{
    "uniprot_canonical_ac": "A0A0B4LGD3-1",
    "uniprot_ac": "A0A0B4LGD3",
    "uniprot_id": "A0A0B4LGD3_DROME",
    "mass": {
        "chemical_mass": 119705.0,
        "monoisotopic_mass": 119705.0
    },
    "refseq": {
        "ac": "NP_001286793",
        "name": "kazachoc, isoform E",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286793"
    },
    "gene_names": [
        {
            "name": "kcc",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "2R8; BEST:CK01510; CG2768; CG5594; CK01510; Dmel\\CG5594; DmKCC; E(sda)J; Kcc; KCC; l(2)60A-C; Line J; mdcds_17605",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726378",
            "id": "NP_726378"
        },
        {
            "name": "BEST:CK01510",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "CG2768",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "CG5594",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "CK01510",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "DmKCC",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "Dmel\\CG5594",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "Dmel_CG5594",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "E(sda)J",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "KCC",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "Kcc",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "Line J",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "kcc",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726378",
            "id": "NP_726378"
        },
        {
            "name": "l(2)60A-C",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "mdcds_17605",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "id": "A0A0B4LGD3"
        }
    ],
    "protein_names": [
        {
            "name": "CG5594-PA; kcc-PA; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726378",
            "id": "NP_726378"
        },
        {
            "name": "CG5594-PB; kcc-PB; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726379",
            "id": "NP_726379"
        },
        {
            "name": "CG5594-PC; kcc-PC; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_571976",
            "id": "NP_571976"
        },
        {
            "name": "CG5594-PE; kcc-PE; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286793",
            "id": "NP_001286793"
        },
        {
            "name": "CG5594-PF; kcc-PF; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286794",
            "id": "NP_001286794"
        },
        {
            "name": "CG5594-PG; kcc-PG; E(sda)J; lethal (2) 60A-C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286795",
            "id": "NP_001286795"
        },
        {
            "name": "Kazachoc, isoform G",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "A0A0B4LGD3"
        },
        {
            "name": "kazachoc, isoform A",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726378",
            "id": "NP_726378"
        },
        {
            "name": "kazachoc, isoform B",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_726379",
            "id": "NP_726379"
        },
        {
            "name": "kazachoc, isoform C",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_571976",
            "id": "NP_571976"
        },
        {
            "name": "kazachoc, isoform E",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286793",
            "id": "NP_001286793"
        },
        {
            "name": "kazachoc, isoform F",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286794",
            "id": "NP_001286794"
        },
        {
            "name": "kazachoc, isoform G",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286795",
            "id": "NP_001286795"
        }
    ],
    "function": [],
    "disease": [
        {
            "disease_id": "DOID:0080460",
            "recommended_name": {
                "id": "DOID:0080460",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080460",
                "name": "developmental and epileptic encephalopathy 34",
                "description": "A developmental and epileptic encephalopathy characterized by infantile onset of refractory migrating focal seizures, developmental regression and severe global impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SLC12A5 gene on chromosome 20q12."
            },
            "synonyms": [
                {
                    "id": "DOID:0080460",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080460",
                    "name": "early infantile epileptic encephalopathy 34",
                    "description": ""
                },
                {
                    "id": "DOID:0080460",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080460",
                    "name": "DEE34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "developmental and epileptic encephalopathy, 34",
                    "description": "Any early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the SLC12A5 gene."
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "DEE34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "EIEE34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "SLC12A5 early infantile epileptic encephalopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "developmental and epileptic encephalopathy 34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "early infantile epileptic encephalopathy caused by mutation in SLC12A5",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "epileptic encephalopathy, early infantile, 34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "epileptic encephalopathy, early infantile, 34; EIEE34",
                    "description": ""
                },
                {
                    "id": "MONDO:0014718",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014718",
                    "name": "epileptic encephalopathy, early infantile, type 34",
                    "description": ""
                },
                {
                    "id": "MIM:616645",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/616645",
                    "name": "Developmental and epileptic encephalopathy 34",
                    "description": "Developmental and epileptic encephalopathy 34"
                }
            ],
            "evidence": [
                {
                    "id": "0080460",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080460"
                }
            ]
        },
        {
            "disease_id": "DOID:0090003",
            "recommended_name": {
                "id": "DOID:0090003",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0090003",
                "name": "agenesis of the corpus callosum with peripheral neuropathy",
                "description": "A neurodegenerative disease characterized by autosomal recessive inheritance with early onset of severe sensory-motor polyneuropathy, variable degree of agenesis of the corpus callosum, amyotrophy, hypotonia, and cognitive impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SLC12A6 gene on chromosome 15q14."
