{ "uniprot_canonical_ac": "A0A0G2JWX2-1", "uniprot_ac": "A0A0G2JWX2", "uniprot_id": "A0A0G2JWX2_RAT", "mass": { "chemical_mass": 343928.0, "monoisotopic_mass": 343928.0 }, "refseq": {}, "gene_names": [ { "name": "Lama2", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2", "id": "A0A0G2JWX2" } ], "protein_names": [ { "name": "Laminin subunit alpha 2", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JWX2/entry#names_and_taxonomy", "id": "A0A0G2JWX2" } ], "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", "description": "" }, { "id": "MONDO:0010676", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010676", "name": "muscular dystrophy, Hemizygous lethal type", "description": "" }, { "id": "MONDO:0010676", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010676", "name": "muscular dystrophy, Hemizygous lethal type", "description": "" }, { "id": "MONDO:0010675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010675", "name": "muscular dystrophy, cardiac type", "description": "" }, { "id": "MONDO:0010675", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010675", "name": "muscular dystrophy, cardiac type", "description": "" }, { "id": "MONDO:0010677", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010677", "name": "muscular dystrophy, Mabry type", "description": "" }, { "id": "MONDO:0010677", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0010677", "name": "muscular dystrophy, Mabry type", "description": "" }, { "id": "MONDO:0008028", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008028", "name": "muscular dystrophy, Barnes type", "description": "" }, { "id": "MONDO:0008028", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008028", "name": "muscular dystrophy, Barnes type", "description": "" }, { "id": "MONDO:0008034", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008034", "name": "muscular dystrophy, pseudohypertrophic, with Internalized capillaries", "description": "" }, { "id": "MONDO:0008034", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0008034", "name": "muscular dystrophy, pseudohypertrophic, with Internalized capillaries", "description": "" } ], "evidence": [ { "id": "9884", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:9884" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Rattus norvegicus", "taxid": 10116, "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "common_name": "Rat", "glygen_name": "Rat", "reference_species": "Rattus norvegicus [10116]" } ], "gene": [ { "name": "Lama2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2", "locus": { "chromosome": "1", "start_pos": 18320530, "end_pos": 17672536, "strand": "-", "evidence": [ { "database": "Ensembl Gene", "id": "ENSRNOG00000011134", "url": "https://www.ensembl.org/id/ENSRNOG00000011134" } ] } } ], "crossref": [ { "id": "ENSRNOG00000011134", "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000011134", "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": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00110", "database": "CDD", "categories": [ "Protein Classification" ] }, { "id": "IPR000034", "url": "https://www.ebi.ac.uk/interpro/entry/IPR000034", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR000742", "url": "https://www.ebi.ac.uk/interpro/entry/IPR000742", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR001791", "url": "https://www.ebi.ac.uk/interpro/entry/IPR001791", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR002049", "url": "https://www.ebi.ac.uk/interpro/entry/IPR002049", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR008211", "url": "https://www.ebi.ac.uk/interpro/entry/IPR008211", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR009030", "url": "https://www.ebi.ac.uk/interpro/entry/IPR009030", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR009254", "url": "https://www.ebi.ac.uk/interpro/entry/IPR009254", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR010307", "url": "https://www.ebi.ac.uk/interpro/entry/IPR010307", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR013320", "url": "https://www.ebi.ac.uk/interpro/entry/IPR013320", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR050440", "url": "https://www.ebi.ac.uk/interpro/entry/IPR050440", