{
    "uniprot_canonical_ac": "P14206-1",
    "uniprot_ac": "P14206",
    "uniprot_id": "RSSA_MOUSE",
    "mass": {
        "chemical_mass": 32838.0,
        "monoisotopic_mass": 32838.0
    },
    "refseq": {
        "ac": "NP_035159",
        "name": "small ribosomal subunit protein uS2",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159"
    },
    "gene_names": [
        {
            "name": "Rpsa",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P14206",
            "id": "P14206"
        },
        {
            "name": "67kDa; 67lr; Lamr; Lamr1; Lamrl1; MLR; P40; P40-3; P40-8",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159",
            "id": "NP_035159"
        },
        {
            "name": "Lamr1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P14206",
            "id": "P14206"
        },
        {
            "name": "P40-8",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P14206",
            "id": "P14206"
        },
        {
            "name": "Rpsa",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159",
            "id": "NP_035159"
        }
    ],
    "protein_names": [
        {
            "name": "Small ribosomal subunit protein uS2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "37 kDa laminin receptor precursor",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "37 kDa oncofetal antigen",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "37/67 kDa laminin receptor",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "37LRP",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "40S ribosomal protein SA; 37LRP; LRP/LR; LBP/p40; OFA/iLRP; 67 kDa laminin receptor; 37 kDa oncofetal antigen; 37/67 kDa laminin receptor; 37 kDa laminin receptor; laminin-binding protein precursor p40; P40-3, functional; P40-8, functional; laminin receptor 1 (67kD, ribosomal protein SA); 67LR",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159",
            "id": "NP_035159"
        },
        {
            "name": "40S ribosomal protein SA",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "67 kDa laminin receptor",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "67LR",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "LBP/p40",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "LRP/LR",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "LamR",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "Laminin receptor 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "Laminin-binding protein precursor p40",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "OFA/iLRP",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P14206"
        },
        {
            "name": "small ribosomal subunit protein uS2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159",
            "id": "NP_035159"
        }
    ],
    "function": [
        {
            "annotation": "High 67-kDa laminin receptor expression is associated with obesity-induced inflammation.",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_035159",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_035159"
                },
                {
                    "database": "PubMed",
                    "id": "28154178",
                    "url": "https://glygen.org/publication/PubMed/28154178"
                }
            ]
        },
        {
            "annotation": "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 receptor for laminin. Plays a role in cell adhesion to the basement membrane and in the consequent activation of signaling transduction pathways. May play a role in cell fate determination and tissue morphogenesis. Also acts as a receptor for several other ligands, including the pathogenic prion protein, viruses, and bacteria. Acts as a PPP1R16B-dependent substrate of PPP1CA (By similarity). Enables malignant tumor cells to penetrate laminin tissue and vessel barriers. Activates precursor thymic anti-OFA/iLRP specific cytotoxic T-cell. May induce CD8 T-suppressor cells secreting IL-10.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P14206",
                    "url": "https://www.uniprot.org/uniprot/P14206#function"
                },
                {
                    "database": "PubMed",
                    "id": "1374897",
                    "url": "https://glygen.org/publication/PubMed/1374897"
                },
                {
                    "database": "PubMed",
                    "id": "10697612",
                    "url": "https://glygen.org/publication/PubMed/10697612"
                },
                {
                    "database": "PubMed",
                    "id": "6302102",
                    "url": "https://glygen.org/publication/PubMed/6302102"
                },
                {
                    "database": "UniProtKB",
                    "id": "MF_03016",
                    "url": "https://www.uniprot.org/uniprot/MF_03016#function"
                },
                {
                    "database": "PubMed",
                    "id": "6301485",
                    "url": "https://glygen.org/publication/PubMed/6301485"
                },
                {
                    "database": "PubMed",
                    "id": "16453457",
                    "url": "https://glygen.org/publication/PubMed/16453457"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0110074",
            "recommended_name": {
                "id": "DOID:0110074",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110074",
                "name": "arrhythmogenic right ventricular dysplasia 5",
                "description": "An arrhythmogenic right ventricular dysplasia that has_material_basis_in heterozygous mutation in the TMEM43 gene on chromosome 3p25."
