{
    "uniprot_canonical_ac": "A6H5Y3-1", 
    "ptm_annotation": [], 
    "sequence": {
        "header": "sp|A6H5Y3-1|METH_MOUSE Isoform 1 of Methionine synthase  OS=Mus musculus OX=10090 GN=Mtr PE=1 SV=1 CANONICAL=A6H5Y3-1", 
        "length": 1253, 
        "sequence": "MKKTLQDEIEAILRKRIMVLDGGMGTMIQRYKLSEEHFQGQEFKDHSRPLKGNNDILSITQPDIIYQIHKEYLLAGADIIETNTFSSTSIAQADYGLEHLAYRMNKCSADVARKAAEEITLQTGVKRFVAGALGPTNKTLSVSPSVERPDYRNITFDELVDAYQEQAKGLLDGRVDILLIETIFDTANAKAALFAIQNLFEENYAPPRPIFISGTIVDKSGRTLSGQTGEAFVTSVSHSDPLCIGLNCSLGAAEMRPFIETIGKCTTAYVLCYPNAGLPNTFGDYDETPSTMATHLKDFAVDGLVNIVGGCCGSTPDHIREIAEAVKKCKPRVPPASVFEGHMLLSGLEPFRIGPYTNFVNIGERCNVAGSRKFAKLIMAGNYEEALSIAKAQVEMGAQVLDINMDDGMLDGPSAMTRFCNSIASEPDIAKVPLCIDSSNFAVIEAGLKCCQGKCIVNSISLKEGEGDFLEKARKIKKFGAAVVVMAFDEEGQATETDVKVNVCTRAYHLLVDKVGFNPNDIIFDPNILTIGTGMEEHNLYAINFIHATRVIKETLPGVRISGGLSNLSFSFRGMEAIREAMHGVFLYHAIKFGMDMGIVNAGNLPVYDAIHKDLLQLCEDLIWNKDSEATEKLLRYAQTHGTGGKKVIQTDEWRNGSIEERLEYALVKGIEKHIVEDTEEARLNGEKYPRPLNIIEGPLMNGMKVVGDLFGAGKMFLPQVIKSARVMKKAVGHLIPFMEKEREEARLINGSVEEEDPYQGTIVLATVKGDVHDIGKNIVGVVLACNNFRVIDLGVMTPCDKILQAALDHKADIIGLSGLITPSLDEMIFVAKEMERLAIKIPLLIGGATTSRTHTAVKIAPRYSAPVIHVLDASKSVVVCSQLLDENLRDDYFEEILEEYEDIRQDHYESLKERKYVPLSQARKHGFHIDWLSEPHPVKPTFIGTQVFEDYNLQKLVDYIDWKPFFDVWQLRGKYPNRGFPKIFNDKAVGEEARKVYNDAQNMLNILISQKKLQARGVVGFWPAQSVQDDIHLYAEGVVPQAAEPIATFYGLRQQAEKDSSSTDPYHCLSDFIAPLHSGVCDYLGLFAVACFGVEELSKTYEDDGDDYSSIMVKALGDRLAEAFAEELHERVRRELWAYSRSEQLGVPDLRRLRYEGIRPAPGYPSQPDHTEKLTMWRLASIEQATGIRLTESLAMAPASAVSGLYFSNVKAKYFAVGKISKDQTEDYALRKNMPVAEVEKWLGPILGYDTD"
    }, 
    "uniprot_id": "METH_MOUSE", 
    "enzyme_annotation": [
        {
            "ec": "2.1.1.13", 
            "activity": ""
        }, 
        {
            "ec": "2.1.1.13", 
            "activity": "5-methyltetrahydrofolate + L-homocysteine = tetrahydrofolate + L-methionine."