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "SHSRINF", "url": "https://omabrowser.org/oma/group/SHSRINF/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "PTHR10574", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10574", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR10574:SF435", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR10574:SF435", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF00052", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF00052", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00053", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF00053", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00054", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF00054", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF00055", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF00055", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF02210", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF02210", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF06008", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF06008", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "PF06009", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF06009", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "XP_017445977", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_017445977", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "1308889", "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1308889", "database": "RGD", "categories": [ "Organism-specific" ] }, { "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A0G2JWX2-1", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A8I5ZPP7", "url": "https://www.uniprot.org/uniprot/A0A8I5ZPP7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A8I5ZPP7-1", "url": 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"MPAAGGILLLLLLGILEGSQTQRPQQRRQSPAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSHPYQRHPITNAIDGKNTWWQSPSIKNGVEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDEEYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPATNKSRCECEHNTCGESCDRCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDETVASRNLSLNIHGKYIGGGVCINCTHNTAGINCETCIDGFFRPKGVSPSYPRPCQPCHCDPAGSLSEVCIKDEKHTRRGLKPGSCYCKPGFGGMNCDRCVRGYRGYPDCQPCNCSGLGSTNQDPCIGPCSCKENVEGEDCSHCKFGFFNLQEENQKGCEECFCSGVSDRCQSSYWTYGNIQDMHGWYLTDLSGRIQVAPQLDNPDAPQQISVSNSEARRSLPDSYYWSAPAPYLRNKLPAVGGQLSFTISYDLEEEEDDTEKILQLMIILEGNNLRISTAYKEVHLEPSEEHVEELSLKEESFTIHGTNLPVSRKDFMILLTNLERVLIQTTYNLGMDVIFRLSSVNLESAVPYPTDRSIASAVEVCQCPPGYSGSSCEACWPRHRRVNGTIFGGLCEPCQCFGHAEACNDVTGECLSCKDHTGGPYCNECLPGFYGDPTRGTSEDCQPCACPLNIPSNNFSPTCHLDRSLGLICDECPVGYTGPRCERCAEGYFGQPSIPGGSCQPCLCNDNLDFSIPGSCDSLSGSCLICKPGTTGRFCELCADGYFGDAVDAKNCQPCRCNVNGSFSEICHRKTGQCECRPNVQGQRCDECKPETFGLQLGRGCIPCNCNSFGSKSFDCEASGQCWCQPGVAGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCNPKTGQCICPPNTIGEKCSECLPNTWGHSIVTGCKVCNCSTVGSLSSQCNINTGQCSCHPKFSGMKCSECNRGHWNYPLCSLCDCFLPGTDATTCDSETRKCSCSDQTGQCTCKVNVEGVHCDRCRPGKFGLEAKNPLGCSSCYCFGVTSQCSEAKGLVRTWVTLRDEQTILPLVDEALQHTTTKGIAFQNPEIVAKMDEVRQDLHLEPFYWKLPEQFEGKKLMAYGGKLKYTIYFEARDETGFATYKPQVIIRGGTPTHARIITRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRISRTVTREDFLDILYDIHYILIKATYGNVVRQSRISEISMEGAEPGQVSAASPLANLIERCDCPPGYSGLSCETCAPGFYRVHSEPGGRTPGPTLGTCVPCQCHGHSSQCDPETSVCQNCQHHTAGDFCERCALGYYGIVRGLPNDCQPCACPLISPSNNFSPSCVLEGLEDYRCTACPRGYEGQYCERCAPGYAGSPSSPGGSCQECECDPYGSLPVPCDPVTGLCTCRPGATGRKCDGCEHGHAREGAECVFCGDECTGLLLGDLAHLEQMAMNINLTGPLPAPYKILYGLENATQELKHLLSPQRAPERLLQLAEGNMNTLVMEMNELLTRATKVTADGEQTGQDAERTNSRAQSLEEFIKGLVQHAEAVNEKAIKLNETLGSQDRTAERNLQELQKEIDRMLKELRSKDLQTQKEVAEDELVAAEGLLKRVNKLFGEPRAQNEEMEKDLREKLAEYQNKLDDAWDLLREATKKTKDADRLSAANQKNMTILETKKEAIEGSKRQIENTLKEGNDILDEANRLAGEITSVIDYVEDIKTKLPPMSEELSDKIDDLAQEIKDRRLAEKVFQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFRAYSNIKDYIDEAEKVAREAKELAHEATKLATSPQGLLKEDAKGSLQKSFRILNEAKKLANDVKENHNDLSGLKTRLETADLRNSGLLGALNDTMDKLSAIPNDTAAKLQAVKEKAREANDTAKAVLAQVKDLHQNLDGLKQNYNKLADSVAKTNAVVKDPSKNKIIADAGATVRNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIVVHVKTAVADNLLFYLGSAKFIDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIEASRTGRNGSISVRALDGPKASMVPSTHHSVSPPGYTILDVDANAMLFVGGLTGKIKKADAVRVTTFTGCMGETYFDNKPIGLWNFREKEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSNALLMYLATRDLKDFMSVELSDGHVKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDSNQEENIATSSSGNNFGLDLKADDKIYFGGLPTLRNLSMKARPEVNVKKYSGCLKDIEISRTPYNILSSPNYVGVTKGCSLENVYTVSFPKPGFVELAAVSIDVGTEINLSFSTRNESGIILLGSGGTLTPPRRKRRQTTQAYYAIFLNKGRLEVHLSSGTRTMRKIVIKPEPNLFHDGREHSVHVERTRGVFTVQVDENRRHMQNLTEEQPIEVKKLFVGGAPPEFQPSPLRNIPAFQGCVWNLVINSIPMDFAQPIAFKNADIGRCAYQKPREEEDDAVPAEVTVQPQPVPTPAFPFPAPTMVHGPCVAESEPAFLSGSKQFGLSRNSHIALAFDDTKVKNRLTIELEVRTEAESGLLFYMARINHADFATVQLRNGFPYFSYDLGSGDTSTMIPTRINDGQWHKIKITRVKQEGILSVDDASNQTISPKKADILDVVGILYVGGLPINYTTRRIGPVTYSLDGCVRNLYMEQAPVDLDQPTSSFHVGTCFANAEKGTYFDGTGFAKAVGGFKVGLDLLVEFEFRTTRPTGVLLGVSSQKMDGMGIEMIDEKLMFHVDNGAGRFTAVYDAGSPGHMCDGRWHKVTAKKIKNRLELVVDGNQVDAQSPNAASTSADTNDPVFVGGFPDGLNQFGLTTNVRFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPTT", "length": 3121, "header": "tr|A0A0G2JWX2-1|A0A0G2JWX2_RAT Isoform 1 of Laminin subunit alpha 2 OS=Rattus norvegicus OX=10116 GN=Lama2 PE=1 SV=1 CANONICAL=A0A0G2JWX2-1" }, "isoforms": [ { "isoform_ac": "A0A0G2JWX2-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JWX2/entry#A0A0G2JWX2-1", "sequence": { "sequence": "MPAAGGILLLLLLGILEGSQTQRPQQRRQSPAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSHPYQRHPITNAIDGKNTWWQSPSIKNGVEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDEEYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPATNKSRCECEHNTCGESCDRCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDETVASRNLSLNIHGKYIGGGVCINCTHNTAGINCETCIDGFFRPKGVSPSYPRPCQPCHCDPAGSLSEVCIKDEKHTRRGLKPGSCYCKPGFGGMNCDRCVRGYRGYPDCQPCNCSGLGSTNQDPCIGPCSCKENVEGEDCSHCKFGFFNLQEENQKGCEECFCSGVSDRCQSSYWTYGNIQDMHGWYLTDLSGRIQVAPQLDNPDAPQQISVSNSEARRSLPDSYYWSAPAPYLRNKLPAVGGQLSFTISYDLEEEEDDTEKILQLMIILEGNNLRISTAYKEVHLEPSEEHVEELSLKEESFTIHGTNLPVSRKDFMILLTNLERVLIQTTYNLGMDVIFRLSSVNLESAVPYPTDRSIASAVEVCQCPPGYSGSSCEACWPRHRRVNGTIFGGLCEPCQCFGHAEACNDVTGECLSCKDHTGGPYCNECLPGFYGDPTRGTSEDCQPCACPLNIPSNNFSPTCHLDRSLGLICDECPVGYTGPRCERCAEGYFGQPSIPGGSCQPCLCNDNLDFSIPGSCDSLSGSCLICKPGTTGRFCELCADGYFGDAVDAKNCQPCRCNVNGSFSEICHRKTGQCECRPNVQGQRCDECKPETFGLQLGRGCIPCNCNSFGSKSFDCEASGQCWCQPGVAGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCNPKTGQCICPPNTIGEKCSECLPNTWGHSIVTGCKVCNCSTVGSLSSQCNINTGQCSCHPKFSGMKCSECNRGHWNYPLCSLCDCFLPGTDATTCDSETRKCSCSDQTGQCTCKVNVEGVHCDRCRPGKFGLEAKNPLGCSSCYCFGVTSQCSEAKGLVRTWVTLRDEQTILPLVDEALQHTTTKGIAFQNPEIVAKMDEVRQDLHLEPFYWKLPEQFEGKKLMAYGGKLKYTIYFEARDETGFATYKPQVIIRGGTPTHARIITRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRISRTVTREDFLDILYDIHYILIKATYGNVVRQSRISEISMEGAEPGQVSAASPLANLIERCDCPPGYSGLSCETCAPGFYRVHSEPGGRTPGPTLGTCVPCQCHGHSSQCDPETSVCQNCQHHTAGDFCERCALGYYGIVRGLPNDCQPCACPLISPSNNFSPSCVLEGLEDYRCTACPRGYEGQYCERCAPGYAGSPSSPGGSCQECECDPYGSLPVPCDPVTGLCTCRPGATGRKCDGCEHGHAREGAECVFCGDECTGLLLGDLAHLEQMAMNINLTGPLPAPYKILYGLENATQELKHLLSPQRAPERLLQLAEGNMNTLVMEMNELLTRATKVTADGEQTGQDAERTNSRAQSLEEFIKGLVQHAEAVNEKAIKLNETLGSQDRTAERNLQELQKEIDRMLKELRSKDLQTQKEVAEDELVAAEGLLKRVNKLFGEPRAQNEEMEKDLREKLAEYQNKLDDAWDLLREATKKTKDADRLSAANQKNMTILETKKEAIEGSKRQIENTLKEGNDILDEANRLAGEITSVIDYVEDIKTKLPPMSEELSDKIDDLAQEIKDRRLAEKVFQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFRAYSNIKDYIDEAEKVAREAKELAHEATKLATSPQGLLKEDAKGSLQKSFRILNEAKKLANDVKENHNDLSGLKTRLETADLRNSGLLGALNDTMDKLSAIPNDTAAKLQAVKEKAREANDTAKAVLAQVKDLHQNLDGLKQNYNKLADSVAKTNAVVKDPSKNKIIADAGATVRNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIVVHVKTAVADNLLFYLGSAKFIDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIEASRTGRNGSISVRALDGPKASMVPSTHHSVSPPGYTILDVDANAMLFVGGLTGKIKKADAVRVTTFTGCMGETYFDNKPIGLWNFREKEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSNALLMYLATRDLKDFMSVELSDGHVKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDSNQEENIATSSSGNNFGLDLKADDKIYFGGLPTLRNLSMKARPEVNVKKYSGCLKDIEISRTPYNILSSPNYVGVTKGCSLENVYTVSFPKPGFVELAAVSIDVGTEINLSFSTRNESGIILLGSGGTLTPPRRKRRQTTQAYYAIFLNKGRLEVHLSSGTRTMRKIVIKPEPNLFHDGREHSVHVERTRGVFTVQVDENRRHMQNLTEEQPIEVKKLFVGGAPPEFQPSPLRNIPAFQGCVWNLVINSIPMDFAQPIAFKNADIGRCAYQKPREEEDDAVPAEVTVQPQPVPTPAFPFPAPTMVHGPCVAESEPAFLSGSKQFGLSRNSHIALAFDDTKVKNRLTIELEVRTEAESGLLFYMARINHADFATVQLRNGFPYFSYDLGSGDTSTMIPTRINDGQWHKIKITRVKQEGILSVDDASNQTISPKKADILDVVGILYVGGLPINYTTRRIGPVTYSLDGCVRNLYMEQAPVDLDQPTSSFHVGTCFANAEKGTYFDGTGFAKAVGGFKVGLDLLVEFEFRTTRPTGVLLGVSSQKMDGMGIEMIDEKLMFHVDNGAGRFTAVYDAGSPGHMCDGRWHKVTAKKIKNRLELVVDGNQVDAQSPNAASTSADTNDPVFVGGFPDGLNQFGLTTNVRFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPTT", "length": 