{
    "uniprot_canonical_ac": "P12672-1",
    "uniprot_ac": "P12672",
    "uniprot_id": "RAPSN_MOUSE",
    "mass": {
        "chemical_mass": 46393.0,
        "monoisotopic_mass": 46393.0
    },
    "refseq": {
        "ac": "NP_033049",
        "name": "43 kDa receptor-associated protein of the synapse isoform a",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049"
    },
    "gene_names": [
        {
            "name": "Rapsn",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P12672",
            "id": "P12672"
        },
        {
            "name": "43kDa; Nraps; Raps; rapsyn",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049",
            "id": "NP_033049"
        },
        {
            "name": "Rapsn",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049",
            "id": "NP_033049"
        }
    ],
    "protein_names": [
        {
            "name": "43 kDa receptor-associated protein of the synapse",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P12672"
        },
        {
            "name": "43 kDa postsynaptic protein",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P12672"
        },
        {
            "name": "43 kDa receptor-associated protein of the synapse isoform a",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049",
            "id": "NP_033049"
        },
        {
            "name": "43 kDa receptor-associated protein of the synapse; 43 kDa postsynaptic protein; acetylcholine receptor-associated 43 kDa protein; 43kDa acetylcholine receptor-associated protein; receptor-associated protein of the synapse, 43 kDa",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049",
            "id": "NP_033049"
        },
        {
            "name": "Acetylcholine receptor-associated 43 kDa protein",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P12672"
        },
        {
            "name": "RAPsyn",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P12672"
        }
    ],
    "function": [
        {
            "annotation": "Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation. Erratum:[Neuron. 2022 Jan 19;110(2):350. PMID: 35051365]",
            "evidence": [
                {
                    "database": "RefSeq",
                    "id": "NP_033049",
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049"
                },
                {
                    "database": "PubMed",
                    "id": "34033754",
                    "url": "https://glygen.org/publication/PubMed/34033754"
                }
            ]
        },
        {
            "annotation": "Postsynaptic protein required for clustering of nicotinic acetylcholine receptors (nAChRs) at the neuromuscular junction. It may link the receptor to the underlying postsynaptic cytoskeleton, possibly by direct association with actin or spectrin (By similarity).",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P12672",
                    "url": "https://www.uniprot.org/uniprot/P12672#function"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0110675",
            "recommended_name": {
                "id": "DOID:0110675",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0110675",
                "name": "congenital myasthenic syndrome 11",
                "description": "A congenital myasthenic syndrome characterized by autosomal recessive inheritance of low amplitude of the miniature endplate potential and current resulting from deficiency of Acetylcholine Receptor (AChR) at the endplate that has_material_basis_in homozygous or compound heterozygous mutation in the RAPSN gene on chromosome 11p11."
            },
            "synonyms": [
                {
                    "id": "DOID:0110675",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110675",
                    "name": "CMS Ie",
                    "description": ""
                },
                {
                    "id": "DOID:0110675",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110675",
                    "name": "CMS11",
                    "description": ""
                },
                {
                    "id": "DOID:0110675",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110675",
                    "name": "CMS1E",
                    "description": ""
                },
                {
                    "id": "DOID:0110675",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110675",
                    "name": "congenital myasthenic syndrome 1e",
                    "description": ""
                },
                {
                    "id": "DOID:0110675",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0110675",
                    "name": "congenital myasthenic syndrome 11 associated with acetylcholine receptor deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "congenital myasthenic syndrome 11",
                    "description": "Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the RAPSN gene."
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "CMS Ie",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "CMS11",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "CMS1E",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "RAPSN congenital myasthenic syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "congenital myasthenic syndrome 11 associated with acetylcholine receptor deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "congenital myasthenic syndrome 1e",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "congenital myasthenic syndrome caused by mutation in RAPSN",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "congenital myasthenic syndrome type 11",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "Cms Ie",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "Cms Ie, formerly",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "myasthenic syndrome, congenital, Ie",
                    "description": ""
                },
                {
                    "id": "MONDO:0014588",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014588",
                    "name": "myasthenic syndrome, congenital, Ie, formerly",
                    "description": ""
                },
                {
                    "id": "MIM:616326",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/616326",
                    "name": "Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency",
                    "description": "Myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency"
                }
            ],
            "evidence": [
                {
                    "id": "0110675",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0110675"
                }
            ]
        },
        {
            "disease_id": "DOID:0111378",
            "recommended_name": {
                "id": "DOID:0111378",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111378",
                "name": "fetal akinesia deformation sequence syndrome 2",
                "description": "A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the RAPSN gene on chromosome 11p11.2."