            },
            "synonyms": [
                {
                    "id": "DOID:0090003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0090003",
                    "name": "Andermann syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:0090003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0090003",
                    "name": "Charlevoix disease",
                    "description": ""
                },
                {
                    "id": "DOID:0090003",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0090003",
                    "name": "corpus callosum agenesis-neuronopathy syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "agenesis of the corpus callosum with peripheral neuropathy",
                    "description": "Corpus callosum agenesis-neuropathy is a neurodegenerative disorder characterized by severe progressive sensorimotor neuropathy beginning in infancy with resulting hypotonia, areflexia, amyotrophy and variable degrees of dysgenesis of the corpus callosum. Additional features include mild-to-severe intellectual and developmental delays, and psychiatric manifestations that include paranoid delusions, depression, hallucinations, and 'autistic-like' features. Affected individuals are usually wheelchair restricted in the second decade of life and die in the third decade of life. The disease is inherited as an autosomal recessive trait."
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "Andermann syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "Charlevoix disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "agenesis of the corpus callosum with peripheral neuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "corpus callosum agenesis-neuronopathy syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "hereditary motor and sensory neuropathy with agenesis of the corpus callosum",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "peripheral neuropathy associated with agenesis of the corpus callosum",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "ACCPN",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "HMSN/ACC",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "agenesis of corpus callosum with neuronopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "agenesis of corpus callosum with peripheral neuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "agenesis of corpus callosum with polyneuropathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "corpus callosum agenesis neuronopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "corpus callosum, agenesis of, with neuronopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0000902",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0000902",
                    "name": "polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum",
                    "description": ""
                },
                {
                    "id": "MIM:218000",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/218000",
                    "name": "Agenesis of the corpus callosum, with peripheral neuropathy",
                    "description": "Agenesis of the corpus callosum, with peripheral neuropathy"
                }
            ],
            "evidence": [
                {
                    "id": "0090003",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0090003"
                }
            ]
        },
        {
            "disease_id": "DOID:0111315",
            "recommended_name": {
                "id": "DOID:0111315",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111315",
                "name": "idiopathic generalized epilepsy 14",
                "description": "An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the SLC12A5 on chromosome 20q13.12."
            },
            "synonyms": [
                {
                    "id": "DOID:0111315",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111315",
                    "name": "EIG14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "epilepsy, idiopathic generalized, susceptibility to, 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "EIG14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "epilepsy, idiopathic generalized, susceptibility to, 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "epilepsy, idiopathic generalized, susceptibility to, 14; EIG14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "epilepsy, idiopathic generalized, susceptibility to, type 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "susceptibility to idiopathic generalised epilepsy 14",
                    "description": ""
                },
                {
                    "id": "MONDO:0014734",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0014734",
                    "name": "susceptibility to idiopathic generalized epilepsy 14",
                    "description": ""
                },
                {
                    "id": "MIM:616685",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/616685",
                    "name": "Epilepsy, idiopathic generalized 14",
                    "description": "Epilepsy, idiopathic generalized 14"
                }
            ],
            "evidence": [
                {
                    "id": "0111315",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111315"
                }
            ]
        },
        {
            "disease_id": "DOID:10595",
            "recommended_name": {
                "id": "DOID:10595",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:10595",
                "name": "Charcot-Marie-Tooth disease",
                "description": "A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm."
            },
            "synonyms": [
                {
                    "id": "DOID:10595",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:10595",
                    "name": "CMT - Charcot-Marie-Tooth disease",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth disease type 1A",
                    "description": "Charcot-Marie-Tooth disease type 1A (CMT1A) is a type ofinherited neurological disorder that affects the peripheral nerves. Affected individuals experience weakness and wasting (atrophy) of the muscles of the lower legs beginning in adolescence; later they experience hand weakness and sensory loss. CMT1A is caused byhaving an extra copy (a duplication) of the PMP22 gene. It is inherited in an autosomal dominant manner. Treatment for this condition may include physical therapy ; occupational therapy ; braces and other orthopedic devices; orthopedic surgery;and pain medications."
