{ "uniprot_canonical_ac": "Q8IP51-1", "uniprot_ac": "Q8IP51", "uniprot_id": "Q8IP51_DROME", "mass": { "chemical_mass": 374749.0, "monoisotopic_mass": 374749.0 }, "refseq": { "ac": "NP_723870", "name": "wing blister, isoform B", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870" }, "gene_names": [ { "name": "wb", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "2; 2Lan; 2]]; A1; alpha1; alpha[[1; BEST:CK02229; BG:DS03792.1; BG:DS03792.2; CG15288; CG32970; CG42677; CK02229; CT35236; DLAM; Dmel\\CG42677; fus5; l(2)09437; l(2)34Fb; l(2)br1; l34Fb; LanA1; LanWb; LM-A/alpha2; Wb", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870", "id": "NP_723870" }, { "name": "2Lan", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "2]]", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "2", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "A1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "BEST:CK02229", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "BG:DS03792.1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "BG:DS03792.2", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "CG15288", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "CG32970", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "CG42677", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "CK02229", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "CT35236", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "DLAM", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "Dmel\\CG42677", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "Dmel_CG42677", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "LanA1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "LanWb", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "Wb", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "alpha1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "alpha2", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "alpha[[1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "fus5", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "l(2)09437", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "l(2)34Fb", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "l(2)br1", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "l34Fb", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprot/Q8IP51", "id": "Q8IP51" }, { "name": "wb", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870", "id": "NP_723870" } ], "protein_names": [ { "name": "CG42677-PB; wb-PB; lethal group A1; laminin A2; alpha laminin; wing blistered; D-laminin alpha2; SGP cluster fusion defects 5; lamininW; wingblister; lethal 1 in the black-reduced region; laminin alpha1,2; laminin alpha[[1,2]]", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870", "id": "NP_723870" }, { "name": "CG42677-PC; wb-PC; lethal group A1; laminin A2; alpha laminin; wing blistered; D-laminin alpha2; SGP cluster fusion defects 5; lamininW; wingblister; lethal 1 in the black-reduced region; laminin alpha1,2; laminin alpha[[1,2]]", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001188806", "id": "NP_001188806" }, { "name": "CG42677-PG; wb-PG; lethal group A1; laminin A2; alpha laminin; wing blistered; D-laminin alpha2; SGP cluster fusion defects 5; lamininW; wingblister; lethal 1 in the black-reduced region; laminin alpha1,2; laminin alpha[[1,2]]", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_476790", "id": "NP_476790" }, { "name": "Wing blister, isoform B", "resource": "UniProtKB", "type": "synonym", "url": "", "id": "Q8IP51" }, { "name": "wing blister, isoform B", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870", "id": "NP_723870" }, { "name": "wing blister, isoform C", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001188806", "id": "NP_001188806" }, { "name": "wing blister, isoform G", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_476790", "id": "NP_476790" } ], "function": [], "disease": [ { "disease_id": "DOID:0110274", "recommended_name": { "id": "DOID:0110274", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110274", "name": "autosomal recessive limb-girdle muscular dystrophy", "description": "A limb-girdle muscular dystrophy has_material_basis_in autosomal recessive inheritance." }, "synonyms": [ { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "autosomal recessive limb-girdle muscular dystrophy type 2A", "description": "Autosomal recessive limb-girdle muscular dystrophy type 2A (LGMD2A) is a subtype of autosomal recessive limb girdle muscular dystrophy characterized by a variable age of onset of progressive, typically symmetrical and selective weakness and atrophy of proximal shoulder- and pelvic-girdle muscles (gluteus maximus, thigh adductors, and muscles of the posterior compartment of the limbs are most commonly affected) without cardiac or facial involvement. Clinical manifestations include exercise intolerance, a waddling gait, scapular winging and calf pseudo-hypertrophy." }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "CAPN3 autosomal recessive limb-girdle muscular dystrophy", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "LGMD2A", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "Leyden-Moebius muscular dystrophy", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "autosomal recessive limb-girdle muscular dystrophy type 2A", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "calpainopathy", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "limb-girdle muscular dystrophy due to calpain deficiency", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "limb-girdle muscular dystrophy type 2A", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "muscular dystrophy, limb-girdle, autosomal recessive 1", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "muscular dystrophy, limb-girdle, type 2A", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "pelvofemoral muscular dystrophy", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "primary