            },
            "synonyms": [
                {
                    "id": "DOID:0111378",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111378",
                    "name": "FADS2",
                    "description": ""
                },
                {
                    "id": "MONDO:0100102",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100102",
                    "name": "fetal akinesia deformation sequence 2",
                    "description": "Any fetal akinesia deformation sequence in which the cause of the disease is a mutation in the RAPSN gene."
                },
                {
                    "id": "MONDO:0100102",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0100102",
                    "name": "FADS2",
                    "description": ""
                },
                {
                    "id": "MIM:618388",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/618388",
                    "name": "Fetal akinesia deformation sequence 2",
                    "description": "Fetal akinesia deformation sequence 2"
                }
            ],
            "evidence": [
                {
                    "id": "0111378",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111378"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Mus musculus",
            "taxid": 10090,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P12672",
                    "url": "https://www.uniprot.org/uniprot/P12672"
                }
            ],
            "common_name": "Mouse"
        }
    ],
    "gene": [
        {
            "name": "Rapsn",
            "url": "https://www.uniprot.org/uniprot/P12672",
            "locus": {
                "chromosome": "2",
                "start_pos": 90876074,
                "end_pos": 90865965,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Gene",
                        "id": "ENSMUSG00000002104",
                        "url": "https://www.ensembl.org/id/ENSMUSG00000002104"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "ENSMUSG00000002104",
            "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000002104",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "cd16478",
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd16478",
            "database": "CDD",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "19400",
            "url": "https://www.ncbi.nlm.nih.gov/gene/19400",
            "database": "GeneID",
            "categories": [
                "Genome Annotation"
            ]
        },
        {
            "id": "P12672",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:P12672*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR001237",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001237",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR001841",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR001841",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR011990",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011990",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR013083",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR013083",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018293",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018293",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR019568",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR019568",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR019734",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR019734",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR041617",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR041617",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "mmu:19400",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:19400",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "99422",
            "url": "http://www.informatics.jax.org/marker/MGI:99422",
            "database": "MGI",
            "categories": [
                "Organism-specific"
            ]
        },
        {
            "id": "ALRCSHI",
            "url": "https://omabrowser.org/oma/group/ALRCSHI/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "893642at2759",
            "url": "http://www.orthodb.org/?query=893642at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR46574",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR46574",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR46574:SF1",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR46574:SF1",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF10579",
            "url": "http://pfam.xfam.org/family/PF10579",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13181",
            "url": "http://pfam.xfam.org/family/PF13181",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF13639",
            "url": "http://pfam.xfam.org/family/PF13639",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF17874",
            "url": "http://pfam.xfam.org/family/PF17874",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PR_P12672",
            "url": "http://purl.obolibrary.org/obo/PR_P12672",
            "database": "PRO",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "NP_033049",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_033049",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A2AFX4",
            "url": "https://www.uniprot.org/uniprot/A2AFX4",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A2AFX4-1",