        }
    ], 
    "glycation": [], 
    "keywords": [], 
    "species": [
        {
            "common_name": "Mouse", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                    "id": "A6H5Y3", 
                    "database": "UniProtKB"
                }
            ], 
            "name": "Mus musculus", 
            "taxid": 10090
        }
    ], 
    "publication": [
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/11110696", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "11110696"
                }
            ], 
            "title": "Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.", 
            "journal": "Blood", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Gwynn B, Ciciotte SL, Hunter SJ, Washburn LL, Smith RS, Andersen SG, Swank RT, Dell'Angelica EC, Bonifacino JS, Eicher EM, Peters LL", 
            "date": "2000"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/11440986", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "11440986"
                }
            ], 
            "title": "Differential expression of the actin-binding proteins, alpha-actinin-2 and -3, in different species: implications for the evolution of functional redundancy.", 
            "journal": "Human molecular genetics", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Mills M, Yang N, Weinberger R, Vander Woude DL, Beggs AH, Easteal S, North K", 
            "date": "2001"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/12520002", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "12520002"
                }
            ], 
            "title": "BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.", 
            "journal": "Nucleic acids research", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Stryke D, Kawamoto M, Huang CC, Johns SJ, King LA, Harper CA, Meng EC, Lee RE, Yee A, L'Italien L, Chuang PT, Young SG, Skarnes WC, Babbitt PC, Ferrin TE", 
            "date": "2003"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/17937387", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "17937387"
                }
            ], 
            "title": "Glycine N-methyltransferase-/- mice develop chronic hepatitis and glycogen storage disease in the liver.", 
            "journal": "Hepatology (Baltimore, Md.)", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Liu SP, Li YS, Chen YJ, Chiang EP, Li AF, Lee YH, Tsai TF, Hsiao M, Huang SF, Chen YM", 
            "date": "2007"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/19158324", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "19158324"
                }
            ], 
            "title": "Regulation of homocysteine homeostasis through the transcriptional coactivator PGC-1alpha.", 
            "journal": "American journal of physiology. Endocrinology and metabolism", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Li S, Arning E, Liu C, Vitvitsky V, Hernandez C, Banerjee R, Bottiglieri T, Lin JD", 
            "date": "2009"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/22365888", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "22365888"
                }
            ], 
            "title": "Spatial and temporal expression of folate-related transporters and metabolic enzymes during mouse placental development.", 
            "journal": "Placenta", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Cherukad J, Wainwright V, Watson ED", 
            "date": "2012"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/30753104", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "30753104"
                }
            ], 
            "title": "Betaine-homocysteine S-methyltransferase deficiency causes increased susceptibility to noise-induced hearing loss associated with plasma hyperhomocysteinemia.", 
            "journal": "FASEB journal : official publication of the Federation of American Societies for Experimental Biology", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Partearroyo T, Murillo-Cuesta S, Vallecillo N, Bermudez-Munoz JM, Rodriguez-de la Rosa L, Mandruzzato G, Celaya AM, Zeisel SH, Pajares MA, Varela-Moreiras G, Varela-Nieto I", 
            "date": "2019"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/9321480", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "9321480"
                }
            ], 
            "title": "The methionine synthase (Mtr) gene maps to proximal mouse chromosome 13.", 
            "journal": "Mammalian genome : official journal of the International Mammalian Genome Society", 
            "evidence": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
                    "id": "NP_001074597.1", 
                    "database": "RefSeq"
                }
            ], 
            "authors": "Zhang ZX, Leclerc D, Gravel R, Rozen R", 
            "date": "1997"
        }
    ], 
    "uniprot_ac": "A6H5Y3", 
    "site_annotation": [
        {
            "end_pos": 139, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 137
        }, 
        {
            "end_pos": 155, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 153
        }, 
        {
            "end_pos": 249, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 247
        }, 
        {
            "end_pos": 569, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 567
        }, 
        {
            "end_pos": 658, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 656
        }, 
        {
            "end_pos": 752, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 750
        }
    ], 
    "isoforms": [
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#A0A1Y7VM88-1", 
            "isoform_ac": "A0A1Y7VM88-1", 
            "locus": {
                "end_pos": 12241658, 
                "strand": "+", 
                "start_pos": 12253973, 
                "chromosome": "13", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000221290", 
                        "id": "ENSMUST00000221290", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000152579", 
                        "id": "ENSMUSP00000152579", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A1Y7VM88-1|METH_MOUSE Computationally mapped isoform of Methionine synthase  OS=Mus musculus OX=10090 GN=Mtr PE=1 SV=1 CANONICAL=A6H5Y3-1", 
                "length": 222, 