calpainopathy", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "LGMD2", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "limb-girdle muscular dystrophy type 2", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "muscular dystrophy limb girdle type 2A, erb type", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "muscular dystrophy, Pelvofemoral", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "muscular dystrophy, limb-girdle, type 2", "description": "" }, { "id": "MONDO:0009675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009675", "name": "myositis, eosinophilic", "description": "" }, { "id": "MIM:253600", "resource": "MIM", "url": "https://www.omim.org/entry/253600", "name": "Muscular dystrophy, limb-girdle, autosomal recessive 1", "description": "Muscular dystrophy, limb-girdle, autosomal recessive 1" } ], "evidence": [ { "id": "0110274", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0110274" } ] }, { "disease_id": "DOID:0110636", "recommended_name": { "id": "DOID:0110636", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110636", "name": "congenital merosin-deficient muscular dystrophy 1A", "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscle weakness that is apparent at birth or in the first 6 months of life and frequent development of periventricular white matter abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22." }, "synonyms": [ { "id": "DOID:0110636", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110636", "name": "CMD1A", "description": "" }, { "id": "DOID:0110636", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110636", "name": "MDC1A", "description": "" }, { "id": "DOID:0110636", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110636", "name": "Merosin-negative congenital muscular dystrophy", "description": "" }, { "id": "DOID:0110636", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110636", "name": "congenital muscular dystrophy due to laminin alpha2 deficiency", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "congenital merosin-deficient muscular dystrophy 1A", "description": "Congenital muscular dystrophy type 1A (MCD1A) belongs to a group of neuromuscular disorders with onset at birth or infancy characterized by hypotonia, muscle weakness and muscle wasting." }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "CMD1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "LAMA2 congenital muscular dystrophy", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "MDC1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "congenital merosin-deficient muscular dystrophy type 1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "congenital muscular dystrophy caused by mutation in LAMA2", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "congenital muscular dystrophy due to laminin alpha2 deficiency", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "merosin-deficient congenital muscular dystrophy type 1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "merosin-negative congenital muscular dystrophy", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital merosin-deficient, type 1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital, merosin deficient or partially deficient", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "LAMA2-related muscular dystrophy", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "congenital muscular dystrophy type 1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "laminin alpha-2 deficiency", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "merosin-deficient congenital muscular dystrophy", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital merosin-deficient", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital merosin-deficient, 1A", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital, due to partial LAMA2 deficiency", "description": "" }, { "id": "MONDO:0011925", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011925", "name": "muscular dystrophy, congenital, merosin-deficient", "description": "" }, { "id": "MIM:607855", "resource": "MIM", "url": "https://www.omim.org/entry/607855", "name": "Merosin-deficient congenital muscular dystrophy 1A", "description": "Merosin-deficient congenital muscular dystrophy 1A" } ], "evidence": [ { "id": "0110636", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0110636" } ] }, { "disease_id": "DOID:11830", "recommended_name": { "id": "DOID:11830", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:11830", "name": "myopia", "description": "A refractive error characterized by the inability to see farther objects clearly." }, "synonyms": [ { "id": "DOID:11830", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:11830", "name": "near vision", "description": "" }, { "id": "DOID:11830", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:11830", "name": "near-sightedness", "description": "" }, { "id": "DOID:11830", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:11830", "name": "short-sightedness", "description": "" }, { "id": "MONDO:0012229", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012229", "name": "myopia 9", "description": "" }, { "id": "MONDO:0012229", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012229", "name": "MYP9", "description": "" }, { "id": "MONDO:0012229", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012229", "name": "myopia 9", "description": "" }, { "id": "MONDO:0012230", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012230", "name": "myopia 10", "description": "" }, { "id": "MONDO:0012230", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012230", "name": "MYP10", "description": "" }, { "id": "MONDO:0012230", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012230", "name": "myopia 10", "description": "" }, { "id": "MONDO:0012227", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012227", "name": "myopia 