            "url": "https://www.uniprot.org/uniprot/A2AFX4-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A2AFX6",
            "url": "https://www.uniprot.org/uniprot/A2AFX6",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A2AFX6-1",
            "url": "https://www.uniprot.org/uniprot/A2AFX6-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "P12672",
            "url": "https://www.uniprot.org/uniprot/P12672",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "P12672-1",
            "url": "https://www.uniprot.org/uniprot/P12672-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MGQDQTKQQIEKGLQLYQSNQTEKALQVWMKVLEKGSDLVGRFRVLGCLVTAHSEMGRYKEMLKFAVVQIDTARGLEDADFLLESYLNLARSNEKLCEFHKTISYCKTCLGLPGTRAGAQLGGQVSLSMGNAFLGLSLFQKALESFEKALRYAHNNDDTMLECRVCCSLGSFYAQVKDYEKALFFPCKAAELVNDYGKGWSLKYRAMSQYHMAVAYRLLGHLGSAMECCEESMKIALQHGDRPLQALCLLCFADIHRSRGDLETAFPRYDSAMSIMTEIGNRLGQVHVLLGVAKCWMARKVQDKALDAIEKAQDLAEEVGNKLSQLKLHCLSESIYRSKGLQRELRTHVVRFHECVEETELYCGLCGESIGERNSRLQALPCSHIFHLRCLQNNGTRSCPNCRRSSMKPGFV",
        "length": 412,
        "header": "sp|P12672-1|RAPSN_MOUSE Isoform 1 of 43 kDa receptor-associated protein of the synapse  OS=Mus musculus OX=10090 GN=Rapsn PE=2 SV=4 CANONICAL=P12672-1"
    },
    "isoforms": [
        {
            "isoform_ac": "A2AFX4-1",
            "url": "",
            "sequence": {
                "sequence": "MGQDQTKQQIEKGLQLYQSNQTEKALQVWMKVLEKGSDLVGRFRVLGCLVTAHSEMGRYKEMLKFAVVQIDTARGLEDADFLLESYLNLARSNEKLCEFHKTISYCKTCLGLPGTRAGAQLGGQVSLSMGNAFLGLSLFQKALESFEKALRYAHNNDDTMLECRVCCSLGSFYAQVKDYEKALFFPCKAAELVNDYGKGWSLKYRAMSQYHMAVAYRLLGHLGSAMECCEESMKIALQHGDRPLQALCLLCFADIHRSRGDLELSQLKLHCLSESIYRSKGLQRELRTHVVRFHECVEETELYCGLCGESIGERNSRLQALPCSHIFHLRCLQNNGTRSCPNCRRSSMKPGFV",
                "length": 353,
                "header": "tr|A2AFX4-1|A2AFX4_MOUSE Computationally mapped isoform of Receptor-associated protein of the synapse  OS=Mus musculus OX=10090 GN=Rapsn PE=1 SV=1 CANONICAL=P12672-1"
            },
            "locus": {
                "chromosome": "2",
                "start_pos": 90875860,
                "end_pos": 90866142,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSMUST00000111445.10",
                        "url": "https://www.ensembl.org/id/ENSMUST00000111445.10"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSMUSP00000107072.4",
                        "url": "https://www.ensembl.org/id/ENSMUSP00000107072.4"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A2AFX6-1",
            "url": "",
            "sequence": {
                "sequence": "MGQDQTKQQIEKGLQLYQSNQTEKALQVWMKVLEKGSDLVGRFRVLGCLVTAHSEMGRYKEMLKFAVVQIDTARGLEDADFLLESYLNLARSNEKLCEFHKTISYCKTCLGLPGTRAGAQLGGQVSLSMGNAFLGLSLFQKALESFEKALRYAHNNDDTMLECRVCCSLGSFYAQVKESMKIALQHGDRPLQALCLLCFADIHRSRGDLETAFPRYDSAMSIMTEIGNRLGQVHVLLGVAKCWMARKVQDKALDAIEKAQDLAEEVGNKLSQLKLHCLSESIYRSKGLQRELRTHVVRFHECVEETELYCGLCGESIGERNSRLQALPCSHIFHLRCLQNNGTRSCPNCRRSSMKPGFV",
                "length": 359,
                "header": "tr|A2AFX6-1|A2AFX6_MOUSE Computationally mapped isoform of Receptor-associated protein of the synapse  OS=Mus musculus OX=10090 GN=Rapsn PE=1 SV=1 CANONICAL=P12672-1"
            },
            "locus": {
                "chromosome": "2",
                "start_pos": 90875860,
                "end_pos": 90866142,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "ENSMUST00000111446.10",
                        "url": "https://www.ensembl.org/id/ENSMUST00000111446.10"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "ENSMUSP00000107073.4",
                        "url": "https://www.ensembl.org/id/ENSMUSP00000107073.4"
                    }
                ]
            }
        },
        {
            "isoform_ac": "P12672-1",
            "url": "",
            "sequence": {
                "sequence": "MGQDQTKQQIEKGLQLYQSNQTEKALQVWMKVLEKGSDLVGRFRVLGCLVTAHSEMGRYKEMLKFAVVQIDTARGLEDADFLLESYLNLARSNEKLCEFHKTISYCKTCLGLPGTRAGAQLGGQVSLSMGNAFLGLSLFQKALESFEKALRYAHNNDDTMLECRVCCSLGSFYAQVKDYEKALFFPCKAAELVNDYGKGWSLKYRAMSQYHMAVAYRLLGHLGSAMECCEESMKIALQHGDRPLQALCLLCFADIHRSRGDLETAFPRYDSAMSIMTEIGNRLGQVHVLLGVAKCWMARKVQDKALDAIEKAQDLAEEVGNKLSQLKLHCLSESIYRSKGLQRELRTHVVRFHECVEETELYCGLCGESIGERNSRLQALPCSHIFHLRCLQNNGTRSCPNCRRSSMKPGFV",
                "length": 412,
                "header": "sp|P12672-1|RAPSN_MOUSE Isoform 1 of 43 kDa receptor-associated protein of the synapse  OS=Mus musculus OX=10090 GN=Rapsn PE=2 SV=4 CANONICAL=P12672-1"
            },
            "locus": {
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                "start_pos": 90875860,
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                        "id": "ENSMUST00000050323",
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                        "url": "https://www.ensembl.org/id/ENSMUSP00000054150"
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                }
            ],
            "site_lbl": "Tyr86"
        }
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        {
            "title": "Expression of RNA transcripts for the postsynaptic 43 kDa protein in innervated and denervated rat skeletal muscle.",
            "journal": "FEBS Lett.",
            "date": "1989",
            "authors": "Froehner SC",
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                    "url": "https://www.uniprot.org/uniprot/P12672"
                }
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                    "type": "PubMed",