            },
            "synonyms": [
                {
                    "id": "DOID:0110074",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110074",
                    "name": "ARVC5",
                    "description": ""
                },
                {
                    "id": "DOID:0110074",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110074",
                    "name": "ARVD5",
                    "description": ""
                },
                {
                    "id": "DOID:0110074",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110074",
                    "name": "arrhythmogenic right ventricular cardiomyopathy 5",
                    "description": ""
                },
                {
                    "id": "DOID:0110074",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110074",
                    "name": "familial arrhythmogenic right ventricular dysplasia 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular dysplasia 5",
                    "description": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the TMEM43 gene."
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "ARVC5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "ARVD5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "TMEM43 arrhythmogenic right ventricular cardiomyopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular cardiomyopathy 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TMEM43",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular dysplasia 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular dysplasia type 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular dysplasia, familial, type 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "familial arrhythmogenic right ventricular dysplasia 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0011459",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0011459",
                    "name": "arrhythmogenic right ventricular dysplasia, familial, 5",
                    "description": ""
                },
                {
                    "id": "MIM:604400",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/604400",
                    "name": "Arrhythmogenic right ventricular dysplasia, familial, 5",
                    "description": "Arrhythmogenic right ventricular dysplasia, familial, 5"
                }
            ],
            "evidence": [
                {
                    "id": "0110074",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110074"
                }
            ]
        },
        {
            "disease_id": "DOID:11446",
            "recommended_name": {
                "id": "DOID:11446",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11446",
                "name": "sciatic neuropathy",
                "description": ""
            },
            "synonyms": [],
            "evidence": [
                {
                    "id": "11446",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:11446"
                }
            ]
        },
        {
            "disease_id": "DOID:1339",
            "recommended_name": {
                "id": "DOID:1339",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1339",
                "name": "Diamond-Blackfan anemia",
                "description": "A congenital hypoplastic anemia that is characterized by anemia (low red blood cell counts) with decreased erythroid progenitors in the bone marrow and has_material_basis_insufficient levels of red blood cells due to bone marrow dysfunction."
            },
            "synonyms": [
                {
                    "id": "DOID:1339",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1339",
                    "name": "Blackfan - Diamond syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:1339",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1339",
                    "name": "chronic constitutional pure red cell anaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan anemia 1",
                    "description": "Any Diamond-Blackfan anemia in which the cause of the disease is a mutation in the RPS19 gene."
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "DBA",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan Anaemia type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan Anemia type 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan anaemia caused by mutation in RPS19",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan anemia 1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Diamond-Blackfan anemia caused by mutation in RPS19",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "RPS19 Diamond-Blackfan anaemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "RPS19 Diamond-Blackfan anemia",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Aase syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Aase-Smith syndrome 2",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Blackfan-Diamond syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "DBA1",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "Red cell aplasia, Pure, hereditary",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "anemia, congenital erythroid hypoplastic",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "anemia, congenital hypoplastic, of Blackfan and Diamond",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "aregenerative Anemia, chronic congenital",
                    "description": ""
                },
                {
                    "id": "MONDO:0007110",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007110",
                    "name": "erythrogenesis imperfecta",
                    "description": ""
                },
                {
                    "id": "MIM:105650",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/105650",
                    "name": "Diamond-Blackfan anemia 1",
                    "description": "Diamond-Blackfan anemia 1"
                }
            ],
            "evidence": [
                {
                    "id": "1339",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1339"
                }
            ]
        },
        {
            "disease_id": "DOID:9778",
            "recommended_name": {
                "id": "DOID:9778",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:9778",
                "name": "irritable bowel syndrome",
                "description": "An intestinal disease that is characterized by chronic abdominal pain, discomfort, bloating, and alteration of bowel habits in the absence of any detectable organic cause."