                "sequence": "MKKTLQDEIEAILRKRIMVLDGGMGTMIQRYKLSEEHFQGQEFKDHSRPLKGNNDILSITQPDIIYQIHKEYLLAGADIIETNTFSSTSIAQADYGLEHLESRGLWLELWVRLIRHFLSPHLWKGQIIGTSHLMSLLTHTRSRPRDCWMAGSTSYSLKQFLIQLMPKQPCLRSRTSLKRIMLLLGLSLFLGPLLIKVEGLFLGRRERLLSPACLIRTPCALD"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#A6H5Y3-1", 
            "isoform_ac": "A6H5Y3-1", 
            "locus": {
                "end_pos": 12187008, 
                "strand": "+", 
                "start_pos": 12253973, 
                "chromosome": "13", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000099856", 
                        "id": "ENSMUST00000099856", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000097442", 
                        "id": "ENSMUSP00000097442", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A6H5Y3-1|METH_MOUSE Isoform 1 of Methionine synthase  OS=Mus musculus OX=10090 GN=Mtr PE=1 SV=1 CANONICAL=A6H5Y3-1", 
                "length": 1253, 
                "sequence": "MKKTLQDEIEAILRKRIMVLDGGMGTMIQRYKLSEEHFQGQEFKDHSRPLKGNNDILSITQPDIIYQIHKEYLLAGADIIETNTFSSTSIAQADYGLEHLAYRMNKCSADVARKAAEEITLQTGVKRFVAGALGPTNKTLSVSPSVERPDYRNITFDELVDAYQEQAKGLLDGRVDILLIETIFDTANAKAALFAIQNLFEENYAPPRPIFISGTIVDKSGRTLSGQTGEAFVTSVSHSDPLCIGLNCSLGAAEMRPFIETIGKCTTAYVLCYPNAGLPNTFGDYDETPSTMATHLKDFAVDGLVNIVGGCCGSTPDHIREIAEAVKKCKPRVPPASVFEGHMLLSGLEPFRIGPYTNFVNIGERCNVAGSRKFAKLIMAGNYEEALSIAKAQVEMGAQVLDINMDDGMLDGPSAMTRFCNSIASEPDIAKVPLCIDSSNFAVIEAGLKCCQGKCIVNSISLKEGEGDFLEKARKIKKFGAAVVVMAFDEEGQATETDVKVNVCTRAYHLLVDKVGFNPNDIIFDPNILTIGTGMEEHNLYAINFIHATRVIKETLPGVRISGGLSNLSFSFRGMEAIREAMHGVFLYHAIKFGMDMGIVNAGNLPVYDAIHKDLLQLCEDLIWNKDSEATEKLLRYAQTHGTGGKKVIQTDEWRNGSIEERLEYALVKGIEKHIVEDTEEARLNGEKYPRPLNIIEGPLMNGMKVVGDLFGAGKMFLPQVIKSARVMKKAVGHLIPFMEKEREEARLINGSVEEEDPYQGTIVLATVKGDVHDIGKNIVGVVLACNNFRVIDLGVMTPCDKILQAALDHKADIIGLSGLITPSLDEMIFVAKEMERLAIKIPLLIGGATTSRTHTAVKIAPRYSAPVIHVLDASKSVVVCSQLLDENLRDDYFEEILEEYEDIRQDHYESLKERKYVPLSQARKHGFHIDWLSEPHPVKPTFIGTQVFEDYNLQKLVDYIDWKPFFDVWQLRGKYPNRGFPKIFNDKAVGEEARKVYNDAQNMLNILISQKKLQARGVVGFWPAQSVQDDIHLYAEGVVPQAAEPIATFYGLRQQAEKDSSSTDPYHCLSDFIAPLHSGVCDYLGLFAVACFGVEELSKTYEDDGDDYSSIMVKALGDRLAEAFAEELHERVRRELWAYSRSEQLGVPDLRRLRYEGIRPAPGYPSQPDHTEKLTMWRLASIEQATGIRLTESLAMAPASAVSGLYFSNVKAKYFAVGKISKDQTEDYALRKNMPVAEVEKWLGPILGYDTD"
            }
        }
    ], 
    "pathway": [
        {
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:238505", 
            "resource": "KEGG Pathway", 
            "id": "mmu:238505", 
            "name": ""
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-156581", 
            "resource": "Reactome", 
            "id": "R-MMU-156581", 
            "name": "Methylation"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-1614635", 
            "resource": "Reactome", 
            "id": "R-MMU-1614635", 
            "name": "Sulfur amino acid metabolism"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-196741", 
            "resource": "Reactome", 
            "id": "R-MMU-196741", 
            "name": "Cobalamin (Cbl, vitamin B12) transport and metabolism"
        }
    ], 
    "function": [
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#function", 
            "annotation": "Catalyzes the transfer of a methyl group from methylcob(III)alamin (MeCbl) to homocysteine, yielding enzyme-bound cob(I)alamin and methionine in the cytosol. MeCbl is an active form of cobalamin (vitamin B12) used as a cofactor for methionine biosynthesis. Cob(I)alamin form is regenerated to MeCbl by a transfer of a methyl group from 5-methyltetrahydrofolate. The processing of cobalamin in the cytosol occurs in a multiprotein complex composed of at least MMACHC, MMADHC, MTRR (methionine synthase reductase) and MTR which may contribute to shuttle safely and efficiently cobalamin towards MTR in order to produce methionine.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A6H5Y3#function", 
                    "id": "A6H5Y3", 
                    "database": "UniProtKB"
                }
            ]
        }
    ], 
    "orthologs": [
        {
            "uniprot_canonical_ac": "Q99707-1", 
            "protein_name": "Methionine synthase", 
            "sequence": {
                "length": 1265, 
                "sequence": "MSPALQDLSQPEGLKKTLRDEINAILQKRIMVLDGGMGTMIQREKLNEEHFRGQEFKDHARPLKGNNDILSITQPDVIYQIHKEYLLAGADIIETNTFSSTSIAQADYGLEHLAYRMNMCSAGVARKAAEEVTLQTGIKRFVAGALGPTNKTLSVSPSVERPDYRNITFDELVEAYQEQAKGLLDGGVDILLIETIFDTANAKAALFALQNLFEEKYAPRPIFISGTIVDKSGRTLSGQTGEGFVISVSHGEPLCIGLNCALGAAEMRPFIEIIGKCTTAYVLCYPNAGLPNTFGDYDETPSMMAKHLKDFAMDGLVNIVGGCCGSTPDHIREIAEAVKNCKPRVPPATAFEGHMLLSGLEPFRIGPYTNFVNIGERCNVAGSRKFAKLIMAGNYEEALCVAKVQVEMGAQVLDVNMDDGMLDGPSAMTRFCNLIASEPDIAKVPLCIDSSNFAVIEAGLKCCQGKCIVNSISLKEGEDDFLEKARKIKKYGAAMVVMAFDEEGQATETDTKIRVCTRAYHLLVKKLGFNPNDIIFDPNILTIGTGMEEHNLYAINFIHATKVIKETLPGARISGGLSNLSFSFRGMEAIREAMHGVFLYHAIKSGMDMGIVNAGNLPVYDDIHKELLQLCEDLIWNKDPEATEKLLRYAQTQGTGGKKVIQTDEWRNGPVEERLEYALVKGIEKHIIEDTEEARLNQKKYPRPLNIIEGPLMNGMKIVGDLFGAGKMFLPQVIKSARVMKKAVGHLIPFMEKEREETRVLNGTVEEEDPYQGTIVLATVKGDVHDIGKNIVGVVLGCNNFRVIDLGVMTPCDKILKAALDHKADIIGLSGLITPSLDEMIFVAKEMERLAIRIPLLIGGATTSKTHTAVKIAPRYSAPVIHVLDASKSVVVCSQLLDENLKDEYFEEIMEEYEDIRQDHYESLKERRYLPLSQARKSGFQMDWLSEPHPVKPTFIGTQVFEDYDLQKLVDYIDWKPFFDVWQLRGKYPNRGFPKIFNDKTVGGEARKVYDDAHNMLNTLISQKKLRARGVVGFWPAQSIQDDIHLYAEAAVPQAAEPIATFYGLRQQAEKDSASTEPYYCLSDFIAPLHSGIRDYLGLFAVACFGVEELSKAYEDDGDDYSSIMVKALGDRLAEAFAEELHERVRRELWAYCGSEQLDVADLRRLRYKGIRPAPGYPSQPDHTEKLTMWRLADIEQSTGIRLTESLAMAPASAVSGLYFSNLKSKYFAVGKISKDQVEDYALRKNISVAEVEKWLGPILGYDTD"
            }, 
            "evidence": [
                {
                    "url": "http://www.informatics.jax.org/homology/37280", 
                    "id": "37280", 
                    "database": "MGI"
                }, 
                {
                    "url": "https://omabrowser.org/oma/group/A6H5Y3/", 
                    "id": "A6H5Y3", 
                    "database": "OMA"
                }
            ], 
            "common_name": "Human", 
            "organism": "Homo sapiens", 
            "gene_name": "MTR", 
            "tax_id": 9606
        }, 
        {
            "uniprot_canonical_ac": "Q9Z2Q4-1", 
            "protein_name": "Methionine synthase", 
            "sequence": {
                "length": 1253, 
