Gene Gene information from NCBI Gene database.
Entrez ID 3921
Gene name Ribosomal protein SA
Gene symbol RPSA
Synonyms (NCBI Gene)
37LRP67LRICASLAMBRLAMR1LBPLBP/p40LRPLRP/LRNEM/1CHD4SAlamRp40uS2
Chromosome 3
Chromosome location 3p22.1
Summary Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, n
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs398122389 ->TCATG Pathogenic Coding sequence variant, frameshift variant
miRNA miRNA information provided by mirtarbase database.
27
miRTarBase ID miRNA Experiments Reference
MIRT031978 hsa-miR-16-5p Proteomics 18668040
MIRT052459 hsa-let-7a-5p CLASH 23622248
MIRT051967 hsa-let-7b-5p CLASH 23622248
MIRT051511 hsa-let-7e-5p CLASH 23622248
MIRT051008 hsa-miR-17-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
45
GO ID Ontology Definition Evidence Reference
GO:0000028 Process Ribosomal small subunit assembly IBA
GO:0000028 Process Ribosomal small subunit assembly IEA
GO:0001618 Function Virus receptor activity IEA
GO:0002181 Process Cytoplasmic translation IBA
GO:0002181 Process Cytoplasmic translation IC 23636399
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
150370 6502 ENSG00000168028
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P08865
Protein name Small ribosomal subunit protein uS2 (37 kDa laminin receptor precursor) (37LRP) (37/67 kDa laminin receptor) (LRP/LR) (40S ribosomal protein SA) (67 kDa laminin receptor) (67LR) (Colon carcinoma laminin-binding protein) (Laminin receptor 1) (LamR) (Lamini
Protein function Required for the assembly and/or stability of the 40S ribosomal subunit. Required for the processing of the 20S rRNA-precursor to mature 18S rRNA in a late step of the maturation of 40S ribosomal subunits. Also functions as a cell surface recept
PDB 3BCH , 4UG0 , 4V5Z , 4V6X , 5A2Q , 5AJ0 , 5FLX , 5LKS , 5OA3 , 5T2C , 5VYC , 6FEC , 6G18 , 6G4S , 6G51 , 6G53 , 6G5H , 6G5I , 6IP5 , 6IP6 , 6IP8 , 6OLE , 6OLF , 6OLG , 6OLI , 6OLZ , 6OM0 , 6OM7 , 6QZP , 6XA1 , 6Y0G , 6Y2L , 6Y57 , 6YBD , 6YBW , 6Z6L , 6Z6M , 6Z6N , 6ZLW , 6ZM7 , 6ZME , 6ZMI , 6ZMO , 6ZMT , 6ZMW , 6ZN5 , 6ZOJ , 6ZOK , 6ZON , 6ZP4 , 6ZUO
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00318 Ribosomal_S2 18 118 Ribosomal protein S2 Family
PF00318 Ribosomal_S2 111 184 Ribosomal protein S2 Family
PF16122 40S_SA_C 202 295 40S ribosomal protein SA C-terminus Family
Sequence
Sequence length 295
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Ribosome
Coronavirus disease - COVID-19
  L13a-mediated translational silencing of Ceruloplasmin expression
SRP-dependent cotranslational protein targeting to membrane
Viral mRNA Translation
Major pathway of rRNA processing in the nucleolus and cytosol
Translation initiation complex formation
Formation of a pool of free 40S subunits
Formation of the ternary complex, and subsequently, the 43S complex
Ribosomal scanning and start codon recognition
GTP hydrolysis and joining of the 60S ribosomal subunit
Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)
Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
21
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial isolated congenital asplenia Pathogenic; Likely pathogenic rs397514759, rs398122389, rs397514760, rs397514761, rs397514762, rs397514763 RCV000054822
RCV000054823
RCV000054824
RCV000054825
RCV000054826
RCV000054827
RCV000054828
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial cancer of breast Likely benign rs62242645 RCV005934809
Malignant tumor of esophagus Likely benign rs62242645 RCV005934810
RPSA-related disorder Uncertain significance; Likely benign; Benign rs758186843, rs190008375, rs369708612, rs529221890 RCV003953943
RCV004756408
RCV003427961
RCV003918602
Thymoma Likely benign rs62242645 RCV005934811
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 1443045
Alzheimer Disease Associate 24048171, 24048412, 35766008, 40037473
Angiodysplasia Associate 31498527
Arthritis Rheumatoid Inhibit 30718719
Bone Marrow Diseases Associate 7911032
Breast Neoplasms Associate 26427016, 26545108
Carcinogenesis Associate 40141206
Carcinoma Hepatocellular Associate 32964027
Cerebral Infarction Associate 40696650
Classical Lissencephalies and Subcortical Band Heterotopias Associate 34347028