            },
            "synonyms": [
                {
                    "id": "DOID:9778",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9778",
                    "name": "IBD",
                    "description": ""
                },
                {
                    "id": "DOID:9778",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:9778",
                    "name": "Irritable colon",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "9778",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:9778"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Mus musculus",
            "taxid": 10090,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P14206",
                    "url": "https://www.uniprot.org/uniprot/P14206"
                }
            ],
            "common_name": "Mouse"
        }
    ],
    "gene": [
        {
            "name": "Rpsa",
            "url": "https://www.uniprot.org/uniprot/P14206",
            "locus": {
                "chromosome": "9",
                "start_pos": 119961435,
                "end_pos": 119956755,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSMUSG00000032518",
                        "url": "https://www.ensembl.org/id/ENSMUSG00000032518"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSMUSG00000032518",
            "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000032518",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd01425",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd01425",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "CHEMBL1075301",
            "url": "https://www.ebi.ac.uk/chembldb/target/inspect/CHEMBL1075301",
            "database": "ChEMBL",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "16785",
            "url": "https://www.ncbi.nlm.nih.gov/gene/16785",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "P14206",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:P14206*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR001865",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001865",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR005707",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR005707",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018130",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018130",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR023591",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR023591",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR027498",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR027498",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR027504",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR027504",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR032281",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR032281",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "mmu:16785",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:16785",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "105381",
            "url": "http://www.informatics.jax.org/marker/MGI:105381",
            "database": "MGI",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "P14206",
            "url": "https://www.oglcnac.mcw.edu/search/?query_protein=P14206",
            "database": "O-GlcNAc Database",
            "categories": [
                "Glycoproteomics"
            ]
        },
        {
            "id": "QKFIEPR",
            "url": "https://omabrowser.org/oma/group/QKFIEPR/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "5480124at2759",
            "url": "http://www.orthodb.org/?query=5480124at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
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                {
                    "id": "36288343",
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        {
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        {
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            "title": "37 kilodalton oncofetal antigen protein and immature laminin receptor protein are identical, universal T-cell inducing immunogens on primary rodent and human cancers.",
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        {
            "title": "Midkine binds to 37-kDa laminin binding protein precursor, leading to nuclear transport of the complex.",
            "journal": "Exp. Cell Res.",
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            "authors": "Kimura T., Muramatsu H., Muramatsu T., Inui T., Zou K., Salama R.H.M.",
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                {
                    "type": "PubMed",
                    "id": "11597123",
                    "url": "https://glygen.org/publication/PubMed/11597123"
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        {
            "title": "The 37-kDa/67-kDa laminin receptor acts as the cell-surface receptor for the cellular prion protein.",
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        {
            "title": "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells.",
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            "title": "Subcellular localization of prion proteins and the 37 kDa/67 kDa laminin receptor fused to fluorescent proteins.",
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            "authors": "Kumazoe M, Nakamura Y, Yamashita M, Suzuki T, Takamatsu K, Huang Y, Bae J, Yamashita S, Murata M, Yamada S, Shinoda Y, Yamaguchi W, Toyoda Y, Tachibana H",
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        {
            "id": "mmu:16785",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:16785",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-MMU-156827",
            "name": "L13a-mediated translational silencing of Ceruloplasmin expression",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-156827",
            "resource": "Reactome",
            "description": "L13a-mediated translational silencing of Ceruloplasmin expression"
        },
        {