                "sequence": "MKKTLQDEIEAILRKRIMVLDGGMGTMIQRYKLSEENFQGQEFKDHSRPLKGNNDILSITQPDVIYQIHKEYLLAGADIIETNTFSSTSIAQADYGLEHLAYRMNKCSADVARKAAEEITLQTGVKRFVAGSLGPTNKTLSVSPSVERPDYRNITFDELVEAYQEQAKGLLDGGVDILLIETIFDTANAKAALFALQKLFEENYASPRPIFISGTIVDKSGRTLSGQTGEAFVTSVSHSDPLCIGLNCALGAAEMRPFIETIGKCTTAYVLCYPNAGLPNTFGDYDETPAMMAMHLKDFAVDGLVNVVGGCCGSTPDHIREIAEAVKNCKPRVPPDSVFEGHMLLSGLEPFRIGPYTNFVNIGERCNVAGSKKFAKLIMAGNYEEALSVAKVQVEMGAQVLDINMDDGMLDGPSAMTKFCNFIASEPDIAKVPLCIDSSNFAVIEAGLKCCQGKCIVNSISLKEGEEDFLEKARKIKKFGAAVVVMAFDEEGQATETDVKVSVCTRAYHLLVEKVGFNPNDIIFDPNILTIGTGMEEHNLYAINFIHATRVIKETLPGVRISGGLSNLSFAFRGMDAIREAMHGVFLYHAIKFGMDMGIVNAGSLPVYDDIHKDLLQLCEDLIWNRDAEATEKLLRYAQTHGKGGKKVIQTDEWRNGSIEERLEYALVKGIEKHIVEDTEEARLNREKYPRPLNIIEGPLMNGMKVVGDLFGAGKMFLPQVIKSARVMKKAVGHLIPFMEKEREEARVLNGSVEEEDPYQGTIVLATVKGDVHDIGKNIVGVVLGCNNFRVIDLGVMTPCDKILQAALDHKADIIGLSGLITPSLDEMIFVAKEMERLAIKIPLLIGGATTSRTHTAVKIAPRYSAPVIHVLDASKSVVVCSQLLDENLKDDYFEEILEEYEDIRQDHYESLKERKYLPLSQARKHSFHIDWLSEPHPVKPTFIGTQVFEDYNLQKLVDYIDWKPFFDVWQLRGKYPNRGFPKIFNDKAVGEEARKVYEDAQNMLSILISRKKLRARGVVGFWPAQSVQDDIHLYAEGAVPQAAEPIATFYGLRQQAEKDSSSTDPYHCLSDFVAPLHSGVRDYLGLFAVACFGVEELSKAYEDDGDDYSSIMVKALGDRLAEAFAEELHERVRRELWAYCGSEQLGVTDLRKLRYEGIRPAPGYPSQPDHTEKLTMWRLANIEQATGIRLTESLAMAPASAVSGLYFSNVKSKYFAVGKISKDQIEDYALRKNMSVAEVEKWLGPILGYDTD"
            }, 
            "evidence": [
                {
                    "url": "http://www.informatics.jax.org/homology/37280", 
                    "id": "37280", 
                    "database": "MGI"
                }
            ], 
            "common_name": "Rat", 
            "organism": "Rattus norvegicus", 
            "gene_name": "Mtr", 
            "tax_id": 10116
        }
    ], 
    "interactions": [], 
    "synthesized_glycans": [], 
    "snv": [], 
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb", 
            "label": "Isoforms"
        }, 
        {
            "name": "homologset.mgi", 
            "label": "MGI Homologs"
        }, 
        {
            "name": "homologset.oma", 
            "label": "OMA Homologs"
        }
    ], 
    "refseq": {
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
        "ac": "NP_001074597.1", 
        "name": "methionine synthase", 
        "summary": ""
    }, 
    "go_annotation": {
        "categories": [
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008705", 
                        "pmid": "11158293", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "methionine synthase activity", 
                        "id": "GO:0008705"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008270", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "zinc ion binding", 
                        "id": "GO:0008270"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0016597", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "amino acid binding", 
                        "id": "GO:0016597"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008168", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "methyltransferase activity", 
                        "id": "GO:0008168"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005542", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "folic acid binding", 
                        "id": "GO:0005542"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031419", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cobalamin binding", 
                        "id": "GO:0031419"
                    }
                ], 
                "total": 6, 
                "name": "Molecular Function"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cytosol", 
                        "id": "GO:0005829"
                    }
                ], 
                "total": 1, 
                "name": "Cellular Component"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009086", 
                        "pmid": "11158293", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "methionine biosynthetic process", 
                        "id": "GO:0009086"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0009235", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cobalamin metabolic process", 
                        "id": "GO:0009235"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006479", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "protein methylation", 
                        "id": "GO:0006479"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048678", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "response to axon injury", 
                        "id": "GO:0048678"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0071732", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cellular response to nitric oxide", 
                        "id": "GO:0071732"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031103", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "axon regeneration", 
                        "id": "GO:0031103"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0046653", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "tetrahydrofolate metabolic process", 
                        "id": "GO:0046653"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006555", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "methionine metabolic process", 
                        "id": "GO:0006555"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0050667", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                                "id": "A6H5Y3", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "homocysteine metabolic process", 
                        "id": "GO:0050667"
                    }
                ], 
                "total": 9, 
                "name": "Biological Process"
            }
        ]
    }, 
    "gene_names": [
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A6H5Y3", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "AI894170; D830038K18Rik; M; MS"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A6H5Y3", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "Mtr"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
            "type": "recommended", 
            "resource": "UniProtKB", 
            "name": "Mtr"
        }
    ], 
    "pro_annotation": [], 
    "crossref": [
        {
            "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000021311", 
            "id": "ENSMUSG00000021311", 
            "database": "Bgee"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd02069", 
            "id": "cd02069", 
            "database": "CDD"
        }, 
        {
            "url": "https://www.ebi.ac.uk/chembldb/target/inspect/CHEMBL3188", 
            "id": "CHEMBL3188", 
            "database": "ChEMBL"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/gene/238505", 