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "CMT1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth disease type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth disease, type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth neuropathy type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth syndrome type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "HMSN1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "hereditary motor and sensory neuropathy 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "microduplication 17p12",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "CMT 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot Marie Tooth disease type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth disease, demyelinating, type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "Charcot-Marie-Tooth neuropathy, type 1A",
                    "description": ""
                },
                {
                    "id": "MONDO:0007309",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0007309",
                    "name": "HMSN 1A",
                    "description": ""
                },
                {
                    "id": "MIM:118220",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/118220",
                    "name": "Charcot-Marie-Tooth disease, demyelinating, 1A",
                    "description": "Charcot-Marie-Tooth disease, demyelinating, 1A"
                }
            ],
            "evidence": [
                {
                    "id": "10595",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:10595"
                }
            ]
        },
        {
            "disease_id": "DOID:1826",
            "recommended_name": {
                "id": "DOID:1826",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1826",
                "name": "epilepsy",
                "description": "A brain disease that is characterized by the occurrance of at least two unprovoked seizures resulting from a persistent epileptogenic abnormality of the brain that is able to spontaneously generate paroxysmal activity and typically manifested by sudden brief episodes of altered or diminished consciousness, involuntary movements, or convulsions."
            },
            "synonyms": [
                {
                    "id": "DOID:1826",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1826",
                    "name": "epilepsy syndrome",
                    "description": ""
                },
                {
                    "id": "DOID:1826",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1826",
                    "name": "epileptic syndrome",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1826",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1826"
                }
            ]
        },
        {
            "disease_id": "DOID:2477",
            "recommended_name": {
                "id": "DOID:2477",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2477",
                "name": "motor peripheral neuropathy",
                "description": "A neuropathy that is characterized by inflammation or degeneration of the peripheral motor nerves."
            },
            "synonyms": [
                {
                    "id": "DOID:2477",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2477",
                    "name": "HSMN",
                    "description": ""
                },
                {
                    "id": "DOID:2477",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2477",
                    "name": "HSMN - Hereditary sensory and motor neuropathy",
                    "description": ""
                },
                {
                    "id": "DOID:2477",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2477",
                    "name": "Hereditary motor and sensory neuropathy",
                    "description": ""
                },
                {
                    "id": "DOID:2477",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2477",
                    "name": "neuropathic muscular atrophy",
                    "description": ""
                },
                {
                    "id": "DOID:2477",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2477",
                    "name": "Peripheral Motor Neuropathy",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "2477",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:2477"
                }
            ]
        }
    ],
    "snv": [],
    "mutagenesis": [],
    "expression_tissue": [],
    "expression_disease": [],
    "species": [
        {
            "name": "Drosophila melanogaster",
            "taxid": 7227,
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "A0A0B4LGD3",
                    "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                }
            ],
            "common_name": "Fruit fly"
        }
    ],
    "gene": [
        {
            "name": "kcc",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
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                "start_pos": 23925066,
                "end_pos": 23907654,
                "strand": "-",
                "evidence": [
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                        "database": "Ensembl Gene",
                        "id": "FBgn0261794",
                        "url": "https://www.ensembl.org/id/FBgn0261794"
                    }
                ]
            }
        }
    ],
    "crossref": [
        {
            "id": "FBgn0261794",
            "url": "https://bgee.org/?page=gene&gene_id=FBgn0261794",
            "database": "Bgee",
            "categories": [
                "Gene Expression"
            ]
        },
        {
            "id": "FBgn0261794",
            "url": "https://flybase.org/reports/FBgn0261794",
            "database": "FlyBase",
            "categories": [
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            ]
        },
        {
            "id": "37800",
            "url": "https://www.ncbi.nlm.nih.gov/gene/37800",
            "database": "GeneID",
            "categories": [
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            ]
        },
        {
            "id": "Q9W1G6",
            "url": "https://www.ebi.ac.uk/intact/interactors/id:Q9W1G6*",
            "database": "IntAct",