7", "description": "" }, { "id": "MONDO:0012227", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012227", "name": "MYP7", "description": "" }, { "id": "MONDO:0012227", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012227", "name": "myopia 7", "description": "" }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "schizophrenia 16", "description": "A schizophrenia that has material basis in a mutation on chromosome 7q36.3." }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "SCZD16", "description": "" }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "schizophrenia 16", "description": "" }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "schizophrenia type 16", "description": "" }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "chromosome 7Q36.3 Duplication syndrome, 362-Kb", "description": "" }, { "id": "MONDO:0013506", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013506", "name": "schizophrenia susceptibility locus, chromosome 7Q36.3-related", "description": "" }, { "id": "MONDO:0010685", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010685", "name": "myopia 1, X-linked", "description": "" }, { "id": "MONDO:0010685", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010685", "name": "MYP1", "description": "" }, { "id": "MONDO:0010685", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010685", "name": "myopia 1, X-linked", "description": "" }, { "id": "MONDO:0010685", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010685", "name": "myopia-1, X-linked recessive", "description": "" }, { "id": "MONDO:0012995", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012995", "name": "myopia 15, autosomal dominant", "description": "" }, { "id": "MONDO:0012995", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012995", "name": "MYP15", "description": "" }, { "id": "MONDO:0012995", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012995", "name": "myopia 15, autosomal dominant", "description": "" }, { "id": "MONDO:0013604", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013604", "name": "myopia 21, autosomal dominant", "description": "Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene." }, { "id": "MONDO:0013604", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013604", "name": "ZNF644 myopia (disease)", "description": "" }, { "id": "MONDO:0013604", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013604", "name": "myopia (disease) caused by mutation in ZNF644", "description": "" }, { "id": "MONDO:0013604", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013604", "name": "myopia 21, autosomal dominant", "description": "" }, { "id": "MONDO:0013604", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013604", "name": "MYP21", "description": "" }, { "id": "MONDO:0014177", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014177", "name": "myopia 22, autosomal dominant", "description": "" }, { "id": "MONDO:0014177", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014177", "name": "myopia 22, autosomal dominant", "description": "" }, { "id": "MONDO:0014177", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014177", "name": "MYP22", "description": "" }, { "id": "MONDO:0009713", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009713", "name": "myopia 18, autosomal recessive", "description": "" }, { "id": "MONDO:0009713", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009713", "name": "MYP18", "description": "" }, { "id": "MONDO:0009713", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0009713", "name": "myopia 18, autosomal recessive", "description": "" }, { "id": "MONDO:0014411", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014411", "name": "myopia 24, autosomal dominant", "description": "" }, { "id": "MONDO:0014411", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014411", "name": "myopia 24, autosomal dominant", "description": "" }, { "id": "MONDO:0014411", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014411", "name": "MYP24", "description": "" }, { "id": "MONDO:0012228", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012228", "name": "myopia 8", "description": "" }, { "id": "MONDO:0012228", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012228", "name": "MYP8", "description": "" }, { "id": "MONDO:0012228", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012228", "name": "myopia 8", "description": "" }, { "id": "MONDO:0014183", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014183", "name": "myopia 23, autosomal recessive", "description": "" }, { "id": "MONDO:0014183", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014183", "name": "myopia 23, autosomal recessive", "description": "" }, { "id": "MONDO:0014183", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014183", "name": "MYP23", "description": "" }, { "id": "MONDO:0011300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011300", "name": "myopia 3, autosomal dominant", "description": "" }, { "id": "MONDO:0011300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011300", "name": "MYP3", "description": "" }, { "id": "MONDO:0011300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011300", "name": "myopia 3, autosomal dominant", "description": "" }, { "id": "MONDO:0011300", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011300", "name": "myopia-3", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "myopia 6", "description": "Any myopia in which the cause of the disease is a mutation in the SCO2 gene." }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "SCO2 myopia (disease)", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "myopia (disease) caused by mutation in SCO2", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "myopia 6", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "myopia type 6", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "MYP6", "description": "" }, { "id": "MONDO:0012154", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012154", "name": "myopia, susceptibility