{
    "uniprot_canonical_ac": "A0A0R4IR84-1",
    "uniprot_id": [
        {
            "id": "A0A0R4IR84_DANRE",
            "url": "https://www.uniprot.org/uniprot/A0A0R4IR84_DANRE",
            "type": "external"
        }
    ],
    "mass": 101606.0,
    "length": 886,
    "protein_name": "Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1",
    "gene_name": "ndst1b",
    "organism": "Zebrafish",
    "refseq_name": "bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1b",
    "refseq_ac": [
        {
            "id": "NP_001311384",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001311384",
            "type": "external"
        }
    ],
    "gene_names_uniprotkb": "ndst1b; fj47c03; ndst1; wu:fj47c03",
    "gene_names_refseq": "fj47c03; ndst1; wu:fj47c03; ndst1b",
    "protein_names_uniprotkb": "Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1; 2.8.2.8; Glucosaminyl N-deacetylase/N-sulfotransferase 1",
    "protein_names_refseq": "N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1; bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1b",
    "tax_id": 7955,
    "disease": "autism spectrum disorder (Disease Ontology:DOID:0060041); autosomal recessive intellectual developmental disorder 46 (Disease Ontology:DOID:0081210); intellectual disability (Disease Ontology:DOID:1059); DiGeorge syndrome (Disease Ontology:DOID:11198); newborn respiratory distress syndrome (Disease Ontology:DOID:12716); azoospermia (Disease Ontology:DOID:14227); germ cell cancer (Disease Ontology:DOID:2994); congenital diaphragmatic hernia (Disease Ontology:DOID:3827)",
    "pathway": " (dre:570459);  (R-DRE-2022928)",
    "pathway_count": 2,
    "publication_count": 8,
    "publication_id_list": "19858418;23594743;24643020;25767878;27189481;31269894;33068391;36503154",
    "function": "##Evidence-Data-START## Transcript exon combination :: GFIL01024377.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA3505380, SAMEA3505383 [ECO:0000348] ##Evidence-Data-END## VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from BX072577.14 and LO018008.1. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments., [RefSeq]",
    "predicted_glycosites": 0,
    "predicted_n_glycosites": 0,
    "predicted_o_glycosites": 0,
    "mined_glycosites": 0,
    "mined_n_glycosites": 0,
    "mined_o_glycosites": 0,
    "reported_n_glycosites": 0,
    "reported_o_glycosites": 0,
    "reported_n_glycosites_with_glycan": 0,
    "reported_o_glycosites_with_glycan": 0,
    "total_reported_n_glycosites": 0,
    "total_reported_o_glycosites": 0,
    "total_n_glycosites": 0,
    "total_o_glycosites": 0,
    "reported_fully_resolved_glycans": 0,
    "reported_phosphosites": 0,
    "reported_mutagensis": 0,
    "reported_glycation": 0,
    "reported_snv": 0,
    "reported_interactions": 0,
    "missing_score": 10000,
    "biomarker_type": "",
    "glycan_count": 0,
    "disease_count": 8,
    "glyco_site_count": 0,
    "binding_glycan_count": 0,
    "secondary_ac_list": "",
    "ec_number_list": [
        {
            "id": "2.8.2.8",
            "url": "https://www.rhea-db.org/rhea/?query=ec:2.8.2.8",
            "type": "external"
        }
    ],
    "go_molecular_function": "GO:0016787 hydrolase activity;GO:0019213 deacetylase activity;GO:0015016 heparan sulfate N-sulfotransferase activity",
    "go_cellular_component": "GO:0005794 Golgi apparatus;GO:0016020 membrane",
    "go_biological_process": "GO:0051923 sulfation;GO:0001570 vasculogenesis;GO:0030210 heparin biosynthetic process;GO:0015014 heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process",
    "synthesized_glycan_count": 0,
    "record_id": "A0A0R4IR84-1",
    "record_type": "protein",
    "filter_code": "0000000.0000111.010000.0000000000000001.00000.000"
}