            "categories": [
                "Other"
            ]
        },
        {
            "id": "IPR000076",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000076",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR004841",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR004841",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR004842",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR004842",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "IPR018491",
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR018491",
            "database": "InterPro",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "dme:Dmel_CG5594",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG5594",
            "database": "KEGG Pathway",
            "categories": [
                "Enzyme and Pathway"
            ]
        },
        {
            "id": "KNWRPHI",
            "url": "https://omabrowser.org/oma/group/KNWRPHI/",
            "database": "OMA",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "5490251at2759",
            "url": "http://www.orthodb.org/?query=5490251at2759",
            "database": "OrthoDB",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11827",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11827",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PTHR11827:SF73",
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR11827:SF73",
            "database": "PANTHER",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF00324",
            "url": "http://pfam.xfam.org/family/PF00324",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "PF03522",
            "url": "http://pfam.xfam.org/family/PF03522",
            "database": "Pfam",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "R-DME-426117",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-426117",
            "database": "Reactome",
            "categories": [
                "Protein Classification"
            ]
        },
        {
            "id": "NP_001286795",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001286795",
            "database": "RefSeq",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "72427",
            "url": "https://www.rhea-db.org/rhea/72427",
            "database": "Rhea",
            "categories": [
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            ]
        },
        {
            "id": "A0A0B4LGD3",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LGD3-1",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LHE0",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LHE0",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "A0A0B4LHE0-1",
            "url": "https://www.uniprot.org/uniprot/A0A0B4LHE0-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MKK5",
            "url": "https://www.uniprot.org/uniprot/Q8MKK5",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MKK5-1",
            "url": "https://www.uniprot.org/uniprot/Q8MKK5-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MLQ5",
            "url": "https://www.uniprot.org/uniprot/Q8MLQ5",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q8MLQ5-1",
            "url": "https://www.uniprot.org/uniprot/Q8MLQ5-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1G5",
            "url": "https://www.uniprot.org/uniprot/Q9W1G5",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1G5-1",
            "url": "https://www.uniprot.org/uniprot/Q9W1G5-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1G6",
            "url": "https://www.uniprot.org/uniprot/Q9W1G6",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        },
        {
            "id": "Q9W1G6-1",
            "url": "https://www.uniprot.org/uniprot/Q9W1G6-1",
            "database": "UniProtKB",
            "categories": [
                "Protein"
            ]
        }
    ],
    "sequence": {
        "sequence": "MQSNSAKDDSDEMEIIPSEHNGTVHETKNEDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVVQTIMDYKETPSDNKMSLVQTIVDHHYDATKTASKVRFADPTIEETQHHDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
        "length": 1077,
        "header": "tr|A0A0B4LGD3-1|A0A0B4LGD3_DROME Isoform 1 of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=1 CANONICAL=A0A0B4LGD3-1"
    },
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        {
            "isoform_ac": "A0A0B4LGD3-1",
            "url": "",
            "sequence": {
                "sequence": "MQSNSAKDDSDEMEIIPSEHNGTVHETKNEDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVVQTIMDYKETPSDNKMSLVQTIVDHHYDATKTASKVRFADPTIEETQHHDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1077,
                "header": "tr|A0A0B4LGD3-1|A0A0B4LGD3_DROME Isoform 1 of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=1 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23911461,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0343301",
                        "url": "https://www.ensembl.org/id/FBtr0343301"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0309966",
                        "url": "https://www.ensembl.org/id/FBpp0309966"
                    }
                ]
            }
        },
        {
            "isoform_ac": "A0A0B4LHE0-1",
            "url": "",
            "sequence": {
                "sequence": "MPDRFQVTKADEDTALDYNQDESASGKLLGDIHDETLDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVVQTIVDHHYDATKTASKVRFADPTIEETQHHDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1066,
                "header": "tr|A0A0B4LHE0-1|A0A0B4LHE0_DROME Computationally mapped isoform of Kazachoc, isoform F  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=1 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23909698,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0343300",
                        "url": "https://www.ensembl.org/id/FBtr0343300"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0309965",
                        "url": "https://www.ensembl.org/id/FBpp0309965"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q8MKK5-1",
            "url": "",
            "sequence": {
                "sequence": "MQSNSAKDDSDEMEIIPSEHNGTVHETKNEDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1028,
                "header": "tr|Q8MKK5-1|A0A0B4LGD3_DROME Computationally mapped isoform of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=1 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23911461,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0072138",
                        "url": "https://www.ensembl.org/id/FBtr0072138"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0072047",
                        "url": "https://www.ensembl.org/id/FBpp0072047"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q8MLQ5-1",
            "url": "",
            "sequence": {
                "sequence": "MPDRFQVTKADEDTALDYNQDESASGKLLGDIHDETLGENYGSYDDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVVQTIVDHHYDATKTASKVRFADPTIEETQHHDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1074,
                "header": "tr|Q8MLQ5-1|A0A0B4LGD3_DROME Computationally mapped isoform of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=1 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23909698,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0072137",
                        "url": "https://www.ensembl.org/id/FBtr0072137"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0072046",
                        "url": "https://www.ensembl.org/id/FBpp0072046"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9W1G5-1",
            "url": "",
            "sequence": {
                "sequence": "MQSNSAKDDSDEMEIIPSEHNGTVHETKNEDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVVQTIVDHHYDATKTASKVRFADPTIEETQHHDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1059,
                "header": "tr|Q9W1G5-1|A0A0B4LGD3_DROME Computationally mapped isoform of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=2 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23911461,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0072139",
                        "url": "https://www.ensembl.org/id/FBtr0072139"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0072048",
                        "url": "https://www.ensembl.org/id/FBpp0072048"
                    }
                ]
            }
        },
        {
            "isoform_ac": "Q9W1G6-1",
            "url": "",
            "sequence": {
                "sequence": "MPDRFQVTKADEDTALDYNQDESASGKLLGDIHDETLGENYGSYDDSGDIHRAEENQKSSIDPNLYLYDDDLETRPHISTFISSIANYENTIPAATDPDAKPAAPSARMGTLIGVFLPCIQNIFGVILFIRLTWVVGTAGAVCGFLIVLTCCCVTMLTAISMSAIATNGVVPAGGSYFMISRSLGPEFGGAVGMLFYTGTTLAAAMYIVGAVEIVLTYMAPWASIFGDFTKDADAMYNNFRVYGTLLLIFMGLIVFLGVKFVNKFATVALACVILSIIAVYVGIFDNIHGNEKLYMCVLGKRLLKDIPLENCTKEDSFLRDIYCPDGKCEEYYLANNVTKVKGIKGLASGVFYDNIFPSFLEKGQFISYGKSAIDIENTSGESYNQIMADITTSFTLLIGIFFPSVTGIMAGSNRSGDLADAQKSIPIGTICAILTTSTVYLSSVMFFAGTVDNLLLRDKFGQSIGGKLVVANIAWPNQWVILIGSFLSTLGAGLQSLTGAPRLLQAIARDEIIPFLAPFAKSSKRGEPTRALLLTIVICQCGILLGNVDLLAPLLSMFFLMCYGFVNLACAVQTLLRTPNWRPRFKFYHWSLSLIGLTLCISVMIMTSWYFALIAMGMAIIIYKYIEYRGAEKEWGDGIRGMALTAARYSLLRLEEGPPHTKNWRPQILVLSKLNDNLLPKYRKIFSFATQLKAGKGLTICVSVIKGDHTKITNKAVDAKATLRKYMTDEKVKGFCDVLVAQQIGEGLSSVIQTIGLGGMKPNTVIIGWPYSWRQEGRNSWKTFIQTVRTVAACHMALMVPKGINFYPESNHKIGGNIDIWWIVHDGGLLMLLPFLLKQHRTWRNCKLRIFTVAQIEDNSIQMKKDLKTFLYHLRIEADVEVVEMNNSDISAYTYERTLMMEQRNQMLRALGLNKKENSKVDSQNDEKRNSIDLDGPENADTPETTSNKDESTEKADGDFKSSVKPDEFNVRRMHTAIKLNEVIVEKSQDAQLVIMNLPGPPREVRAERERNYMEFLEVLTEGLEKVLMVRGGGREVITIYS",
                "length": 1043,
                "header": "tr|Q9W1G6-1|A0A0B4LGD3_DROME Computationally mapped isoform of Kazachoc, isoform G  OS=Drosophila melanogaster OX=7227 GN=kcc PE=1 SV=2 CANONICAL=A0A0B4LGD3-1"
            },
            "locus": {
                "chromosome": "2R",
                "start_pos": 23924906,
                "end_pos": 23909698,
                "strand": "-",
                "evidence": [
                    {
                        "database": "Ensembl Transcript",
                        "id": "FBtr0072136",
                        "url": "https://www.ensembl.org/id/FBtr0072136"
                    },
                    {
                        "database": "Ensembl Peptide",
                        "id": "FBpp0072045",
                        "url": "https://www.ensembl.org/id/FBpp0072045"
                    }
                ]
            }
        }
    ],
    "glycosylation": [],
    "phosphorylation": [],
    "glycation": [],
    "keywords": [],
    "publication": [],
    "pathway": [
        {
            "id": "dme:Dmel_CG5594",
            "name": "",
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+dme:Dmel_CG5594",
            "resource": "KEGG Pathway"
        },
        {
            "id": "R-DME-426117",
            "name": "Cation-coupled Chloride cotransporters",
            "url": "https://www.reactome.org/PathwayBrowser/#R-DME-426117",
            "resource": "Reactome",
            "description": "Cation-coupled Chloride cotransporters"
        }
    ],
    "orthologs": [],
    "go_annotation": {
        "categories": [
            {
                "name": "Biological Process",
                "total": 9,
                "go_terms": [
                    {
                        "name": "mechanosensory behavior",
                        "id": "GO:0007638",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007638",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "chemical synaptic transmission",
                        "id": "GO:0007268",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007268",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "cell volume homeostasis",
                        "id": "GO:0006884",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006884",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "response to mechanical stimulus",
                        "id": "GO:0009612",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009612",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "chloride transmembrane transport",
                        "id": "GO:1902476",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1902476",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "potassium ion homeostasis",
                        "id": "GO:0055075",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055075",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "potassium ion import across plasma membrane",
                        "id": "GO:1990573",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1990573",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "chloride ion homeostasis",
                        "id": "GO:0055064",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0055064",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "amino acid transmembrane transport",