            "id": "R-MMU-1799339",
            "name": "SRP-dependent cotranslational protein targeting to membrane",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-1799339",
            "resource": "Reactome",
            "description": "SRP-dependent cotranslational protein targeting to membrane"
        },
        {
            "id": "R-MMU-6791226",
            "name": "Major pathway of rRNA processing in the nucleolus and cytosol",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-6791226",
            "resource": "Reactome",
            "description": "Major pathway of rRNA processing in the nucleolus and cytosol"
        },
        {
            "id": "R-MMU-72649",
            "name": "Translation initiation complex formation",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-72649",
            "resource": "Reactome",
            "description": "Translation initiation complex formation"
        },
        {
            "id": "R-MMU-72689",
            "name": "Formation of a pool of free 40S subunits",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-72689",
            "resource": "Reactome",
            "description": "Formation of a pool of free 40S subunits"
        },
        {
            "id": "R-MMU-72695",
            "name": "Formation of the ternary complex, and subsequently, the 43S complex",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-72695",
            "resource": "Reactome",
            "description": "Formation of the ternary complex, and subsequently, the 43S complex"
        },
        {
            "id": "R-MMU-72702",
            "name": "Ribosomal scanning and start codon recognition",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-72702",
            "resource": "Reactome",
            "description": "Ribosomal scanning and start codon recognition"
        },
        {
            "id": "R-MMU-72706",
            "name": "GTP hydrolysis and joining of the 60S ribosomal subunit",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-72706",
            "resource": "Reactome",
            "description": "GTP hydrolysis and joining of the 60S ribosomal subunit"
        },
        {
            "id": "R-MMU-975956",
            "name": "Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-975956",
            "resource": "Reactome",
            "description": "Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC)"
        },
        {
            "id": "R-MMU-975957",
            "name": "Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)",
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-975957",
            "resource": "Reactome",
            "description": "Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC)"
        }
    ],
    "orthologs": [
        {
            "uniprot_canonical_ac": "P08865-1",
            "protein_name": "Small ribosomal subunit protein uS2",
            "gene_name": "RPSA",
            "tax_id": 9606,
            "organism": "Homo sapiens",
            "sequence": {
                "sequence": "MSGALDVLQMKEEDVLKFLAAGTHLGGTNLDFQMEQYIYKRKSDGIYIINLKRTWEKLLLAARAIVAIENPADVSVISSRNTGQRAVLKFAAATGATPIAGRFTPGTFTNQIQAAFREPRLLVVTDPRADHQPLTEASYVNLPTIALCNTDSPLRYVDIAIPCNNKGAHSVGLMWWMLAREVLRMRGTISREHPWEVMPDLYFYRDPEEIEKEEQAAAEKAVTKEEFQGEWTAPAPEFTATQPEVADWSEGVQVPSVPIQQFPTEDWSAQPATEDWSAAPTAQATEWVGATTDWS",
                "length": 295
            },
            "evidence": [
                {
                    "id": "45226131",
                    "url": "http://www.informatics.jax.org/homology/45226131",
                    "database": "MGI"
                }
            ],
            "common_name": "Human"
        },
        {
            "uniprot_canonical_ac": "P32905-1",
            "protein_name": "Small ribosomal subunit protein uS2A",
            "gene_name": "RPS0A",
            "tax_id": 559292,
            "organism": "Saccharomyces cerevisiae S288C",
            "sequence": {
                "sequence": "MSLPATFDLTPEDAQLLLAANTHLGARNVQVHQEPYVFNARPDGVHVINVGKTWEKLVLAARIIAAIPNPEDVVAISSRTFGQRAVLKFAAHTGATPIAGRFTPGSFTNYITRSFKEPRLVIVTDPRSDAQAIKEASYVNIPVIALTDLDSPSEFVDVAIPCNNRGKHSIGLIWYLLAREVLRLRGALVDRTQPWSIMPDLYFYRDPEEVEQQVAEEATTEEAGEEEAKEEVTEEQAEATEWAEENADNVEW",
                "length": 252
            },
            "evidence": [
                {
                    "id": "P14206",
                    "url": "https://omabrowser.org/oma/group/P14206/",
                    "database": "OMA"
                }
            ],
            "common_name": "Yeast"
        },
        {
            "uniprot_canonical_ac": "P38983-1",
            "protein_name": "Small ribosomal subunit protein uS2",
            "gene_name": "Rpsa",
            "tax_id": 10116,
            "organism": "Rattus norvegicus",
            "sequence": {
                "sequence": "MSGGLDVLQMKEEDVLKFLAAGTHLGGTNLDFQMEQYIYKRKSDGIYIINLKRTWEKLLLAARAIVAIENPADVSVISSRNTGQRAVLKFAAATGATPIAGRFTPGTFTNQIQAAFREPRLLVVTDPRADHQPLTEASYVNLPTIALCNTDSPLRYVDIAIPCNNKGAHSVGLMWWMLAREVLRMRGTISREHPWEVMPDLYFYRDPEEIEKEEQAAAEKAVTKEEFQGEWTAPAPEFTAAQPEVADWSEGVQVPSVPIQQFPTEDWSAQPATEDWSAAPTAQATEWVGATTEWS",
                "length": 295
            },
            "evidence": [
                {
                    "id": "45226131",
                    "url": "http://www.informatics.jax.org/homology/45226131",
                    "database": "MGI"
                }
            ],
            "common_name": "Rat"
        }
    ],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 4,
                "go_terms": [
                    {
                        "name": "translation",
                        "id": "GO:0006412",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006412",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cell-cell adhesion",
                        "id": "GO:0098609",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098609",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytoplasmic translation",