to", "description": "" }, { "id": "MONDO:0012389", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012389", "name": "myopia 12, autosomal dominant", "description": "" }, { "id": "MONDO:0012389", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012389", "name": "MYP12", "description": "" }, { "id": "MONDO:0012389", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012389", "name": "myopia 12", "description": "" }, { "id": "MONDO:0012389", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012389", "name": "myopia 12, autosomal dominant", "description": "" }, { "id": "MONDO:0012388", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012388", "name": "myopia 11, autosomal dominant", "description": "" }, { "id": "MONDO:0012388", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012388", "name": "MYP11", "description": "" }, { "id": "MONDO:0012388", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012388", "name": "myopia 11", "description": "" }, { "id": "MONDO:0012388", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012388", "name": "myopia 11, autosomal dominant", "description": "" }, { "id": "MONDO:0010377", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010377", "name": "myopia 13, X-linked", "description": "" }, { "id": "MONDO:0010377", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010377", "name": "MYP13", "description": "" }, { "id": "MONDO:0010377", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010377", "name": "myopia 13", "description": "" }, { "id": "MONDO:0010377", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010377", "name": "myopia 13, X-linked", "description": "" }, { "id": "MONDO:0012021", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012021", "name": "myopia 17, autosomal dominant", "description": "" }, { "id": "MONDO:0012021", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012021", "name": "MYP17", "description": "" }, { "id": "MONDO:0012021", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012021", "name": "myopia 17, autosomal dominant", "description": "" }, { "id": "MONDO:0012021", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012021", "name": "myopia 4", "description": "" }, { "id": "MONDO:0012021", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012021", "name": "myopia 4, formerly", "description": "" }, { "id": "MONDO:0012469", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012469", "name": "myopia 14", "description": "" }, { "id": "MONDO:0012469", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012469", "name": "MYP14", "description": "" }, { "id": "MONDO:0012469", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012469", "name": "myopia 14", "description": "" }, { "id": "MONDO:0012045", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012045", "name": "myopia 5, autosomal dominant", "description": "" }, { "id": "MONDO:0012045", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012045", "name": "MYP5", "description": "" }, { "id": "MONDO:0012045", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012045", "name": "myopia 5, autosomal dominant", "description": "" }, { "id": "MONDO:0008053", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008053", "name": "myopia 2, autosomal dominant", "description": "" }, { "id": "MONDO:0008053", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008053", "name": "MYP2", "description": "" }, { "id": "MONDO:0008053", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008053", "name": "myopia 2, autosomal dominant", "description": "" }, { "id": "MONDO:0013603", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013603", "name": "myopia 20, autosomal dominant", "description": "" }, { "id": "MONDO:0013603", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013603", "name": "MYP20", "description": "" }, { "id": "MONDO:0013603", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013603", "name": "myopia 20, autosomal dominant", "description": "" }, { "id": "MONDO:0013508", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013508", "name": "myopia 19, autosomal dominant", "description": "" }, { "id": "MONDO:0013508", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013508", "name": "MYP19", "description": "" }, { "id": "MONDO:0013508", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0013508", "name": "myopia 19, autosomal dominant", "description": "" }, { "id": "MONDO:0012932", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012932", "name": "myopia 16, autosomal dominant", "description": "" }, { "id": "MONDO:0012932", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012932", "name": "MYP16", "description": "" }, { "id": "MONDO:0012932", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012932", "name": "myopia 16", "description": "" }, { "id": "MONDO:0012932", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0012932", "name": "myopia 16, autosomal dominant", "description": "" }, { "id": "MIM:614167", "resource": "MIM", "url": "https://www.omim.org/entry/614167", "name": "Myopia 21, autosomal dominant", "description": "Myopia 21, autosomal dominant" }, { "id": "MIM:615420", "resource": "MIM", "url": "https://www.omim.org/entry/615420", "name": "Myopia 22, autosomal dominant", "description": "Myopia 22, autosomal dominant" }, { "id": "MIM:615946", "resource": "MIM", "url": "https://www.omim.org/entry/615946", "name": "Myopia 24, autosomal dominant", "description": "Myopia 24, autosomal dominant" }, { "id": "MIM:615431", "resource": "MIM", "url": "https://www.omim.org/entry/615431", "name": "Myopia 23, autosomal recessive", "description": "Myopia 23, autosomal recessive" }, { "id": "MIM:608908", "resource": "MIM", "url": "https://www.omim.org/entry/608908", "name": "Myopia 6", "description": "Myopia 6" } ], "evidence": [ { "id": "11830", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:11830" } ] }, { "disease_id": "DOID:1591", "recommended_name": { "id": "DOID:1591", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:1591", "name": "renovascular hypertension", "description": "" }, "synonyms": [], "evidence": [ { "id": "1591", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:1591" } ] }, { "disease_id": "DOID:9884", "recommended_name": { "id": "DOID:9884", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:9884", "name": "muscular dystrophy", "description": "A myopathy is characterized by progressive skeletal muscle weakness degeneration." }, "synonyms": [ { "id": "MONDO:0010678", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010678", "name": "muscular dystrophy, progressive Pectorodorsal", "description": "" }, { "id": "MONDO:0010678", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010678", "name": "muscular dystrophy, progressive Pectorodorsal", "description": "" }, { "id": "MONDO:0010678", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010678", "name": "muscular dystrophy, progressive, involving shoulder girdle and back", "description": "" }, { "id": "MONDO:0010884", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010884", "name": "muscular dystrophy, scapulohumeral", "description": "" }, { "id": "MONDO:0010884", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010884", "name": "muscular dystrophy, scapulohumeral", 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"https://www.alliancegenome.org/disease/DOID:9884" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Drosophila melanogaster", "taxid": 7227, "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" } ], "common_name": "Fruit fly" } ], "gene": [ { "name": "wb", "url": "https://www.uniprot.org/uniprot/Q8IP51", "locus": { "chromosome": "2L", "start_pos": 14328262, "end_pos": 14263027, "strand": "-", "evidence": [ { "database": "Ensembl Gene", "id": "FBgn0261563", "url": "https://www.ensembl.org/id/FBgn0261563" } ] } } ], "crossref": [ { "id": "FBgn0261563", "url": "https://bgee.org/?page=gene&gene_id=FBgn0261563", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "cd00055", "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00055", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "cd00110", "url": 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"PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR10574:SF439", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10574:SF439", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF00052", "url": "http://pfam.xfam.org/family/PF00052", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00053", "url": "http://pfam.xfam.org/family/PF00053", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00054", "url": "http://pfam.xfam.org/family/PF00054", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00055", "url": "http://pfam.xfam.org/family/PF00055", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF02210", "url": "http://pfam.xfam.org/family/PF02210", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "NP_723870", "url": "https://www.ncbi.nlm.nih.gov/protein/NP_723870", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "M9MRU0-1", "url": "https://www.uniprot.org/uniprot/M9MRU0-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "Q8IP51-1", "url": "https://www.uniprot.org/uniprot/Q8IP51-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "R9PY40-1", "url": "https://www.uniprot.org/uniprot/R9PY40-1", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MQIGNFIKWPLGLILILLVTHCQAKRQRKRLRGFSTAKDLQDYSMPLNDNSTELQQNIVSWTGARIASSPDKKKKSPQSSRRHKTKSGLIIESNIADSESMLAIASSESVTKKKPPQRRRNGKLQKSGGGAGGGALRLLKTEDVYSSSFSGGLYPPLFNVVPRAQISVNATCGQNGAEEYCKQVGAKPCGICNAHSSDRAKQRSIQSLISSGSGSGSGSGFEEGWWQSPTLQGGRQFEYVTILLDLKQTFQIFSVWLKSANSPRPASWILEKSLDGINFEPWQYFGLSDADCQRRWNLSGQNGKYVFQNDTEIICSTQFSKPGPLENGVLHASLLKNRPGATDQSPELMKFITTRYIRIRLQGMHSTANQDNSLDWLLDSPSLEKHSFYSLSQLKVSARLDCNGHANRSHESPDDPLMQCICQHNTCGAQCEQCCPLFQDRPYQMGGECEICQCYGHAESCTYDPFLDKGICQSCSNNTAGIECEFCEMGFYRELDAPLTDPCLPCSCNPARSTGGCQSDGGSCNCLEGFQGKNCEECAPGYYGDDCKRCECDERGSLGSTGSCSGVCQCKLNVEGSTCSECAPGYFDLSAENAEGCTSCWCSGVSQTCHSAKLQTLAFETLNDWKITDIQRVKPISIPVDAETNRLIFANELDEVEAIYWQASLGYLGNRLTSYGSRLQLVLSWDVIRGDRSGKPTTGPNVILVGKNGLKIAFGDESLDGLGINLNVTLTEVGWYHVPPTVVDIKTRLRRTEGGDYHGESVTRSQFLSVLVSLDAVLIRAAFHTDQGETSLERAVIYSGGVELGGKSSSQVEQCLCPAGYTGLSCEGCAFGFKRIYENTSDHQILSKCIPCPCNGHSNSCDLQSGNCGDCMHNTFGDRCERCQLGYYGNPLQGTPNDCKRCACPLSEDSNNFSPSCQLKSYNYMDLNPQFELIEHAEYICTQCPEGYTGDHCQVCDDGYFGNPRQPGSSCQRCDCAGGPCNVTTGECITCRGNTEGWHCERCKLGYWGDPAVGCDPCHCHTEGSESGLCDSTDGQCLCKPRYAGQKCDECDVGYANVELRCPSCNCDPLGSLVQDRCDPHTGQCHCKEGVMGAKCHECQDGYFGMNAVAYRMDDLAALRQNSDSDDDEWELVPDTEDPNSESTVACEECHCSSVGSLSSDCDKRTGQCACLANVTGRRCDKCRPGHWNLTAGEGCRDCRCDPHGSRGHECNPWTGQCDCKIGVGGQHCNECTEGFFGFSTEGCQRCSACRSEGQVCDPHNGRCICPKFTRGLGCGQCVPGTWGWQARLGCRECECDHIGSIGQQCSTGDGQCQCREGYSGRKCDTCAIGYFGYPECRRCGCDAEGSFTQADGSIACDSNGQCPCKSLVVGLKCDTCMQSTFGLSAQNPEGCTRCFCFGRSGECEQSDLSWGHIRMAESRNLSVQQIRPHSVPSSDYEYIVVVQMEGSSFHREDAEIQRMNDLSLVPKSTGNVSIGAYGQFYHPLYFQLPPQFYGDRTSSYGGFLYFTLITEGAHKPLERNILGQYPLVQLHAHSKLLLDFYEYEEFEYSLNVTHRVPLHESFWKYHHTSQAVDRNTLMAALQNIRHIFIRAFAFADFQEVVLQNVHMDAAIYIKGSTNLIAKGVERCKCPKRFDGLSCQDPGRSFYRWRNTTIVESVFIEDLIGRAAPCHCNGRSSDCDRETGVCQNCRGNTGGDHCHQCAEGFYGDPNSPHGCQACPCPETNRNFARGCNVWDGEVSCVCKPGYTGRLCERCQAGYFGDPMRYPNTTCQPCNCHPDGIQTEGCDVETGRCYCREGVTGLKCDKCQAERHHLVDNGCKICDNCTLLLLDYMELVGNKLRRGMHNMDLTGIPAPYRKLSEYESAYEKWNGRHWDFSQTKRRLQDYDSADILKLEAHAENLKFQSRKAVATIGKREFAIKSMREDAVTQQHSVGLLRSEILQTLSDLHGYGKSAHYLSLPTALKQARFYLQAIREHDQMVQGIRSTNDCAWKHFYAMGNASDASFDESGRLEMLWRDLNQTNHRVVDMRLQVDRVQEVENEAEDVLEHVRNLSIRVGESHQELDELNQRISDHLDPGYLEQGEGLLRLTVQRQIMLNGHLNQLDGYRILLNTTLGVKTEQQREVRKHWLPKAEKHASHLLARSNEYARKFQPTRNGARIAMLASSAHSNITEAINDARLASILAKERVYEAQRTLYPSDGSSMIERAKHSLHRSKQLQQEALKQMHKSNVLKDKLHRQEQQVEGIKSTIYDSGLRTNNISGQLQGLSDGSARRQAKDSLEMADRTGEQMRAELQKAKDMQKSIQNMRNSFSNLEPDWEIKLGMAQENISLTQTNLRLANVSLSYLEQQAEKEQQVFEVWNNSMAQQLQQLRDQIAKARHAAEAIDVSLESLGPKCIRSYLPASYGLSTSNKIRMSFALSNHLESSPLIHLASSEGRHITLELYKRRVRLVWNLGGTTATVTHPMVVHTRDPKYDDAWYHVEANRTLNLGSLVVRRMNNYGELTPPNPVIITGSTDTEHTRFYQSRSDRISLGGFASKDLQFTPGLNVVVHQVEVDNKPLGLWNFVTSEGSCGGSMVGAKESSASSTARHFNGLGYAQLMKTRPRPTRKNLFSVQMTFRTLDENALLFLAVDDKNNRSVSVTLSRGRIMFRIDYGDESKLEINTTKKYNVGQWIKIEAAREFSAKRSTENGMLRVNNDRPISGAPTLPVNIHLLPDLSKTVYYLGGVPPGFTSGTSKAPGADNPFLGCMKDVQVNGETYDPLESSSYYGVEPSCKNMITKAGFSGNGYLELPSQSLRKRSNTALVFRTLQPDCLLLLAAYPPEILGDYDAKDIKGNFSISLVDGQLHVWVNSGRSFIKMSSNSSQMNDGEFHVVHLIKTGRKLELMVDDELQEIRNLNGNPTVVSLPRDAGGLYIGGAPPHESYTPLAPTFVNLEGAIRDVVFNNRTINFNDALTFANVQIGRNGPLMGSLKGGLYDVLLKTEPMIGKSFTASPEGCKRIGSYSYEPNAFKFGDDIYSYSQLKLPERHFWQRNFHLSFDFRSFYPNGMLYLSPGSKEKPKHYVALVLKDGQLVLVVRGRRREELQLTAKLNDGEWHRVTISCHDRKVTMSVEIGRTDQKTSAQMKLPKKIGASQLLLVGGLPQSPVKVSSDLYVRLEPFKGCLRRVSINNNTQDLARPGKHSNVGQCFPTVERGSYFPGDAYAIYKKNFNVGKYLDLETEFRTSELSGILLSVSDPNGFPALSLELHNGNIIFSCDPGNGAPMRVESSLPTKYALCDNKWHNISALYDGEQIVLRIDQLPAVISVGNQGNAGKVQTRSPLYIGGLPESAPSGSLISRENFKGCIRHVSIRNERRDWIEMEDLRNVLLSECLVSSDES", "length": 3375, "header": "tr|Q8IP51-1|Q8IP51_DROME Isoform 1 of Wing blister, isoform B OS=Drosophila melanogaster OX=7227 GN=wb PE=4 SV=1 CANONICAL=Q8IP51-1" }, "isoforms": [ { "isoform_ac": "M9MRU0-1", "url": "", "sequence": { "sequence": "MSASDKRTVKMSDASIKPRKLKKHLRAADVKPRGMMTKSLLLHLCVYLVCITQTLQLQQRQQQQQQQHRQQQHGQPEGNMLQQHHRTSVNSSVNINISRQFNEIIQTATASASASGTGSASGAVTFASVTAATTITPGRRKLRRKFQGQQNRNSTLGRRRKLRLHPYHRRNATHATRTTTVASVSATATTLLPKMPHKQPFNYHTHLHSSFQQQQQQQHVAGGQVTQQQQQQQQVHVVAVTPRPQQRQQQPGFAIVPATYYHQQQQQQQRTLLGNLTQQQQQQQQHLLIQPGQNILVYSNLGPIPPCPPGLLSGSGMPVYTQQQHFIPLRSTTTPRPRQRECHCSSVGSLSSDCDKRTGQCACLANVTGRRCDKCRPGHWNLTAGEGCRDCRCDPHGSRGHECNPWTGQCDCKIGVGGQHCNECTEGFFGFSTEGCQRCSACRSEGQVCDPHNGRCICPKFTRGLGCGQCVPGTWGWQARLGCRECECDHIGSIGQQCSTGDGQCQCREGYSGRKCDTCAIGYFGYPECRRCGCDAEGSFTQADGSIACDSNGQCPCKSLVVGLKCDTCMQSTFGLSAQNPEGCTRCFCFGRSGECEQSDLSWGHIRMAESRNLSVQQIRPHSVPSSDYEYIVVVQMEGSSFHREDAEIQRMNDLSLVPKSTGNVSIGAYGQFYHPLYFQLPPQFYGDRTSSYGGFLYFTLITEGAHKPLERNILGQYPLVQLHAHSKLLLDFYEYEEFEYSLNVTHRVPLHESFWKYHHTSQAVDRNTLMAALQNIRHIFIRAFAFADFQEVVLQNVHMDAAIYIKGSTNLIAKGVERCKCPKRFDGLSCQDPGRSFYRWRNTTIVESVFIEDLIGRAAPCHCNGRSSDCDRETGVCQNCRGNTGGDHCHQCAEGFYGDPNSPHGCQACPCPETNRNFARGCNVWDGEVSCVCKPGYTGRLCERCQAGYFGDPMRYPNTTCQPCNCHPDGIQTEGCDVETGRCYCREGVTGLKCDKCQAERHHLVDNGCKICDNCTLLLLDYMELVGNKLRRGMHNMDLTGIPAPYRKLSEYESAYEKWNGRHWDFSQTKRRLQDYDSADILKLEAHAENLKFQSRKAVATIGKREFAIKSMREDAVTQQHSVGLLRSEILQTLSDLHGYGKSAHYLSLPTALKQARFYLQAIREHDQMVQGIRSTNDCAWKHFYAMGNASDASFDESGRLEMLWRDLNQTNHRVVDMRLQVDRVQEVENEAEDVLEHVRNLSIRVGESHQELDELNQRISDHLDPGYLEQGEGLLRLTVQRQIMLNGHLNQLDGYRILLNTTLGVKTEQQREVRKHWLPKAEKHASHLLARSNEYARKFQPTRNGARIAMLASSAHSNITEAINDARLASILAKERVYEAQRTLYPSDGSSMIERAKHSLHRSKQLQQEALKQMHKSNVLKDKLHRQEQQVEGIKSTIYDSGLRTNNISGQLQGLSDGSARRQAKDSLEMADRTGEQMRAELQKAKDMQKSIQNMRNSFSNLEPDWEIKLGMAQENISLTQTNLRLANVSLSYLEQQAEKEQQVFEVWNNSMAQQLQQLRDQIAKARHAAEAIDVSLESLGPKCIRSYLPASYGLSTSNKIRMSFALSNHLESSPLIHLASSEGRHITLELYKRRVRLVWNLGGTTATVTHPMVVHTRDPKYDDAWYHVEANRTLNLGSLVVRRMNNYGELTPPNPVIITGSTDTEHTRFYQSRSDRISLGGFASKDLQFTPGLNVVVHQVEVDNKPLGLWNFVTSEGSCGGSMVGAKESSASSTARHFNGLGYAQLMKTRPRPTRKNLFSVQMTFRTLDENALLFLAVDDKNNRSVSVTLSRGRIMFRIDYGDESKLEINTTKKYNVGQWIKIEAAREFSAKRSTENGMLRVNNDRPISGAPTLPVNIHLLPDLSKTVYYLGGVPPGFTSGTSKAPGADNPFLGCMKDVQVNGETYDPLESSSYYGVEPSCKNMITKAGFSGNGYLELPSQSLRKRSNTALVFRTLQPDCLLLLAAYPPEILGDYDAKDIKGNFSISLVDGQLHVWVNSGRSFIKMSSNSSQMNDGEFHVVHLIKTGRKLELMVDDELQEIRNLNGNPTVVSLPRDAGGLYIGGAPPHESYTPLAPTFVNLEGAIRDVVFNNRTINFNDALTFANVQIGRNGPLMGSLKGGLYDVLLKTEPMIGKSFTASPEGCKRIGSYSYEPNAFKFGDDIYSYSQLKLPERHFWQRNFHLSFDFRSFYPNGMLYLSPGSKEKPKHYVALVLKDGQLVLVVRGRRREELQLTAKLNDGEWHRVTISCHDRKVTMSVEIGRTDQKTSAQMKLPKKIGASQLLLVGGLPQSPVKVSSDLYVRLEPFKGCLRRVSINNNTQDLARPGKHSNVGQCFPTVERGSYFPGDAYAIYKKNFNVGKYLDLETEFRTSELSGILLSVSDPNGFPALSLELHNGNIIFSCDPGNGAPMRVESSLPTKYALCDNKWHNISALYDGEQIVLRIDQLPAVISVGNQGNAGKVQTRSPLYIGGLPESAPSGSLISRENFKGCIRHVSIRNERRDWIEMEDLRNVLLSECLVSSDES", "length": 2567, "header": "tr|M9MRU0-1|M9MRU0_DROME Computationally mapped isoform of Wing blister, isoform E OS=Drosophila melanogaster OX=7227 GN=wb PE=4 SV=1 CANONICAL=Q8IP51-1" }, "locus": { "chromosome": "2L", "start_pos": 14327748, "end_pos": 14308157, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "FBtr0302732", "url": "https://www.ensembl.org/id/FBtr0302732" }, { "database": "Ensembl Peptide", "id": "FBpp0291872", "url": "https://www.ensembl.org/id/FBpp0291872" } ] } }, { "isoform_ac": "Q8IP51-1", "url": "", "sequence": { "sequence": "MQIGNFIKWPLGLILILLVTHCQAKRQRKRLRGFSTAKDLQDYSMPLNDNSTELQQNIVSWTGARIASSPDKKKKSPQSSRRHKTKSGLIIESNIADSESMLAIASSESVTKKKPPQRRRNGKLQKSGGGAGGGALRLLKTEDVYSSSFSGGLYPPLFNVVPRAQISVNATCGQNGAEEYCKQVGAKPCGICNAHSSDRAKQRSIQSLISSGSGSGSGSGFEEGWWQSPTLQGGRQFEYVTILLDLKQTFQIFSVWLKSANSPRPASWILEKSLDGINFEPWQYFGLSDADCQRRWNLSGQNGKYVFQNDTEIICSTQFSKPGPLENGVLHASLLKNRPGATDQSPELMKFITTRYIRIRLQGMHSTANQDNSLDWLLDSPSLEKHSFYSLSQLKVSARLDCNGHANRSHESPDDPLMQCICQHNTCGAQCEQCCPLFQDRPYQMGGECEICQCYGHAESCTYDPFLDKGICQSCSNNTAGIECEFCEMGFYRELDAPLTDPCLPCSCNPARSTGGCQSDGGSCNCLEGFQGKNCEECAPGYYGDDCKRCECDERGSLGSTGSCSGVCQCKLNVEGSTCSECAPGYFDLSAENAEGCTSCWCSGVSQTCHSAKLQTLAFETLNDWKITDIQRVKPISIPVDAETNRLIFANELDEVEAIYWQASLGYLGNRLTSYGSRLQLVLSWDVIRGDRSGKPTTGPNVILVGKNGLKIAFGDESLDGLGINLNVTLTEVGWYHVPPTVVDIKTRLRRTEGGDYHGESVTRSQFLSVLVSLDAVLIRAAFHTDQGETSLERAVIYSGGVELGGKSSSQVEQCLCPAGYTGLSCEGCAFGFKRIYENTSDHQILSKCIPCPCNGHSNSCDLQSGNCGDCMHNTFGDRCERCQLGYYGNPLQGTPNDCKRCACPLSEDSNNFSPSCQLKSYNYMDLNPQFELIEHAEYICTQCPEGYTGDHCQVCDDGYFGNPRQPGSSCQRCDCAGGPCNVTTGECITCRGNTEGWHCERCKLGYWGDPAVGCDPCHCHTEGSESGLCDSTDGQCLCKPRYAGQKCDECDVGYANVELRCPSCNCDPLGSLVQDRCDPHTGQCHCKEGVMGAKCHECQDGYFGMNAVAYRMDDLAALRQNSDSDDDEWELVPDTEDPNSESTVACEECHCSSVGSLSSDCDKRTGQCACLANVTGRRCDKCRPGHWNLTAGEGCRDCRCDPHGSRGHECNPWTGQCDCKIGVGGQHCNECTEGFFGFSTEGCQRCSACRSEGQVCDPHNGRCICPKFTRGLGCGQCVPGTWGWQARLGCRECECDHIGSIGQQCSTGDGQCQCREGYSGRKCDTCAIGYFGYPECRRCGCDAEGSFTQADGSIACDSNGQCPCKSLVVGLKCDTCMQSTFGLSAQNPEGCTRCFCFGRSGECEQSDLSWGHIRMAESRNLSVQQIRPHSVPSSDYEYIVVVQMEGSSFHREDAEIQRMNDLSLVPKSTGNVSIGAYGQFYHPLYFQLPPQFYGDRTSSYGGFLYFTLITEGAHKPLERNILGQYPLVQLHAHSKLLLDFYEYEEFEYSLNVTHRVPLHESFWKYHHTSQAVDRNTLMAALQNIRHIFIRAFAFADFQEVVLQNVHMDAAIYIKGSTNLIAKGVERCKCPKRFDGLSCQDPGRSFYRWRNTTIVESVFIEDLIGRAAPCHCNGRSSDCDRETGVCQNCRGNTGGDHCHQCAEGFYGDPNSPHGCQACPCPETNRNFARGCNVWDGEVSCVCKPGYTGRLCERCQAGYFGDPMRYPNTTCQPCNCHPDGIQTEGCDVETGRCYCREGVTGLKCDKCQAERHHLVDNGCKICDNCTLLLLDYMELVGNKLRRGMHNMDLTGIPAPYRKLSEYESAYEKWNGRHWDFSQTKRRLQDYDSADILKLEAHAENLKFQSRKAVATIGKREFAIKSMREDAVTQQHSVGLLRSEILQTLSDLHGYGKSAHYLSLPTALKQARFYLQAIREHDQMVQGIRSTNDCAWKHFYAMGNASDASFDESGRLEMLWRDLNQTNHRVVDMRLQVDRVQEVENEAEDVLEHVRNLSIRVGESHQELDELNQRISDHLDPGYLEQGEGLLRLTVQRQIMLNGHLNQLDGYRILLNTTLGVKTEQQREVRKHWLPKAEKHASHLLARSNEYARKFQPTRNGARIAMLASSAHSNITEAINDARLASILAKERVYEAQRTLYPSDGSSMIERAKHSLHRSKQLQQEALKQMHKSNVLKDKLHRQEQQVEGIKSTIYDSGLRTNNISGQLQGLSDGSARRQAKDSLEMADRTGEQMRAELQKAKDMQKSIQNMRNSFSNLEPDWEIKLGMAQENISLTQTNLRLANVSLSYLEQQAEKEQQVFEVWNNSMAQQLQQLRDQIAKARHAAEAIDVSLESLGPKCIRSYLPASYGLSTSNKIRMSFALSNHLESSPLIHLASSEGRHITLELYKRRVRLVWNLGGTTATVTHPMVVHTRDPKYDDAWYHVEANRTLNLGSLVVRRMNNYGELTPPNPVIITGSTDTEHTRFYQSRSDRISLGGFASKDLQFTPGLNVVVHQVEVDNKPLGLWNFVTSEGSCGGSMVGAKESSASSTARHFNGLGYAQLMKTRPRPTRKNLFSVQMTFRTLDENALLFLAVDDKNNRSVSVTLSRGRIMFRIDYGDESKLEINTTKKYNVGQWIKIEAAREFSAKRSTENGMLRVNNDRPISGAPTLPVNIHLLPDLSKTVYYLGGVPPGFTSGTSKAPGADNPFLGCMKDVQVNGETYDPLESSSYYGVEPSCKNMITKAGFSGNGYLELPSQSLRKRSNTALVFRTLQPDCLLLLAAYPPEILGDYDAKDIKGNFSISLVDGQLHVWVNSGRSFIKMSSNSSQMNDGEFHVVHLIKTGRKLELMVDDELQEIRNLNGNPTVVSLPRDAGGLYIGGAPPHESYTPLAPTFVNLEGAIRDVVFNNRTINFNDALTFANVQIGRNGPLMGSLKGGLYDVLLKTEPMIGKSFTASPEGCKRIGSYSYEPNAFKFGDDIYSYSQLKLPERHFWQRNFHLSFDFRSFYPNGMLYLSPGSKEKPKHYVALVLKDGQLVLVVRGRRREELQLTAKLNDGEWHRVTISCHDRKVTMSVEIGRTDQKTSAQMKLPKKIGASQLLLVGGLPQSPVKVSSDLYVRLEPFKGCLRRVSINNNTQDLARPGKHSNVGQCFPTVERGSYFPGDAYAIYKKNFNVGKYLDLETEFRTSELSGILLSVSDPNGFPALSLELHNGNIIFSCDPGNGAPMRVESSLPTKYALCDNKWHNISALYDGEQIVLRIDQLPAVISVGNQGNAGKVQTRSPLYIGGLPESAPSGSLISRENFKGCIRHVSIRNERRDWIEMEDLRNVLLSECLVSSDES", "length": 3375, "header": "tr|Q8IP51-1|Q8IP51_DROME Isoform 1 of Wing blister, isoform B OS=Drosophila melanogaster OX=7227 GN=wb PE=4 SV=1 CANONICAL=Q8IP51-1" }, "locus": { "chromosome": "2L", "start_pos": 14327748, "end_pos": 14263721, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "FBtr0302731", "url": "https://www.ensembl.org/id/FBtr0302731" }, { "database": "Ensembl Peptide", "id": "FBpp0291871", "url": "https://www.ensembl.org/id/FBpp0291871" } ] } }, { "isoform_ac": "R9PY40-1", "url": "", "sequence": { "sequence": "MQIGNFIKWPLGLILILLVTHCQAKRQRKRLRGFSTAKDLQDYSMPLNDNSTELQQNIVSWTGARIASSPDKKKKSPQSSRRHKTKSGLIIESNIADSESMLAIASSESVTKKKPPQRRRNGKLQKSGGGAGGGALRLLKTEDVYSSSFSGGLYPPLFNVVPRAQISVNATCGQNGAEEYCKQVGAKPCGICNAHSSDRAKQRSIQSLISSGSGSGSGSGFEEGWWQSPTLQGGRQFEYVTILLDLKQTFQIFSVWLKSANSPRPASWILEKSLDGINFEPWQYFGLSDADCQRRWNLSGQNGKYVFQNDTEIICSTQFSKPGPLENGVLHASLLKNRPGATDQSPELMKFITTRYIRIRLQGMHSTANQDNSLDWLLDSPSLEKHSFYSLSQLKVSARLDCNGHANRSHESPDDPLMQCICQHNTCGAQCEQCCPLFQDRPYQMGGECEICQCYGHAESCTYDPFLDKGICQSCSNNTAGIECEFCEMGFYRELDAPLTDPCLPCSCNPARSTGGCQSDGGSCNCLEGFQGKNCEECAPGYYGDDCKRCECDERGSLGSTGSCSGVCQCKLNVEGSTCSECAPGYFDLSAENAEGCTSCWCSGVSQTCHSAKLQTLAFETLNDWKITDIQRVKPISIPVDAETNRLIFANELDEVEAIYWQASLGYLGNRLTSYGSRLQLVLSWDVIRGDRSGKPTTGPNVILVGKNGLKIAFGDESLDGLGINLNVTLTEVGWYHVPPTVVDIKTRLRRTEGGDYHGESVTRSQFLSVLVSLDAVLIRAAFHTDQGETSLERAVIYSGGVELGGKSSSQVEQCLCPAGYTGLSCEGCAFGFKRIYENTSDHQILSKCIPCPCNGHSNSCDLQSGNCGDCMHNTFGDRCERCQLGYYGNPLQGTPNDCKRCACPLSEDSNNFSPSCQLKSYNYMDLNPQFELIEHAEYICTQCPEGYTGDHCQVCDDGYFGNPRQPGSSCQRCDCAGGPCNVTTGECITCRGNTEGWHCERCKLGYWGDPAVGCDPCHCHTEGSESGLCDSTDGQCLCKPRYAGQKCDECDVGYANVELRCPSCNCDPLGSLVQDRCDPHTGQCHCKEGVMGAKCHECQDGYFGMNAVAYRMDDLAALRQNSDSDDDEWELVPDTEDPNSESTVACEECHCSSVGSLSSDCDKRTGQCACLANVTGRRCDKCRPGHWNLTAGEGCRDCRCDPHGSRGHECNPWTGQCDCKIGVGGQHCNECTEGFFGFSTEGCQRCSACRSEGQVCDPHNGRCICPKFTRGLGCGQCVPGTWGWQARLGCRECECDHIGSIGQQCSTGDGQCQCREGYSGRKCDTCAIGYFGYPECRRCGCDAEGSFTQADGSIACDSNGQCPCKSLVVGLKCDTCMQSTFGLSAQNPEGCTRCFCFGRSGECEQSDLSWGHIRMAESRNLSVQQIRPHSVPSSDYEYIVVVQMEGSSFHREDAEIQRMNDLSLVPKSTGNVSIGAYGQFYHPLYFQLPPQFYGDRTSSYGGFLYFTLITEGAHKPLERNILGQYPLVQLHAHSKLLLDFYEYEEFEYSLNVTHRVPLHESFWKYHHTSQAVDRNTLMAALQNIRHIFIRAFAFADFQEVVLQNVHMDAAIYIKGSTNLIAKGVERCKCPKRFDGLSCQDPGRSFYRWRNTTIVESVFIEDLIGRAAPCHCNGRSSDCDRETGVCQNCRGNTGGDHCHQCAEGFYGDPNSPHGCQACPCPETNRNFARGCNVWDGEVSCVCKPGYTGRLCERCQAGYFGDPMRYPNTTCQPCNCHPDGIQTEGCDVETGRCYCREGVTGLKCDKCQAERHHLVDNGCKICDNCTLLLLDYMELVGNKLRRGMHNMDLTGIPAPYRKLSEYESAYEKWNGRHWDFSQTKRRLQDYDSADILKLEAHAENLKFQSRKAVATIGKREFAIKSMREDAVTQQHSVGLLRSEILQTLSDLHGYGKSAHYLSLPTALKQARFYLQAIREHDQMVQGIRSTNDCAWKHFYAMGNASDASFDESGRLEMLWRDLNQTNHRVVDMRLQVDRVQEVENEAEDVLEHVRNLSIRVGESHQELDELNQRISDHLDPGYLEQGEGLLRLTVQRQIMLNGHLNQLDGYRILLNTTLGVKTEQQREVRKHWLPKAEKHASHLLARSNEYARKFQPTRNGARIAMLASSAHSNITEAINDARLASILAKERVYEAQRTLYPSDGSSMIERAKHSLHRSKQLQQEALKQMHKSNVLKDKLHRQEQQVEGIKSTIYDSGLRTNNISGQLQGLSDGSARRQAKDSLEMADRTGEQMRAELQKAKDMQKSIQNMRNSFSNLEPDWEIKLGMAQENISLTQTNLRLANVSLSYLEQQAEKEQQVFEVWNNSMAQQLQQLRDQIAKARHAAEAIDVSLESLGPKCIRSYLPASYGLSTSNKIRMSFALSNHLESSPLIHLASSEGRHITLELYKRRVRLVWNLGGTTATVTHPMVVHTRDPKYDDAWYHVEANRTLNLGSLVVRRMNNYGELTPPNPVIITGSTDTEHTRFYQSRSDRISLGGFASKDLQFTPGLNVVVHQVEVDNKPLGLWNFVTSEGSCGGSMVGAKESSASSTARHFNGLGYAQLMKTRPRPTRKNLFSVQMTFRTLDENALLFLAVDDKNNRSVSVTLSRGRIMFRIDYGDESKLEINTTKKYNVGQWIKIEAAREFSAKRSTENGMLRVNNDRPISGAPTLPVNIHLLPDLSKTVYYLGGVPPGFTSGTSKAPGADNPFLGCMKDVQVNGETYDPLESSSYYGVEPSCKNMITKAGFSGNGYLELPSQSLRKRSNTALVFRTLQPDCLLLLAAYPPEILGDYDAKDIKGNFSISLVDGQLHVWVNSGRSFIKMSSNSSQMNDGEFHVVHLIKTGRKLELMVDDELQEIRNLNGNPTVVSLPRDAGGLYIGGAPPHESYTPLAPTFVNLEGAIRDVVFNNRTINFNDALTFANVQIGRNGPLMGSLKGGLYDVLLKTEPMIGKSFTASPEGCKRDFSC", "length": 3001, "header": "tr|R9PY40-1|R9PY40_DROME Computationally mapped isoform of Wing blister, isoform G OS=Drosophila melanogaster OX=7227 GN=wb PE=4 SV=1 CANONICAL=Q8IP51-1" }, "locus": { "chromosome": "2L", "start_pos": 14325707, "end_pos": 14263721, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "FBtr0305063", "url": "https://www.ensembl.org/id/FBtr0305063" }, { "database": "Ensembl Peptide", "id": "FBpp0293600", "url": "https://www.ensembl.org/id/FBpp0293600" } ] } } ], "glycosylation": [], "phosphorylation": [], "glycation": [], "keywords": [], "publication": [ { "title": "The genome sequence of Drosophila