            "id": "238505", 
            "database": "GeneID"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR000489", 
            "id": "IPR000489", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR003726", 
            "id": "IPR003726", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR003759", 
            "id": "IPR003759", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR004223", 
            "id": "IPR004223", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR006158", 
            "id": "IPR006158", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011005", 
            "id": "IPR011005", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR011822", 
            "id": "IPR011822", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR033706", 
            "id": "IPR033706", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036589", 
            "id": "IPR036589", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036594", 
            "id": "IPR036594", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR036724", 
            "id": "IPR036724", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR037010", 
            "id": "IPR037010", 
            "database": "InterPro"
        }, 
        {
            "url": "https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+mmu:238505", 
            "id": "mmu:238505", 
            "database": "KEGG Pathway"
        }, 
        {
            "url": "http://www.informatics.jax.org/marker/MGI:894292", 
            "id": "894292", 
            "database": "MGI"
        }, 
        {
            "url": "https://omabrowser.org/oma/group/ADCIAMS/", 
            "id": "ADCIAMS", 
            "database": "OMA"
        }, 
        {
            "url": "http://www.orthodb.org/?query=731388at2759", 
            "id": "731388at2759", 
            "database": "OrthoDB"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF00809", 
            "id": "PF00809", 
            "database": "Pfam"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF02310", 
            "id": "PF02310", 
            "database": "Pfam"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF02574", 
            "id": "PF02574", 
            "database": "Pfam"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF02607", 
            "id": "PF02607", 
            "database": "Pfam"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF02965", 
            "id": "PF02965", 
            "database": "Pfam"
        }, 
        {
            "url": "http://purl.obolibrary.org/obo/PR_PR_A6H5Y3", 
            "id": "PR_A6H5Y3", 
            "database": "PRO"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-156581", 
            "id": "R-MMU-156581", 
            "database": "Reactome"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-1614635", 
            "id": "R-MMU-1614635", 
            "database": "Reactome"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-196741", 
            "id": "R-MMU-196741", 
            "database": "Reactome"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_001074597.1", 
            "id": "NP_001074597.1", 
            "database": "RefSeq"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
            "id": "A6H5Y3", 
            "database": "UniProtKB"
        }
    ], 
    "expression_disease": [], 
    "glycosylation": [], 
    "mutagenesis": [], 
    "disease": [
        {
            "synonyms": [
                {
                    "id": "DOID:0050731", 
                    "url": "http://disease-ontology.org/term/DOID:0050731", 
                    "resource": "Disease Ontology", 
                    "name": "cobalamin deficiency", 
                    "description": ""
                }, 
                {
                    "id": "DOID:0050731", 
                    "url": "http://disease-ontology.org/term/DOID:0050731", 
                    "resource": "Disease Ontology", 
                    "name": "hypocobalaminemia", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:0050731", 
                "url": "http://disease-ontology.org/term/DOID:0050731", 
                "resource": "Disease Ontology", 
                "name": "vitamin B12 deficiency", 
                "description": "A vitamin metabolic disorder that results from low blood levels of vitamin B12."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/0050731#disease-associations", 
                    "id": "0050731", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "methylcobalamin deficiency type cblG", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "homocystinuria-megaloblastic anemia, cblG complementation type", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblG complementation type", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "functional methionine synthase deficiency type cblG", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "methylcobalamin deficiency Cbl G type", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "homocystinuria-megaloblastic anemia, cblG complementation type; HMAG", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "methionine synthase deficiency", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "methylcobalamin deficiency, cblG type", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "cblG", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "HMAG", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009609", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009609", 
                    "resource": "MONDO", 
                    "name": "homocystinuria due to defect in methylation Cbl g", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:0050733", 
                "url": "http://disease-ontology.org/term/DOID:0050733", 
                "resource": "Disease Ontology", 
                "name": "methylmalonic aciduria and homocystinuria type cblG", 
                "description": "A methylmalonic acidemia that is characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures, has_material_basis_in homozygous or compound heterozygous mutation in the MTR gene on chromosome 1q43 that causes an inborn error of vitamin B12 metabolism."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/0050733#disease-associations", 
                    "id": "0050733", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [], 
            "recommended_name": {