3121, "header": "tr|A0A0G2JWX2-1|A0A0G2JWX2_RAT Isoform 1 of Laminin subunit alpha 2 OS=Rattus norvegicus OX=10116 GN=Lama2 PE=1 SV=1 CANONICAL=A0A0G2JWX2-1" }, "locus": { "chromosome": "1", "start_pos": 18320424, "end_pos": 17672766, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000079138.2", "url": "https://www.ensembl.org/id/ENSRNOT00000079138.2" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000070049.2", "url": "https://www.ensembl.org/id/ENSRNOP00000070049.2" } ] } }, { "isoform_ac": "A0A8I5ZPP7-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JWX2/entry#A0A8I5ZPP7-1", "sequence": { "sequence": "MPAAGGILLLLLLGILEGSQTQRPQQRRQSPAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSHPYQRHPITNAIDGKNTWWQSPSIKNGVEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDEEYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPATNKSRCECEHNTCGESCDRCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDETVASRNLSLNIHGKYIGGGVCINCTHNTAGINCETCIDGFFRPKGVSPSYPRPCQPCHCDPAGSLSEVCIKDEKHTRRGLKPGSCYCKPGFGGMNCDRCVRGYRGYPDCQPCNCSGLGSTNQDPCIGPCSCKENVEGEDCSHCKFGFFNLQEENQKGCEECFCSGVSDRCQSSYWTYGNIQDMHGWYLTDLSGRIQVAPQLDNPDAPQQISVSNSEARRSLPDSYYWSAPAPYLRNKLPAVGGQLSFTISYDLEEEEDDTEKILQLMIILEGNNLRISTAYKEVHLEPSEEHVEELSLKEESFTIHGTNLPVSRKDFMILLTNLERVLIQTTYNLGMDVIFRLSSVNLESAVPYPTDRSIASAVEVCQCPPGYSGSSCEKRHPTNASSNPIPANASKACWPRHRRVNGTIFGGLCEPCQCFGHAEACNDVTGECLSCKDHTGGPYCNECLPGFYGDPTRGTSEDCQPCACPLNIPSNNFSPTCHLDRSLGLICDECPVGYTGPRCERCAEGYFGQPSIPGGSCQPCLCNDNLDFSIPGSCDSLSGSCLICKPGTTGRFCELCADGYFGDAVDAKNCQPCRCNVNGSFSEICHRKTGQCECRPNVQGQRCDECKPETFGLQLGRGCIPCNCNSFGSKSFDCEASGQCWCQPGVAGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCNPKTGQCICPPNTIGEKCSECLPNTWGHSIVTGCKVCNCSTVGSLSSQCNINTGQCSCHPKFSGMKCSECNRGHWNYPLCSLCDCFLPGTDATTCDSETRKCSCSDQTGQCTCKVNVEGVHCDRCRPGKFGLEAKNPLGCSSCYCFGVTSQCSEAKGLVRTWVTLRDEQTILPLVDEALQHTTTKGIAFQNPEIVAKMDEVRQDLHLEPFYWKLPEQFEGKKLMAYGGKLKYTIYFEARDETGFATYKPQVIIRGGTPTHARIITRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRISRTVTREDFLDILYDIHYILIKATYGNVVRQSRISEISMEGAEPGQVSAASPLANLIERCDCPPGYSGLSCETCAPGFYRVHSEPGGRTPGPTLGTCVPCQCHGHSSQCDPETSVCQNCQHHTAGDFCERCALGYYGIVRGLPNDCQPCACPLISPSNNFSPSCVLEGLEDYRCTACPRGYEGQYCERCAPGYAGSPSSPGGSCQECECDPYGSLPVPCDPVTGLCTCRPGATGRKCDGCEHGHAREGAECVFCGDECTGLLLGDLAHLEQMAMNINLTGPLPAPYKILYGLENATQELKHLLSPQRAPERLLQLAEGNMNTLVMEMNELLTRATKVTADGEQTGQDAERTNSRAQSLEEFIKGLVQHAEAVNEKAIKLNETLGSQDRTAERNLQELQKEIDRMLKELRSKDLQTQKEVAEDELVAAEGLLKRVNKLFGEPRAQNEEMEKDLREKLAEYQNKLDDAWDLLREATKKTKDADRLSAANQKNMTILETKKEAIEGSKRQIENTLKEGNDILDEANRLAGEITSVIDYVEDIKTKLPPMSEELSDKIDDLAQEIKDRRLAEKVFQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFRAYSNIKDYIDEAEKVAREAKELAHEATKLATSPQGLLKEDAKGSLQKSFRILNEAKKLANDVKENHNDLSGLKTRLETADLRNSGLLGALNDTMDKLSAIPNDTAAKLQAVKEKAREANDTAKAVLAQVKDLHQNLDGLKQNYNKLADSVAKTNAVVKDPSKNIADAGATVRNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIVVHVKTAVADNLLFYLGSAKFIDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIEASRTGRNGSISVRALDGPKASMVPSTHHSVSPPGYTILDVDANAMLFVGGLTGKIKKADAVRVTTFTGCMGETYFDNKPIGLWNFREKEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSNALLMYLATRDLKDFMSVELSDGHVKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDSNQEENIATSSSGNNFGLDLKADDKIYFGGLPTLRNLSMKARPEVNVKKYSGCLKDIEISRTPYNILSSPNYVGVTKGCSLENVYTVSFPKPGFVELAAVSIDVGTEINLSFSTRNESGIILLGSGGTLTPPRRKRRQTTQAYYAIFLNKGRLEVHLSSGTRTMRKIVIKPEPNLFHDGREHSVHVERTRGVFTVQVDENRRHMQNLTEEQPIEVKKLFVGGAPPEFQPSPLRNIPAFQGCVWNLVINSIPMDFAQPIAFKNADIGRCAYQKPREEEDDAVPAEVTVQPQPVPTPAFPFPAPTMVHGPCVAESEPAFLSGSKQFGLSRNSHIALAFDDTKVKNRLTIELEVRTEAESGLLFYMARINHADFATVQLRNGFPYFSYDLGSGDTSTMIPTRINDGQWHKIKITRVKQEGILSVDDASNQTISPKKADILDVVGILYVGGLPINYTTRRIGPVTYSLDGCVRNLYMEQAPVDLDQPTSSFHVGTCFANAEKGTYFDGTGFAKAVGGFKVGLDLLVEFEFRTTRPTGVLLGVSSQKMDGMGIEMIDEKLMFHVDNGAGRFTAVYDAGSPGHMCDGRWHKVTAKKIKNRLELVVDGNQVDAQSPNAASTSADTNDPVFVGGFPDGLNQFGLTTNVRFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPTT", "length": 3137, "header": "tr|A0A8I5ZPP7-1|A0A0G2JWX2_RAT Computationally mapped isoform of Laminin subunit alpha 2 OS=Rattus norvegicus OX=10116 GN=Lama2 PE=1 SV=1 CANONICAL=A0A0G2JWX2-1" }, "locus": { "chromosome": "1", "start_pos": 18320424, "end_pos": 