                        "id": "GO:0002181",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0002181",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ribosomal small subunit assembly",
                        "id": "GO:0000028",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0000028",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 15,
                "go_terms": [
                    {
                        "name": "small ribosomal subunit",
                        "id": "GO:0015935",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015935",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "glutamatergic synapse",
                        "id": "GO:0098978",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098978",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "nucleus",
                        "id": "GO:0005634",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytoplasm",
                        "id": "GO:0005737",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosol",
                        "id": "GO:0005829",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "membrane",
                        "id": "GO:0016020",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016020",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neuronal cell body",
                        "id": "GO:0043025",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "synapse",
                        "id": "GO:0045202",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045202",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "postsynapse",
                        "id": "GO:0098794",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098794",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "basement membrane",
                        "id": "GO:0005604",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005604",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ribosome",
                        "id": "GO:0005840",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005840",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosolic ribosome",
                        "id": "GO:0022626",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022626",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cytosolic small ribosomal subunit",
                        "id": "GO:0022627",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0022627",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "collagen-containing extracellular matrix",
                        "id": "GO:0062023",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0062023",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 4,
                "go_terms": [
                    {
                        "name": "structural constituent of ribosome",
                        "id": "GO:0003735",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003735",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "laminin binding",
                        "id": "GO:0043236",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043236",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "ribosome binding",
                        "id": "GO:0043022",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043022",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "laminin receptor activity",
                        "id": "GO:0005055",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005055",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "P14206",
                                "url": "https://www.uniprot.org/uniprot/P14206"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [],
    "ptm_annotation": [
        {
            "annotation": "Acylated. Acylation may be a prerequisite for conversion of the monomeric 37 kDa laminin receptor precursor (37LRP) to the mature dimeric 67 kDa laminin receptor (67LR), and may provide a mechanism for membrane association.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P14206",
                    "url": "https://www.uniprot.org/uniprot/P14206"
                },
                {
                    "database": "PubMed",
                    "id": "MF_03016",
                    "url": "https://glygen.org/publication/PubMed/MF_03016"
                }
            ]
        },
        {
            "annotation": "Cleaved by stromelysin-3 (ST3) at the cell surface. Cleavage by stromelysin-3 may be a mechanism to alter cell-extracellular matrix interactions.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P14206",
                    "url": "https://www.uniprot.org/uniprot/P14206"
                },
                {
                    "database": "PubMed",
                    "id": "MF_03016",
                    "url": "https://glygen.org/publication/PubMed/MF_03016"
                }
            ]
        }
    ],
    "interactions": [],
    "reactions": [],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        },
        {
            "name": "homologset.mgi",
            "label": "MGI Homologs"
        },
        {
            "name": "homologset.oma",
            "label": "OMA Homologs"
        }
    ],
    "section_stats": [
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                    "field": "n_linked_glycan_sites",
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            "sort_fields": []
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        {
            "table_id": "phosphorylation",
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            "sort_fields": [
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        },
        {
            "table_id": "snv",
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        {
            "table_id": "snv_disease",
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                {
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        {
            "table_id": "snv_non_disease",
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            "sort_fields": [
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    ]
}