                "id": "DOID:0080016", 
                "url": "http://disease-ontology.org/term/DOID:0080016", 
                "resource": "Disease Ontology", 
                "name": "spina bifida", 
                "description": "A neural tube defect that is characterized by incomplete closing of the spine and membranes around the spinal cord during early development."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/0080016#disease-associations", 
                    "id": "0080016", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "DOID:10763", 
                    "url": "http://disease-ontology.org/term/DOID:10763", 
                    "resource": "Disease Ontology", 
                    "name": "HTN", 
                    "description": ""
                }, 
                {
                    "id": "DOID:10763", 
                    "url": "http://disease-ontology.org/term/DOID:10763", 
                    "resource": "Disease Ontology", 
                    "name": "High blood pressure", 
                    "description": ""
                }, 
                {
                    "id": "DOID:10763", 
                    "url": "http://disease-ontology.org/term/DOID:10763", 
                    "resource": "Disease Ontology", 
                    "name": "hyperpiesia", 
                    "description": ""
                }, 
                {
                    "id": "DOID:10763", 
                    "url": "http://disease-ontology.org/term/DOID:10763", 
                    "resource": "Disease Ontology", 
                    "name": "vascular hypertensive disorder", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:10763", 
                "url": "http://disease-ontology.org/term/DOID:10763", 
                "resource": "Disease Ontology", 
                "name": "hypertension", 
                "description": "An artery disease characterized by chronic elevated blood pressure in the arteries."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/10763#disease-associations", 
                    "id": "10763", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "bladder cancer", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm of the bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant bladder neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant tumor of the urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant tumor of urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm of bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant bladder tumor", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant urinary bladder neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant tumor of the bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "urinary bladder malignant neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm, urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant tumor of bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "cancer of urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm of urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm of the urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "tumor of the bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant tumor, urinary bladder", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant urinary bladder tumor", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "urinary bladder malignant tumor", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0001187", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187", 
                    "resource": "MONDO", 
                    "name": "malignant neoplasm, bladder", 
                    "description": ""
                }, 
                {
                    "id": "DOID:11054", 
                    "url": "http://disease-ontology.org/term/DOID:11054", 
                    "resource": "Disease Ontology", 
                    "name": "bladder cancer", 
                    "description": ""
                }, 
                {
                    "id": "DOID:11054", 
                    "url": "http://disease-ontology.org/term/DOID:11054", 
                    "resource": "Disease Ontology", 
                    "name": "tumor of the bladder", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:11054", 
                "url": "http://disease-ontology.org/term/DOID:11054", 
                "resource": "Disease Ontology", 
                "name": "urinary bladder cancer", 
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/11054#disease-associations", 
                    "id": "11054", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [], 
            "recommended_name": {
                "id": "DOID:114", 
                "url": "http://disease-ontology.org/term/DOID:114", 
                "resource": "Disease Ontology", 
                "name": "heart disease", 
                "description": "A cardiovascular system disease that involves the heart."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/114#disease-associations", 
                    "id": "114", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0020643", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0020643", 
                    "resource": "MONDO", 
                    "name": "autism susceptibility 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0020643", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0020643", 
                    "resource": "MONDO", 
                    "name": "AUTS1", 
                    "description": ""
                }, 
                {
                    "id": "DOID:12849", 
                    "url": "http://disease-ontology.org/term/DOID:12849", 
                    "resource": "Disease Ontology", 
                    "name": "Kanner's syndrome", 
                    "description": ""
                }, 
                {
                    "id": "DOID:12849", 
                    "url": "http://disease-ontology.org/term/DOID:12849", 
                    "resource": "Disease Ontology", 
                    "name": "autism", 
                    "description": ""
                }, 
                {
                    "id": "DOID:12849", 
                    "url": "http://disease-ontology.org/term/DOID:12849", 
                    "resource": "Disease Ontology", 
                    "name": "autistic disorder of childhood onset", 
                    "description": ""
