (+)Ensembl
RefSeq Acc Id: ENST00000685490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,775,973 - 23,831,879 (+)Ensembl
RefSeq Acc Id: ENST00000686829
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,956 - 23,871,144 (+)Ensembl
RefSeq Acc Id: ENST00000687994
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,763,004 - 23,870,690 (+)Ensembl
RefSeq Acc Id: ENST00000688405
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,995 - 23,809,513 (+)Ensembl
RefSeq Acc Id: ENST00000689525
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,979 - 23,835,115 (+)Ensembl
RefSeq Acc Id: ENST00000691397
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,985 - 23,871,137 (+)Ensembl
RefSeq Acc Id: ENST00000692590
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,948 - 23,871,162 (+)Ensembl
RefSeq Acc Id: ENST00000692739
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1923,762,995 - 23,785,444 (+)Ensembl
RefSeq Acc Id: NM_001355283   ⟹   NP_001342212
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,828,868 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,970,913 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001355287   ⟹   NP_001342216
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,828,868 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,970,913 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387845   ⟹   NP_001374774
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,828,868 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,970,913 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001387846   ⟹   NP_001374775
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,828,868 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,970,913 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149350
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149351
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_149352
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170708
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170709
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170710
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,835,213 (+)NCBI
T2T-CHM13v2.01923,903,473 - 23,977,264 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170711
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,871,188 (+)NCBI
T2T-CHM13v2.01923,903,473 - 24,016,747 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170712
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,871,188 (+)NCBI
T2T-CHM13v2.01923,903,473 - 24,016,747 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170713
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,763,004 - 23,871,188 (+)NCBI
T2T-CHM13v2.01923,903,473 - 24,016,747 (+)NCBI
Sequence:
RefSeq Acc Id: NR_170714
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381923,758,496 - 23,871,188 (+)NCBI
T2T-CHM13v2.01923,898,911 - 24,016,747 (+)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001342216   ⟸   NM_001355287
- UniProtKB: A0A8I5KQE6 (UniProtKB/TrEMBL),   Q96RS2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001342212   ⟸   NM_001355283
- UniProtKB: A0A8I5KQE6 (UniProtKB/TrEMBL),   Q96RS2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001374774   ⟸   NM_001387845
- UniProtKB: A0A8I5KQE6 (UniProtKB/TrEMBL),   Q96RS2 (UniProtKB/TrEMBL)
RefSeq Acc Id: NP_001374775   ⟸   NM_001387846
- UniProtKB: A0A8I5KQE6 (UniProtKB/TrEMBL),   Q96RS2 (UniProtKB/TrEMBL)
Protein Domains
Small ribosomal subunit protein uS2 C-terminal

Promoters
RGD ID:6796006
Promoter ID:HG_KWN:29472
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   K562,   Lymphoblastoid
Transcripts:NR_003662
Position:
Human AssemblyChrPosition (strand)Source
Build 361923,737,434 - 23,737,934 (+)MPROMDB

Additional Information

Database Acc Id Source(s)
COSMIC RPSA2 COSMIC
Ensembl Genes ENSG00000225178 Ensembl
  ENSG00000288920 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000475499 ENTREZGENE
  ENST00000484897 ENTREZGENE
  ENST00000484897.4 UniProtKB/Swiss-Prot
  ENST00000689525 ENTREZGENE
  ENST00000692590 ENTREZGENE
GTEx ENSG00000225178 GTEx
  ENSG00000288920 GTEx
HGNC ID HGNC:36809 ENTREZGENE
Human Proteome Map RPSA2 Human Proteome Map
InterPro 40S_ribosomal_SA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  40S_SA_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2_euk UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2_euk/arc UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2_flav_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 388524 ENTREZGENE
PANTHER 40S RIBOSOMAL PROTEIN SA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  40S RIBOSOMAL PROTEIN SA-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 40S_SA_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Ribosomal_S2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS RIBOSOMALS2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE RIBOSOMAL_S2_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RIBOSOMAL_S2_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Ribosomal protein S2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A8I5KQE6 ENTREZGENE
  Q96RS2 ENTREZGENE, UniProtKB/TrEMBL
  RPSA2_HUMAN UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2022-09-26 RPSA2  ribosomal protein SA 2  RPSAP58  ribosomal protein SA pseudogene 58  Symbol and/or name change 19259463 PROVISIONAL