{
    "uniprot_canonical_ac": "A0A0R4ICC1-1",
    "uniprot_id": [
        {
            "id": "A0A0R4ICC1_DANRE",
            "url": "https://www.uniprot.org/uniprot/A0A0R4ICC1_DANRE",
            "type": "external"
        }
    ],
    "mass": 82033.0,
    "length": 728,
    "protein_name": "3.6.4.12; Twinkle mtDNA helicase; Twinkle protein, mitochondrial",
    "gene_name": "twnk",
    "organism": "Zebrafish",
    "refseq_name": "twinkle mtDNA helicase",
    "refseq_ac": [
        {
            "id": "NP_001264527",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001264527",
            "type": "external"
        }
    ],
    "gene_names_uniprotkb": "twnk; fi04d09; peo1; wu:fi04d09",
    "gene_names_refseq": "fi04d09; peo1; wu:fi04d09; twnk",
    "protein_names_uniprotkb": "3.6.4.12; Twinkle mtDNA helicase; Twinkle protein, mitochondrial",
    "protein_names_refseq": "twinkle mtDNA helicase; twinkle protein, mitochondrial-like; progressive external ophthalmoplegia 1",
    "tax_id": 7955,
    "disease": "Perrault syndrome (Disease Ontology:DOID:0050857); mitochondrial DNA depletion syndrome 7 (Disease Ontology:DOID:0080126); autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 (Disease Ontology:DOID:0111518); autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 (Disease Ontology:DOID:0111520); chronic progressive external ophthalmoplegia (Disease Ontology:DOID:12558); Parkinson's disease (Disease Ontology:DOID:14330)",
    "pathway": " (dre:100330448)",
    "pathway_count": 1,
    "publication_count": 9,
    "publication_id_list": "18335061;22465854;23516612;23594743;25771346;27189481;27924917;28535465;32806454",
    "function": "##Evidence-Data-START## Transcript exon combination        :: GDQH01006689.1 [ECO:0000332] RNAseq introns :: mixed sample support SAMEA3505370, SAMEA3505371 [ECO:0006172] ##Evidence-Data-END## ##RefSeq-Attributes-START## gene product(s) localized to mito. :: inferred from homology ##RefSeq-Attributes-END## VALIDATED REFSEQ: This record has undergone validation or preliminary review. The reference sequence was derived from FQ312018.3 and EV561328.1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript 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": 6,
    "glyco_site_count": 0,
    "binding_glycan_count": 0,
    "secondary_ac_list": "",
    "ec_number_list": [],
    "go_molecular_function": "GO:0005524 ATP binding;GO:0003697 single-stranded DNA binding;GO:0003678 DNA helicase activity;GO:0043139 5'-3' DNA helicase activity",
    "go_cellular_component": "GO:0005739 mitochondrion",
    "go_biological_process": "GO:0006264 mitochondrial DNA replication",
    "synthesized_glycan_count": 0,
    "record_id": "A0A0R4ICC1-1",
    "record_type": "protein",
    "filter_code": "0000000.0000111.100000.0000000000000001.00000.000"
}