                }, 
                {
                    "id": "DOID:12849", 
                    "url": "http://disease-ontology.org/term/DOID:12849", 
                    "resource": "Disease Ontology", 
                    "name": "childhood autism", 
                    "description": ""
                }, 
                {
                    "id": "DOID:12849", 
                    "url": "http://disease-ontology.org/term/DOID:12849", 
                    "resource": "Disease Ontology", 
                    "name": "infantile autism", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:12849", 
                "url": "http://disease-ontology.org/term/DOID:12849", 
                "resource": "Disease Ontology", 
                "name": "autistic disorder", 
                "description": "An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/12849#disease-associations", 
                    "id": "12849", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "Ca body of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "Ca head of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "Ca tail of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "malignant neoplasm of body of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "malignant neoplasm of head of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "malignant neoplasm of tail of pancreas", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "pancreas neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "pancreatic neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1793", 
                    "url": "http://disease-ontology.org/term/DOID:1793", 
                    "resource": "Disease Ontology", 
                    "name": "pancreatic tumor", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:1793", 
                "url": "http://disease-ontology.org/term/DOID:1793", 
                "resource": "Disease Ontology", 
                "name": "pancreatic cancer", 
                "description": "An endocrine gland cancer located_in the pancreas."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/1793#disease-associations", 
                    "id": "1793", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "IGAN1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "Igan", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "glomerulonephritis, IgA", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "IgA nephropathy, susceptibility to, 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "IgA nephropathy, susceptibility to, 1; IGAN1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "nephritis, IgA type", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008072", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008072", 
                    "resource": "MONDO", 
                    "name": "berger disease", 
                    "description": ""
                }, 
                {
                    "id": "DOID:2986", 
                    "url": "http://disease-ontology.org/term/DOID:2986", 
                    "resource": "Disease Ontology", 
                    "name": "Berger's IgA or IgG nephropathy", 
                    "description": ""
                }, 
                {
                    "id": "DOID:2986", 
                    "url": "http://disease-ontology.org/term/DOID:2986", 
                    "resource": "Disease Ontology", 
                    "name": "Focal Glomerulonephritis", 
                    "description": ""
                }, 
                {
                    "id": "DOID:2986", 
                    "url": "http://disease-ontology.org/term/DOID:2986", 
                    "resource": "Disease Ontology", 
                    "name": "IgA nephropathy", 
                    "description": ""
                }, 
                {
                    "id": "DOID:2986", 
                    "url": "http://disease-ontology.org/term/DOID:2986", 
                    "resource": "Disease Ontology", 
                    "name": "primary IgA nephropathy", 
                    "description": ""
                }, 
                {
                    "id": "DOID:2986", 
                    "url": "http://disease-ontology.org/term/DOID:2986", 
                    "resource": "Disease Ontology", 
                    "name": "segmental glomerulonephritis", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:2986", 
                "url": "http://disease-ontology.org/term/DOID:2986", 
                "resource": "Disease Ontology", 
                "name": "IgA glomerulonephritis", 
                "description": "A glomerulonephritis characterized by build up of IgA antibody in the glomerulus."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/2986#disease-associations", 
                    "id": "2986", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "RB1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "eye cancer, retinoblastoma", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "neuroblastoma of retina", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "retinoblastoma, malignant", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "retinoblastoma; RB1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "RB - retinoblastoma", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0008380", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0008380", 
                    "resource": "MONDO", 
                    "name": "Rb", 
                    "description": ""
                }, 
                {
                    "id": "DOID:768", 
                    "url": "http://disease-ontology.org/term/DOID:768", 
                    "resource": "Disease Ontology", 
                    "name": "RB", 
                    "description": ""
                }, 
                {
                    "id": "DOID:768", 
                    "url": "http://disease-ontology.org/term/DOID:768", 
                    "resource": "Disease Ontology", 
                    "name": "RB - Retinoblastoma", 
                    "description": ""
                }, 
                {
                    "id": "DOID:768", 
                    "url": "http://disease-ontology.org/term/DOID:768", 
                    "resource": "Disease Ontology", 
                    "name": "neuroblastoma of Retina", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:768", 
                "url": "http://disease-ontology.org/term/DOID:768", 