17672766, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000102071.1", "url": "https://www.ensembl.org/id/ENSRNOT00000102071.1" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000078909.1", "url": "https://www.ensembl.org/id/ENSRNOP00000078909.1" } ] } }, { "isoform_ac": "F1M614-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JWX2/entry#F1M614-1", "sequence": { "sequence": "MPAAGGILLLLLLGILEGSQTQRPQQRRQSPAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSHPYQRHPITNAIDGKNTWWQSPSIKNGVEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDEEYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPATNKSRCECEHNTCGESCDRCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDETVASRNLSLNIHGKYIGGGVCINCTHNTAGINCETCIDGFFRPKGVSPSYPRPCQPCHCDPAGSLSEVCIKDEKHTRRGLKPGSCYCKPGFGGMNCDRCVRGYRGYPDCQPCNCSGLGSTNQDPCIGPCSCKENVEGEDCSHCKFGFFNLQEENQKGCEECFCSGVSDRCQSSYWTYGNIQDMHGWYLTDLSGRIQVAPQLDNPDAPQQISVSNSEARRSLPDSYYWSAPAPYLRNKLPAVGGQLSFTISYDLEEEEDDTEKILQLMIILEGNNLRISTAYKEVHLEPSEEHVEELSLKEESFTIHGTNLPVSRKDFMILLTNLERVLIQTTYNLGMDVIFRLSSVNLESAVPYPTDRSIASAVEVCQCPPGYSGSSCEACWPRHRRVNGTIFGGLCEPCQCFGHAEACNDVTGECLSCKDHTGGPYCNECLPGFYGDPTRGTSEDCQPCACPLNIPSNNFSPTCHLDRSLGLICDECPVGYTGPRCERCAEGYFGQPSIPGGSCQPCLCNDNLDFSIPGSCDSLSGSCLICKPGTTGRFCELCADGYFGDAVDAKNCQPCRCNVNGSFSEICHRKTGQCECRPNVQGQRCDECKPETFGLQLGRGCIPCNCNSFGSKSFDCEASGQCWCQPGVAGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCNPKTGQCICPPNTIGEKCSECLPNTWGHSIVTGCKVCNCSTVGSLSSQCNINTGQCSCHPKFSGMKCSECNRGHWNYPLCSLCDCFLPGTDATTCDSETRKCSCSDQTGQCTCKVNVEGVHCDRCRPGKFGLEAKNPLGCSSCYCFGVTSQCSEAKGLVRTWVTLRDEQTILPLVDEALQHTTTKGIAFQNPEIVAKMDEVRQDLHLEPFYWKLPEQFEGKKLMAYGGKLKYTIYFEARDETGFATYKPQVIIRGGTPTHARIITRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRISRTVTREDFLDILYDIHYILIKATYGNVVRQSRISEISMEGAEPGQVSAASPLANLIERCDCPPGYSGLSCETCAPGFYRVHSEPGGRTPGPTLGTCVPCQCHGHSSQCDPETSVCQNCQHHTAGDFCERCALGYYGIVRGLPNDCQPCACPLISPSNNFSPSCVLEGLEDYRCTACPRGYEGQYCERCAPGYAGSPSSPGGSCQECECDPYGSLPVPCDPVTGLCTCRPGATGRKCDGCEHGHAREGAECVFCGDECTGLLLGDLAHLEQMAMNINLTGPLPAPYKILYGLENATQELKHLLSPQRAPERLLQLAEGNMNTLVMEMNELLTRATKVTADGEQTGQDAERTNSRAQSLEEFIKGLVQHAEAVNEKAIKLNETLGSQDRTAERNLQELQKEIDRMLKELRSKDLQTQKEVAEDELVAAEGLLKRVNKLFGEPRAQNEEMEKDLREKLAEYQNKLDDAWDLLREATKKTKDADRLSAANQKNMTILETKKEAIEGSKRQIENTLKEGNDILDEANRLAGEITSVIDYVEDIKTKLPPMSEELSDKIDDLAQEIKDRRLAEKVFQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFRAYSNIKDYIDEAEKVAREAKELAHEATKLATSPQGLLKEDAKGSLQKSFRILNEAKKLANDVKENHNDLSGLKTRLETADLRNSGLLGALNDTMDKLSAIPNDTAAKLQAVKEKAREANDTAKAVLAQVKDLHQNLDGLKQNYNKLADSVAKTNAVVKDPSKNSKIADAGATVRNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIVVHVKTAVADNLLFYLGSAKFIDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIEASRTGRNGSISVRALDGPKASMVPSTHHSVSPPGYTILDVDANAMLFVGGLTGKIKKADAVRVTTFTGCMGETYFDNKPIGLWNFREKEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSNALLMYLATRDLKDFMSVELSDGHVKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDSNQEENIATSSSGNNFGLDLKADDKIYFGGLPTLRNLRPEVNVKKYSGCLKDIEISRTPYNILSSPNYVGVTKGCSLENVYTVSFPKPGFVELAAVSIDVGTEINLSFSTRNESGIILLGSGGTLTPPRRKRRQTTQAYYAIFLNKGRLEVHLSSGTRTMRKIVIKPEPNLFHDGREHSVHVERTRGVFTVQVDENRRHMQNLTEEQPIEVKKLFVGGAPPEFQPSPLRNIPAFQGCVWNLVINSIPMDFAQPIAFKNADIGRCAYQKPREEEDDAVPAEVTVQPQPVPTPAFPFPAPTMVHGPCVAESEPAFLSGSKQFGLSRNSHIALAFDDTKVKNRLTIELEVRTEAESGLLFYMARINHADFATVQLRNGFPYFSYDLGSGDTSTMIPTRINDGQWHKIKITRVKQEGILSVDDASNQTISPKKADILDVVGILYVGGLPINYTTRRIGPVTYSLDGCVRNLYMEQAPVDLDQPTSSFHVGTCFANAEKGTYFDGTGFAKAVGGFKVGLDLLVEFEFRTTRPTGVLLGVSSQKMDGMGIEMIDEKLMFHVDNGAGRFTAVYDAGSPGHMCDGRWHKVTAKKIKNRLELVVDGNQVDAQSPNAASTSADTNDPVFVGGFPDGLNQFGLTTNVRFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPTT", "length": 3117, "header": "tr|F1M614-1|A0A0G2JWX2_RAT Computationally mapped isoform of Laminin subunit alpha 2 OS=Rattus norvegicus OX=10116 GN=Lama2 PE=1 SV=4 CANONICAL=A0A0G2JWX2-1" }, "locus": { "chromosome": "1", "start_pos": 18320424, "end_pos": 17672766, "strand": "-", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000014917.8", "url": "https://www.ensembl.org/id/ENSRNOT00000014917.8" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000014917.8", "url": "https://www.ensembl.org/id/ENSRNOP00000014917.8" } ] } } ], "glycosylation": [ { "glytoucan_ac": "", "type": "O-linked", "subtype": "other", "prediction_tool": "isoglyp", "mining_tool": "", "site_category": "predicted", "site_category_dict": { "predicted": true }, "site_seq": "", "relation": "attached", "comment": "", "start_pos": 1412, "start_aa": "T", "end_pos": 