                        "id": "GO:0003333",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003333",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Cellular Component",
                "total": 4,
                "go_terms": [
                    {
                        "name": "plasma membrane",
                        "id": "GO:0005886",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "axon",
                        "id": "GO:0030424",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "neuronal cell body",
                        "id": "GO:0043025",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043025",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "synapse",
                        "id": "GO:0045202",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045202",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            },
            {
                "name": "Molecular Function",
                "total": 2,
                "go_terms": [
                    {
                        "name": "amino acid transmembrane transporter activity",
                        "id": "GO:0015171",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015171",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    },
                    {
                        "name": "potassium:chloride symporter activity",
                        "id": "GO:0015379",
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0015379",
                        "evidence": [
                            {
                                "database": "UniProtKB",
                                "id": "A0A0B4LGD3",
                                "url": "https://www.uniprot.org/uniprot/A0A0B4LGD3"
                            }
                        ],
                        "pmid": ""
                    }
                ]
            }
        ]
    },
    "pro_annotation": [],
    "site_annotation": [
        {
            "start_pos": 21,
            "end_pos": 23,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 296,
            "end_pos": 298,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 322,
            "end_pos": 324,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 363,
            "end_pos": 365,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 399,
            "end_pos": 401,
            "annotation": "n_glycosylation_sequon"
        },
        {
            "start_pos": 872,
            "end_pos": 874,
            "annotation": "n_glycosylation_sequon"
        }
    ],
    "ptm_annotation": [],
    "interactions": [],
    "reactions": [
        {
            "id": "72427",
            "name": "",
            "equation": "chloride(in) + K(+)(in) = chloride(out) + K(+)(out)",
            "summary": "",
            "cellular_location": "",
            "input_participant_list": [],
            "output_participant_list": [],
            "enzyme_list": [],
            "evidence": [
                {
                    "id": "72427",
                    "database": "Rhea",
                    "url": "https://www.rhea-db.org/rhea/72427"
                }
            ]
        }
    ],
    "reaction_participants": [],
    "reaction_enzymes": [],
    "biomarkers": [],
    "synthesized_glycans": [],
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb",
            "label": "Isoforms"
        }
    ],
    "section_stats": [
        {
            "table_id": "glycosylation",
            "table_stats": [
                {
                    "field": "total",
                    "count": 0
                },
                {
                    "field": "total_sites",
                    "count": 0
                },
                {
                    "field": "n_linked_glycans",
                    "count": 0
                },
                {
                    "field": "n_linked_glycan_sites",
                    "count": 0
                },
                {
                    "field": "o_linked_glycans",
                    "count": 0
                },
                {
                    "field": "o_linked_glycan_sites",
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                }
            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported",
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                    "field": "total",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "glycosylation_reported_with_glycan",
            "table_stats": [
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                    "field": "total",
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                {
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                    "field": "total",
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            "sort_fields": []
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        {
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                {
                    "field": "o_linked_glycan_sites",
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            ],
            "sort_fields": []
        },
        {
            "table_id": "phosphorylation",
            "table_stats": [
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                    "field": "total",
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                {
                    "field": "total_sites",
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            ],
            "sort_fields": []
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        {
            "table_id": "snv",
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            ],
            "sort_fields": []
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        {
            "table_id": "snv_disease",
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        {
            "table_id": "snv_non_disease",
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                    "field": "total",
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            "sort_fields": []
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        {
            "table_id": "publication",
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                    "count": 0
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            "sort_fields": []
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    ]
}