melanogaster.", "journal": "Science", "date": "2000", "authors": "Adams MD, Celniker SE, Holt RA, Evans CA, Gocayne JD, Amanatides PG, Scherer SE, Li PW, Hoskins RA, Galle RF, George RA, Lewis SE, Richards S, Ashburner M, Henderson SN, Sutton GG, Wortman JR, Yandell MD, Zhang Q, Chen LX, Brandon RC, Rogers YH, Blazej RG, Champe M, Pfeiffer BD, Wan KH, Doyle C, Baxter EG, Helt G, Nelson CR, Gabor GL, Abril JF, Agbayani A, An HJ, Andrews-Pfannkoch C, Baldwin D, Ballew RM, Basu A, Baxendale J, Bayraktaroglu L, Beasley EM, Beeson KY, Benos PV, Berman BP, Bhandari D, Bolshakov S, Borkova D, Botchan MR, Bouck J, Brokstein P, Brottier P, Burtis KC, Busam DA, Butler H, Cadieu E, Center A, Chandra I, Cherry JM, Cawley S, Dahlke C, Davenport LB, Davies P, de Pablos B, Delcher A, Deng Z, Mays AD, Dew I, Dietz SM, Dodson K, Doup LE, Downes M, Dugan-Rocha S, Dunkov BC, Dunn P, Durbin KJ, Evangelista CC, Ferraz C, Ferriera S, Fleischmann W, Fosler C, Gabrielian AE, Garg NS, Gelbart WM, Glasser K, Glodek A, Gong F, Gorrell JH, Gu Z, Guan P, Harris M, Harris NL, Harvey D, Heiman TJ, Hernandez JR, Houck J, Hostin D, Houston KA, Howland TJ, Wei MH, Ibegwam C, Jalali M, Kalush F, Karpen GH, Ke Z, Kennison JA, Ketchum KA, Kimmel BE, Kodira CD, Kraft C, Kravitz S, Kulp D, Lai Z, Lasko P, Lei Y, Levitsky AA, Li J, Li Z, Liang Y, Lin X, Liu X, Mattei B, McIntosh TC, McLeod MP, McPherson D, Merkulov G, Milshina NV, Mobarry C, Morris J, Moshrefi A, Mount SM, Moy M, Murphy B, Murphy L, Muzny DM, Nelson DL, Nelson DR, Nelson KA, Nixon K, Nusskern DR, Pacleb JM, Palazzolo M, Pittman GS, Pan S, Pollard J, Puri V, Reese MG, Reinert K, Remington K, Saunders RD, Scheeler F, Shen H, Shue BC, Siden-Kiamos I, Simpson M, Skupski MP, Smith T, Spier E, Spradling AC, Stapleton M, Strong R, Sun E, Svirskas R, Tector C, Turner R, Venter E, Wang AH, Wang X, Wang ZY, Wassarman DA, Weinstock GM, Weissenbach J, Williams SM, WoodageT, Worley KC, Wu D, Yang S, Yao QA, Ye J, Yeh RF, Zaveri JS, Zhan M, Zhang G, Zhao Q, Zheng L, Zheng XH, Zhong FN, Zhong W, Zhou X, Zhu S, Zhu X, Smith HO, Gibbs RA, Myers EW, Rubin GM, Venter JC", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "10731132", "url": "https://glygen.org/publication/PubMed/10731132" } ] }, { "title": "Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence.", "journal": "Genome Biol.", "date": "2002", "authors": "Celniker SE, Wheeler DA, Kronmiller B, Carlson JW, Halpern A, Patel S, Adams M, Champe M, Dugan SP, Frise E, Hodgson A, George RA, Hoskins RA, Laverty T, Muzny DM, Nelson CR, Pacleb JM, Park S, Pfeiffer BD, Richards S, Sodergren EJ, Svirskas R, Tabor PE, Wan K, Stapleton M, Sutton GG, Venter C, Weinstock G, Scherer SE, Myers EW, Gibbs RA, Rubin GM", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "12537568", "url": "https://glygen.org/publication/PubMed/12537568" } ] }, { "title": "Annotation of the Drosophila melanogaster euchromatic genome: a systematic review.", "journal": "Genome Biol.", "date": "2002", "authors": "Misra S, Crosby MA, Mungall CJ, Matthews BB, Campbell KS, Hradecky P, Huang Y, Kaminker JS, Millburn GH, Prochnik SE, Smith CD, Tupy JL, Whitfied EJ, Bayraktaroglu L, Berman BP, Bettencourt BR, Celniker SE, de Grey AD, Drysdale RA, Harris NL, Richter J, Russo S, Schroeder AJ, Shu SQ, Stapleton M, Yamada C, Ashburner M, Gelbart WM, Rubin GM, Lewis SE", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "12537572", "url": "https://glygen.org/publication/PubMed/12537572" } ] }, { "title": "The transposable elements of the Drosophila melanogaster euchromatin: a genomics perspective.", "journal": "Genome Biol.", "date": "2002", "authors": "Kaminker JS, Bergman CM, Kronmiller B, Carlson J, Svirskas R, Patel S, Frise E, Wheeler DA, Lewis SE, Rubin GM, Ashburner M, Celniker SE", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "12537573", "url": "https://glygen.org/publication/PubMed/12537573" } ] }, { "title": "Heterochromatic sequences in a Drosophila whole-genome shotgun assembly.", "journal": "Genome Biol.", "date": "2002", "authors": "Hoskins RA, Smith CD, Carlson JW, Carvalho AB, Halpern A, Kaminker JS, Kennedy C, Mungall CJ, Sullivan BA, Sutton GG, Yasuhara JC, Wakimoto BT, Myers EW, Celniker SE, Rubin GM, Karpen GH", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "12537574", "url": "https://glygen.org/publication/PubMed/12537574" } ] }, { "title": "Combined evidence annotation of transposable elements in genome sequences.", "journal": "PLoS Comput. Biol.", "date": "2005", "authors": "Quesneville H, Bergman CM, Andrieu O, Autard D, Nouaud D, Ashburner M, Anxolabehere D", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "16110336", "url": "https://glygen.org/publication/PubMed/16110336" } ] }, { "title": "The Release 5.1 annotation of Drosophila melanogaster heterochromatin.", "journal": "Science", "date": "2007", "authors": "Smith CD, Shu S, Mungall CJ, Karpen GH", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "17569856", "url": "https://glygen.org/publication/PubMed/17569856" } ] }, { "title": "Sequence finishing and mapping of Drosophila melanogaster heterochromatin.", "journal": "Science", "date": "2007", "authors": "Hoskins RA, Carlson JW, Kennedy C, Acevedo D, Evans-Holm M, Frise E, Wan KH, Park S, Mendez-Lago M, Rossi F, Villasante A, Dimitri P, Karpen GH, Celniker SE", "evidence": [ { "database": "UniProtKB", "id": "Q8IP51", "url": "https://www.uniprot.org/uniprot/Q8IP51" }, { "database": "UniProtKB", "id": "R9PY40", "url": "https://www.uniprot.org/uniprot/R9PY40" }, { "database": "UniProtKB", "id": "M9MRU0", "url": "https://www.uniprot.org/uniprot/M9MRU0" } ], "reference": [ { "type": "PubMed", "id": "17569867", "url": "https://glygen.org/publication/PubMed/17569867" } ] }, { "title": "The Release 6 reference sequence of the Drosophila melanogaster genome.", "journal": "Genome Res.", "date": 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