1412, "end_aa": "T", "residue": "Thr", "site_lbl": "Thr1412", "evidence": [ { "id": "GLY_001157", "database": "GlyGen", "url": "https://data.glygen.org/GLY_001157" } ], "filter_code": "00000000000000001000.00000000001000.1.01000" }, { "glytoucan_ac": "", "type": "O-linked", "subtype": "other", "prediction_tool": "isoglyp", "mining_tool": "", "site_category": "predicted", "site_category_dict": { "predicted": true }, "site_seq": "", "relation": "attached", "comment": "", "start_pos": 2735, "start_aa": "T", "end_pos": 2735, "end_aa": "T", "residue": "Thr", "site_lbl": "Thr2735", "evidence": [ { "id": "GLY_001157", "database": "GlyGen", "url": "https://data.glygen.org/GLY_001157" } ], "filter_code": "00000000000000001000.00000000001000.1.01000" } ], "phosphorylation": [], "glycation": [], "keywords": [ "glycoprotein", "glycoprotein_predicted" ], "publication": [], "pathway": [], "orthologs": [ { "uniprot_canonical_ac": "A0A287A027-1", "protein_name": "Laminin subunit alpha 2", "gene_name": "LAMA2", "tax_id": 9823, "organism": "Sus scrofa", "sequence": { "sequence": "MPGAARVLLVLLLSGGFGGGRTQRPQQQQELRRQPPAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSNPYQRHPITNAIDGKNTWWQSPSIKNGIEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDVDYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSIKDISVGGMCICYGHARACPLDPVTNKSRCECEHNTCGDSCDQCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDENVARRNLSLNIRGKYIGGGVCINCTRNTDGINCETCIDGFFRPKGVSPNHPRPCQPCHCDPVGSLNEVCVKDEKRARRGLAPGSCHCKPGFKGVSCDRCARGYTGYPDCRPCNCSGAGSTNEDPCFGPCKCKENVEGGDCSRCKSGFFNLQEDNHKGCDECFCSGVSNRCQSSYWTYGNIQDMSGWYLTDISGHIQVAPQQDDMDPPRQISISSSEARRALPQSYFWSAPAPYLGNKLTAAGGELTFTVSYDLEEEEDDDTERILQLMIILEGNNLRISTAQDEVYLKPSKEHINVLTLKEELFTIHGTNFPVSRKEFMTVLANLKRVLIQITYSLGMDAIFRLSSVGLESAGPYPTDRSFAAAVEVCQCPPGYTGSSCERRHPANASSNLIPANNAKACWPRHRRVNGTIFGGICEPCQCFGHAESCDDITGECLNCKDHTGGPYCNKCLPGFYGDPTKGTSDDCQPCACPLNIPSNNFSPTCHLDRSLGLICDKCPVGYIGPRCERCAEGYFGQPSVPGGSCQPCQCNDNLDFSIPGSCDSLSGSCLICKPGTTGRYCELCADGYFGDAVDAKNCQPCHCNANGSFSDVCHTRTGQCECKPNVQGRRCDECKPAMWWDPEKRLCVSCGCNPVGSMTPQCDISGRCVCKSSFVGKRCNLSRQVHRQEKQPQRAQRVLGSPQRWGVSSSSGCPRGAYRPLAPPETFGLQSARGCIPCNCNSFGSKSFDCEESGQCWCQPGVTGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCDPKTGQCICPPNTIGEKCSKCAPNTWGHSIITGCKACNCSSIGSLDFQCNVNTGQCNCRPKFSGAKCTECNRGHWNYPHCSPCDCFLPGTDDSSCDLETKKCSCIDQTGQCTCKVNVEGVHCDRCRPGKFGLDAKNPLGCSSCYCFGVTTQCSEAKGLIRTWVTLQPEQTILPLVDEALQHTTTKGIAFQHPEIIAHMELVRQDLHLEPFYWKLPEQFEGKKLMAYGGKLKYAIYFEAREETGFSTYNPQVIIRGGTPTHARIIIRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRVSRTVTREDFLDILYDIHYILIKATYGNIMRQSRISEISMEVAEQGRITAVTPPAHLIERCDCPPGYSGLSCEACMPGFYRLRSKPGGLTPGPTLGTCVPCQCHGHSSLCDPETSICQNCQHHTAGDFCEQCAPGYYGIVKGLPDDCQQCACPLISSSNNFSPSCVLEGLDDHRCTACPRGYEGQYCERCAPGYAGSPSSPGGSCQECECDPHGSLPVPCDPVTGICRCRPGATGPKCDGCKHWHAREGMECVFCGDECTGLLLGDLARLEQMAMSINLTGPLPAPYKILYGLENMTQELKHLLSPQRAPERLIQLAEGNLNTLVTEMNELLTRATKVTADGEQTGQDAERTNTRANSLGEFIKDLARDAEAVNEKAVKLNETLGTQEKAFERNLQDLQNEIDQMMTALRRRNLDTQKEVAEDELVAAEGLLKKVKKLFGESRGKNEAMEKDLQEKLADYQNKVDDAWDLLREATDKIREANLLSAENQKNMTALEKKKEAIESGKRQTENTLKEGNDILEEANRLADEINSVIDYVQDIQTKLPTMSEDLQDKIDDLSQEIKDRKLAEKVSQAESHAAQLNDSSAVLDGILEEAKNISFNATAAFKAYSNIKDYIDEAEKIAKEAKVLAHEATELVRNK", "length": 2070 }, "evidence": [ { "id": "A0A0G2JWX2", "url": "https://omabrowser.org/oma/group/A0A0G2JWX2/", "database": "OMA" } ], "glygen_name": "Pig", "common_name": "Pig" }, { "uniprot_canonical_ac": "A0A3Q1MFB8-1", "protein_name": "Laminin subunit alpha 2", "gene_name": "LAMA2", "tax_id": 9913, "organism": "Bos taurus", "sequence": { "sequence": "MPRAFGVLLVLLLSGGLGGGQAQRPERQQQQQHRWQPPAHQQRGLFPAVLNLASSALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSNPYQRHPITNAIDGKNTWWQSPSIKNGIEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDNVVYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPVTNKSRCECEHNTCGDSCDQCCPGFHQKPWRAGTFLTKSECEACNCHGKAEECYYDENVARRNRSLNIHGKYIGGGVCINCTRNTAGINCETCIDGFFRPKGVSPNYPRPCQPCHCDPVGSLNEVCVKDEKHARRGLAPGSCHCKPGFRGVSCDRCARGYIGYPDCKPCNCSGAGSTNEDPCFGPCNCKENVEGGDCSRCKFGFFNLQEDNHKGCDECFCSGVSNRCQSSYWTYGNIQDMSGWYLTDISGHIRVAPQLDDLDPPQQISISSVEARQALPQSYFWSAPAPYLGNKLTAAGGQLMFTVSYDLEEANEDAEHTLQLMVILEGKDLRISSAQEEVYLQPSEEHINVLSLKEESFTTHGTNFPVSRKEFMTVLVNLQRILIQITYSLGMDAIFRLSSVNLESAVPISPDGSFATAVEVCQCPPGYTGSSCESCWPRHRRVNGTIFGGLCEPCQCFGHAESCDDTTGECLNCKDHTDGPYCDKCLPGFYGDPTKGTSDDCQPCACPLNSPSNNFSPTCHMDRSLGLICDECPVGYSGQRCERCAEGYFGQPSVPGGSCQPCQCNDNLDFSIPGSCDSLSGSCLICKPGTTGRYCELCADGYFGDAVDAKNCQPCHCNANGSFSEVCHAQTGQCECKPNVQGRRCDECKPETFGLQSARGCIPCNCNSFGSKSFDCEESGQCWCQPGVTGKKCDRCAHGYFNFQEGGCTACDCSHLGNNCDPKTGRCICPPNTIGEKCSKCAPRTWGHSITTGCKACNCSSVGSLDFQCDLNMGQCKCHPKFSGAKCTECTRGHWNYPHCSPCDCFLSGTDDSTCDLETKKCSCIDQTGQCTCKVNVEGIHCDRCRPGKFGLEAKNPLGCNSCYCFGATTQCSEAKGLIRTWVTLKPEQTILPLVDEALQHTTTKGIIFQHPEIVAHMDLVRQELHLEPFYWKLPEQFEGKKLMAYGGKLRYTIYFEAREETGFSTYNPQVIIRGGTPAHARIIIRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRISRTVTREDFLDVLYDIHYILIKATYGNIMRQSRISEISMEVAEPGRITAVTPPAHLIEKCDCPPGYSGLSCETCTPGFYRLRSEPGGRTPGATLGTCVPCQCHGHSNLCDPETSICQNCQHHTAGDFCERCALGYYGIVKGLPNDCQQCACPLISSSNNFSPSCIMEGLDDYRCTACPRGYEGKYCERCAPGYAGSPSSPGGSCQECECDPHGSLPVPCDPVMGICTCRPGATGPKCDGCEQGHAREGMECVFCGDECTGLLLGDLARLEQMATSINLTGPLPAPYKILYGLENMTQELKNLLSPQRAPERLIQLAEGNLNMLVTEMNELLTRATKVTADGEQTGQDAERTNVRADSVGAFIKALAQDAEAVNEKAVKLNETLGTKDKAFERNLQELQNEIDQMMTELRRKNLDTQKEVAEDELVAAEGLLKKVKKLFGESRGKNEEMEKDLREKLADYESKVDDAWDLLREATDKIREANLLSAENQKNMTALEKKKEAIESGKRQTENTLKEGNDILDEASRLVDEINSVIVYVEDIQTKLPPMSKDLKDKIDDLSQKIKDRKLAEKVSQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFNAYSNIKDYIDEAEKIAKEAKVLAHEATELAAGPQGSLKEGAKGSLQKSFGILNEAKKLANDVKENDDRLNGLTARLDDANIRNGDLLRALNDTLDKLAAIPNDTAAKLQAVKDKARQANDTAKDVLAQIKDLHQNLDGLKKNYNQLADSVAKTNAVVKDPSKNIADADATVKNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIIVNVKTAVADNLLFYLGSAKFVDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIEASRTGRNGTISVRALDGPKASIMPSTYHSASPPGYTILDVDANAMLFVGGLTGKLKKADAVRVITFTGCMGEAYFDSKPIGLWNFREIEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSSALLMYLATRDLKDFMSVELTDGHIKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDTNQEENIATSSPGNNFGLDLKADDKIYFGGLPTLRNLSMKARPEVNVKKYSGCLKDIEISRTPYNILSSPDYVGVTKGCSLENVYTVSFPKPGFVELSPVPIDVGTEINLSFSTKNESGIILLGSGGTPIPPRRKRRQTGQVYYAIFLNKGRLEVHLSTGARTMRKIVVKPEPSLFHDGREHSVHVERTRGMFTVQVDEDRKHMQNLTMEQAIEVKKLFIGGAPPEFQPSPLRNIPPFEGCIWNLVINSVPMDFAQPVSFKNADIGRCAHQKPPEEEDGAVTAETVTQPELVPTPVVPAPTPFLTHGPCAAESEPALLIGSKQFGLSRNSHIAIAFDDTKVKNRLTIEFEVRTEAESGLLFYMARINHADFATVQLKNGLPYFSYDLGSGDTSTMIPTKINDGQWHKIKILRVKQEGTIYVDDASNRTISPKKADILDVVGMLYVGGLPINYTTRRIGPVTYSIDGCIRNLHMVEAPADLEQPTSSYQVGTCFANAQKGTYFDGTGFAKAVDGFKVGLDLLVEFEFRTTRTTGVLLGISSQKMDGMGIEMIDEKLMFHVDNGAGRFTAIYDAGVPGHLCDGQWHKVTANKIKHRIELTVDGNQVEAQSPNRASTSADTNDPVFVGGFPDGLNQFGLTTNIPFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPAN", "length": 3126 }, "evidence": [ { "id": "A0A0G2JWX2", "url": "https://omabrowser.org/oma/group/A0A0G2JWX2/", "database": "OMA" } ], "glygen_name": "Bovine", "common_name": "Bovine" }, { "uniprot_canonical_ac": "P24043-1", "protein_name": "Laminin subunit alpha-2", "gene_name": "LAMA2", "tax_id": 9606, "organism": "Homo sapiens", "sequence": { "sequence": "MPGAAGVLLLLLLSGGLGGVQAQRPQQQRQSQAHQQRGLFPAVLNLASNALITTNATCGEKGPEMYCKLVEHVPGQPVRNPQCRICNQNSSNPNQRHPITNAIDGKNTWWQSPSIKNGIEYHYVTITLDLQQVFQIAYVIVKAANSPRPGNWILERSLDDVEYKPWQYHAVTDTECLTLYNIYPRTGPPSYAKDDEVICTSFYSKIHPLENGEIHISLINGRPSADDPSPELLEFTSARYIRLRFQRIRTLNADLMMFAHKDPREIDPIVTRRYYYSVKDISVGGMCICYGHARACPLDPATNKSRCECEHNTCGDSCDQCCPGFHQKPWRAGTFLTKTECEACNCHGKAEECYYDENVARRNLSLNIRGKYIGGGVCINCTQNTAGINCETCTDGFFRPKGVSPNYPRPCQPCHCDPIGSLNEVCVKDEKHARRGLAPGSCHCKTGFGGVSCDRCARGYTGYPDCKACNCSGLGSKNEDPCFGPCICKENVEGGDCSRCKSGFFNLQEDNWKGCDECFCSGVSNRCQSSYWTYGKIQDMSGWYLTDLPGRIRVAPQQDDLDSPQQISISNAEARQALPHSYYWSAPAPYLGNKLPAVGGQLTFTISYDLEEEEEDTERVLQLMIILEGNDLSISTAQDEVYLHPSEEHTNVLLLKEESFTIHGTHFPVRRKEFMTVLANLKRVLLQITYSFGMDAIFRLSSVNLESAVSYPTDGSIAAAVEVCQCPPGYTGSSCESCWPRHRRVNGTIFGGICEPCQCFGHAESCDDVTGECLNCKDHTGGPYCDKCLPGFYGEPTKGTSEDCQPCACPLNIPSNNFSPTCHLDRSLGLICDGCPVGYTGPRCERCAEGYFGQPSVPGGSCQPCQCNDNLDFSIPGSCDSLSGSCLICKPGTTGRYCELCADGYFGDAVDAKNCQPCRCNAGGSFSEVCHSQTGQCECRANVQGQRCDKCKAGTFGLQSARGCVPCNCNSFGSKSFDCEESGQCWCQPGVTGKKCDRCAHGYFNFQEGGCTACECSHLGNNCDPKTGRCICPPNTIGEKCSKCAPNTWGHSITTGCKACNCSTVGSLDFQCNVNTGQCNCHPKFSGAKCTECSRGHWNYPRCNLCDCFLPGTDATTCDSETKKCSCSDQTGQCTCKVNVEGIHCDRCRPGKFGLDAKNPLGCSSCYCFGTTTQCSEAKGLIRTWVTLKAEQTILPLVDEALQHTTTKGIVFQHPEIVAHMDLMREDLHLEPFYWKLPEQFEGKKLMAYGGKLKYAIYFEAREETGFSTYNPQVIIRGGTPTHARIIVRHMAAPLIGQLTRHEIEMTEKEWKYYGDDPRVHRTVTREDFLDILYDIHYILIKATYGNFMRQSRISEISMEVAEQGRGTTMTPPADLIEKCDCPLGYSGLSCEACLPGFYRLRSQPGGRTPGPTLGTCVPCQCNGHSSLCDPETSICQNCQHHTAGDFCERCALGYYGIVKGLPNDCQQCACPLISSSNNFSPSCVAEGLDDYRCTACPRGYEGQYCERCAPGYTGSPGNPGGSCQECECDPYGSLPVPCDPVTGFCTCRPGATGRKCDGCKHWHAREGWECVFCGDECTGLLLGDLARLEQMVMSINLTGPLPAPYKMLYGLENMTQELKHLLSPQRAPERLIQLAEGNLNTLVTEMNELLTRATKVTADGEQTGQDAERTNTRAKSLGEFIKELARDAEAVNEKAIKLNETLGTRDEAFERNLEGLQKEIDQMIKELRRKNLETQKEIAEDELVAAEALLKKVKKLFGESRGENEEMEKDLREKLADYKNKVDDAWDLLREATDKIREANRLFAVNQKNMTALEKKKEAVESGKRQIENTLKEGNDILDEANRLADEINSIIDYVEDIQTKLPPMSEELNDKIDDLSQEIKDRKLAEKVSQAESHAAQLNDSSAVLDGILDEAKNISFNATAAFKAYSNIKDYIDEAEKVAKEAKDLAHEATKLATGPRGLLKEDAKGCLQKSFRILNEAKKLANDVKENEDHLNGLKTRIENADARNGDLLRTLNDTLGKLSAIPNDTAAKLQAVKDKARQANDTAKDVLAQITELHQNLDGLKKNYNKLADSVAKTNAVVKDPSKNKIIADADATVKNLEQEADRLIDKLKPIKELEDNLKKNISEIKELINQARKQANSIKVSVSSGGDCIRTYKPEIKKGSYNNIVVNVKTAVADNLLFYLGSAKFIDFLAIEMRKGKVSFLWDVGSGVGRVEYPDLTIDDSYWYRIVASRTGRNGTISVRALDGPKASIVPSTHHSTSPPGYTILDVDANAMLFVGGLTGKLKKADAVRVITFTGCMGETYFDNKPIGLWNFREKEGDCKGCTVSPQVEDSEGTIQFDGEGYALVSRPIRWYPNISTVMFKFRTFSSSALLMYLATRDLRDFMSVELTDGHIKVSYDLGSGMASVVSNQNHNDGKWKSFTLSRIQKQANISIVDIDTNQEENIATSSSGNNFGLDLKADDKIYFGGLPTLRNLSMKARPEVNLKKYSGCLKDIEISRTPYNILSSPDYVGVTKGCSLENVYTVSFPKPGFVELSPVPIDVGTEINLSFSTKNESGIILLGSGGTPAPPRRKRRQTGQAYYAILLNRGRLEVHLSTGARTMRKIVIRPEPNLFHDGREHSVHVERTRGIFTVQVDENRRYMQNLTVEQPIEVKKLFVGGAPPEFQPSPLRNIPPFEGCIWNLVINSVPMDFARPVSFKNADIGRCAHQKLREDEDGAAPAEIVIQPEPVPTPAFPTPTPVLTHGPCAAESEPALLIGSKQFGLSRNSHIAIAFDDTKVKNRLTIELEVRTEAESGLLFYMARINHADFATVQLRNGLPYFSYDLGSGDTHTMIPTKINDGQWHKIKIMRSKQEGILYVDGASNRTISPKKADILDVVGMLYVGGLPINYTTRRIGPVTYSIDGCVRNLHMAEAPADLEQPTSSFHVGTCFANAQRGTYFDGTGFAKAVGGFKVGLDLLVEFEFRTTTTTGVLLGISSQKMDGMGIEMIDEKLMFHVDNGAGRFTAVYDAGVPGHLCDGQWHKVTANKIKHRIELTVDGNQVEAQSPNPASTSADTNDPVFVGGFPDDLKQFGLTTSIPFRGCIRSLKLTKGTGKPLEVNFAKALELRGVQPVSCPAN", "length": 3122 }, "evidence": [ { "id": "A0A0G2JWX2", "url": "https://omabrowser.org/oma/group/A0A0G2JWX2/", "database": "OMA" } ], "glygen_name": "Human", "common_name": "Human" }, { "uniprot_canonical_ac": "Q60675-1", "protein_name": "Laminin subunit alpha-2", "gene_name": "Lama2", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": 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"https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "animal organ morphogenesis", "id": "GO:0009887", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009887", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "regulation of cell migration", "id": "GO:0030334", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030334", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "Schwann cell differentiation", "id": "GO:0014037", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0014037", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "axon guidance", "id": "GO:0007411", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007411", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "tissue development", "id": "GO:0009888", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009888", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "regulation of embryonic development", "id": "GO:0045995", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045995", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" } ] }, { "name": "Molecular Function", "total": 2, "go_terms": [ { "name": "signaling receptor binding", "id": "GO:0005102", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005102", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "extracellular matrix structural constituent", "id": "GO:0005201", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005201", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" } ] }, { "name": "Cellular Component", "total": 5, "go_terms": [ { "name": "neuromuscular junction", "id": "GO:0031594", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031594", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "dendritic spine", "id": "GO:0043197", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043197", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "synaptic cleft", "id": "GO:0043083", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0043083", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JWX2", "url": "https://www.uniprot.org/uniprot/A0A0G2JWX2" } ], "pmid": "" }, { "name": "sarcolemma", "id": 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