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            ]
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        {
            "title": "A mechanism in agrin signaling revealed by a prevalent Rapsyn mutation in congenital myasthenic syndrome.",
            "journal": "eLife",
            "date": "2019",
            "authors": "Xing G, Jing H, Zhang L, Cao Y, Li L, Zhao K, Dong Z, Chen W, Wang H, Cao R, Xiong WC, Mei L",
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                    "database": "iPTMnet",
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                    "id": "31549961",
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                }
            ]
        },
        {
            "title": "Identification of the mouse muscle 43,000-dalton acetylcholine receptor-associated protein (RAPsyn) by cDNA cloning.",
            "journal": "J. Biol. Chem.",
            "date": "1988",
            "authors": "Frail D.E., Merlie J.P., Mudd J., McLaughlin L.L.",
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                    "database": "UniProtKB",
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                }
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                {
                    "type": "PubMed",
                    "id": "3170600",
                    "url": "https://glygen.org/publication/PubMed/3170600"
                }
            ]
        },
        {
            "title": "Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation.",
            "journal": "Neuron",
            "date": "2021",
            "authors": "Xing G, Jing H, Yu Z, Chen P, Wang H, Xiong WC, Mei L",
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                    "id": "NP_033049",
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                }
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                    "type": "PubMed",
                    "id": "34033754",
                    "url": "https://glygen.org/publication/PubMed/34033754"
                }
            ]
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            "id": "mmu:19400",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:19400",
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        }
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                "length": 412
            },
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                {
                    "id": "45225173",
                    "url": "http://www.informatics.jax.org/homology/45225173",
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                }
            ],
            "common_name": "Rat"
        },
        {
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            {
                "name": "Cellular Component",
                "total": 9,
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                        "name": "cytoplasm",
                        "id": "GO:0005737",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737",
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                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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                            }
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                    {
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                                "id": "P12672",
                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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                        "id": "GO:0031594",
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                                "id": "P12672",
                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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                    {
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                                "id": "P12672",
                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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            {
                "name": "Molecular Function",
                "total": 5,
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                        "name": "acetylcholine receptor binding",
                        "id": "GO:0033130",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033130",
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                                "url": "https://www.uniprot.org/uniprot/P12672"
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                                "id": "P12672",
                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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                        "name": "structural constituent of postsynaptic specialization",
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                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098879",
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                                "database": "UniProtKB",
                                "id": "P12672",
                                "url": "https://www.uniprot.org/uniprot/P12672"
                            }
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                "journal",
                "date",
                "authors"
            ]
        }
    ]
}