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Chem.", "date": "1996", "authors": "Nair S K, Elbaum D, Christianson D W", "reference": { "type": "PubMed", "id": "8557623", "url": "https://pubmed.ncbi.nlm.nih.gov/8557623" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P00918-1", "protein_name": "Carbonic anhydrase 2", "gene_name": "CA2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P00918", "url": "https://www.uniprot.org/uniprotkb/P00918" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.8557623", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": [ { 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"count": 0 }, { "field": "n_linked_glycans", "count": 0 }, { "field": "o_linked_glycans", "count": 0 } ], "sort_fields": [] } ] }, { "title": "BNC1 regulates cell heterogeneity in human pluripotent stem cell-derived epicardium.", "journal": "Development (Cambridge, England)", "date": "2019", "authors": "Gambardella L, McManus SA, Moignard V, Sebukhan D, Delaune A, Andrews S, Bernard WG, Morrison MA, Riley PR, Gottgens B, Gambardella Le Novere N, Sinha S", "reference": { "type": "PubMed", "id": "31767620", "url": "https://pubmed.ncbi.nlm.nih.gov/31767620" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q01954-1", "protein_name": "Zinc finger protein basonuclin-1", "gene_name": "BNC1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q01954", "url": "https://www.uniprot.org/uniprotkb/Q01954" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens 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archives of allergy and immunology", "date": "2021", "authors": "Gao Y, Li J, Jiao J, Li Y, Wang C, Zhang Y, Zhang L", "reference": { "type": "PubMed", "id": "34148047", "url": "https://pubmed.ncbi.nlm.nih.gov/34148047" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "Q01954-1", "protein_name": "Zinc finger protein basonuclin-1", "gene_name": "BNC1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "Q01954", "url": "https://www.uniprot.org/uniprotkb/Q01954" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.34148047", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" 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"Nucleic Acids Res.", "date": "1990", "authors": "Watzele G, Berger E G", "reference": { "type": "PubMed", "id": "2124683", "url": "https://pubmed.ncbi.nlm.nih.gov/2124683" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P15291-1", "protein_name": "Beta-1,4-galactosyltransferase 1", "gene_name": "B4GALT1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P15291", "url": "https://www.uniprot.org/uniprotkb/P15291" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.2124683", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", 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Elena, Mart\u00ednez-Pardo Mercedes, Rold\u00e1n Susana, Tom\u00e1s Miguel, Cabrera Jose C, M\u00e1rtinez-Bugallo Francisco, Mart\u00edn-Viota Luc\u00eda, Vitoria-Mi\u00f1ana Isidro, Lefeber Dirk J, Gir\u00f3s M Luisa, Serrano Gimare Mercedes, Ugarte Magdalena, P\u00e9rez Bel\u00e9n, P\u00e9rez-Cerd\u00e1 Celia", "reference": { "type": "PubMed", "id": "30653653", "url": "https://pubmed.ncbi.nlm.nih.gov/30653653" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P15291-1", "protein_name": "Beta-1,4-galactosyltransferase 1", "gene_name": "B4GALT1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P15291", "url": "https://www.uniprot.org/uniprotkb/P15291" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "snv": [ { "evidence": [ { "id": "rs1840249855", "database": "dbSNP", "url": 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gene on chromosome 9p21.1." }, "synonyms": [ { "id": "DOID:0070256", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070256", "name": "CDG IId", "description": "" }, { "id": "DOID:0070256", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070256", "name": "CDG2D", "description": "" }, { "id": "DOID:0070256", "resource": "Disease Ontology", "url": "https://disease-ontology.org/term/DOID:0070256", "name": "CDGIId", "description": "" }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "B4GALT1-congenital disorder of glycosylation", "description": "B4GALT1-CDG is a congenital disorder of glycosylation characterized by macrocephaly due to Dandy-Walker malformation, hydrocephaly, hypotonia, myopathy and coagulation anomalies. To date, only one case has been reported. The syndrome is associated with mutations in the GALT1 gene (localized to region q13 of chromosome 9) leading to a deficiency in the Golgi apparatus enzyme beta-1,4-galactosyl transferase." }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "B4GALT1-CDG", "description": "" }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "B4GALT1-congenital disorder of glycosylation", "description": "" }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "Beta-1,4-galactosyltransferase deficiency", "description": "" }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "CDG syndrome type IId", "description": "" }, { "id": "MONDO:0011772", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011772", "name": "CDG-IId", 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Chem.", "date": "1995", "authors": "Yamaguchi N, Fukuda M N", "reference": { "type": "PubMed", "id": "7744867", "url": "https://pubmed.ncbi.nlm.nih.gov/7744867" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P15291-1", "protein_name": "Beta-1,4-galactosyltransferase 1", "gene_name": "B4GALT1", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P15291", "url": "https://www.uniprot.org/uniprotkb/P15291" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.7744867", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": "referenced_glycans", "table_stats": 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Commun.", "date": "1995", "authors": "Braun A, Kammerer S, B\u00f6hme E, M\u00fcller B, Roscher A A", "reference": { "type": "PubMed", "id": "7779090", "url": "https://pubmed.ncbi.nlm.nih.gov/7779090" }, "referenced_glycans": [], "referenced_proteins": [ { "uniprot_canonical_ac": "P30411-1", "protein_name": "B2 bradykinin receptor", "gene_name": "BDKRB2", "tax_name": "Human" } ], "species": [ { "name": "Homo sapiens", "taxid": 9606, "evidence": [ { "database": "UniProtKB", "id": "P30411", "url": "https://www.uniprot.org/uniprotkb/P30411" } ], "common_name": "Human", "glygen_name": "Human", "reference_species": "Homo sapiens [9606]" } ], "record_id": "pubmed.7779090", "abstract": "", "glycosylation": [], "mutagenesis": [], "snv": [], "phosphorylation": [], "glycation": [], "section_stats": [ { "table_id": "referenced_proteins", "table_stats": [ { "field": "total", "count": 1 } ], "sort_fields": [ "uniprot_canonical_ac", "protein_name", "gene_name", "tax_name" ] }, { "table_id": 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"Human C1q Tumor Necrosis Factor 8 (CTRP8) defines a novel tryptase+ mast cell subpopulation in the prostate cancer microenvironment.", "journal": "Biochimica et biophysica acta. 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