                "resource": "Disease Ontology", 
                "name": "retinoblastoma", 
                "description": "A retinal cell cancer and malignant neoplasm of retina and neuroblastoma and neuroendocrine tumors that derives_from the tissues of the retina."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/768#disease-associations", 
                    "id": "768", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [], 
            "recommended_name": {
                "id": "DOID:9279", 
                "url": "http://disease-ontology.org/term/DOID:9279", 
                "resource": "Disease Ontology", 
                "name": "hyperhomocysteinemia", 
                "description": "An amino acid metabolic disorder that involves an abnormally large level of homocysteine in the blood."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/9279#disease-associations", 
                    "id": "9279", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0011363", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363", 
                    "resource": "MONDO", 
                    "name": "diabetes mellitus, noninsulin-dependent, 3", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0011363", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363", 
                    "resource": "MONDO", 
                    "name": "NIDDM3", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0011363", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363", 
                    "resource": "MONDO", 
                    "name": "noninsulin-dependent diabetes mellitus 3", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0011363", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0011363", 
                    "resource": "MONDO", 
                    "name": "diabetes mellitus, noninsulin-dependent, type 3", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9352", 
                    "url": "http://disease-ontology.org/term/DOID:9352", 
                    "resource": "Disease Ontology", 
                    "name": "NIDDM", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9352", 
                    "url": "http://disease-ontology.org/term/DOID:9352", 
                    "resource": "Disease Ontology", 
                    "name": "non-insulin-dependent diabetes mellitus", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9352", 
                    "url": "http://disease-ontology.org/term/DOID:9352", 
                    "resource": "Disease Ontology", 
                    "name": "type 2 diabetes", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9352", 
                    "url": "http://disease-ontology.org/term/DOID:9352", 
                    "resource": "Disease Ontology", 
                    "name": "type II diabetes mellitus", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9352", 
                    "url": "http://disease-ontology.org/term/DOID:9352", 
                    "resource": "Disease Ontology", 
                    "name": "insulin resistance", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:9352", 
                "url": "http://disease-ontology.org/term/DOID:9352", 
                "resource": "Disease Ontology", 
                "name": "type 2 diabetes mellitus", 
                "description": "A diabetes mellitus that is characterized by high blood sugar, insulin resistance, and relative lack of insulin."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/9352#disease-associations", 
                    "id": "9352", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "plasma cell myeloma", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloma, plasma cell, malignant", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "medullary plasmacytoma", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloid neoplasm of plasma cell", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "amyloidosis, systemic", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloma, multiple", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "Al amyloidosis", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "plasma cell myeloid neoplasm", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myelomatosis", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "Kahler's disease", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "Kahler disease", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloma, NOS", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "multiple myeloma/plasma cell myeloma", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloma - multiple", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0009693", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0009693", 
                    "resource": "MONDO", 
                    "name": "myeloma", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9538", 
                    "url": "http://disease-ontology.org/term/DOID:9538", 
                    "resource": "Disease Ontology", 
                    "name": "plasma cell myeloma", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:9538", 
                "url": "http://disease-ontology.org/term/DOID:9538", 
                "resource": "Disease Ontology", 
                "name": "multiple myeloma", 
                "description": "A myeloid neoplasm that is located_in the plasma cells in bone marrow."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/9538#disease-associations", 
                    "id": "9538", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, acute lymphocytic, susceptibility to, 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, acute lymphoblastic, B-Hyperdiploid, susceptibility to", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, acute lymphoblastic; ALL", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "All1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, T-cell acute lymphoblastic, susceptibility to", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, acute lymphoblastic, susceptibility to, 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, B-cell acute lymphoblastic, susceptibility to", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "ALL", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0013108", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0013108", 
                    "resource": "MONDO", 
                    "name": "leukemia, acute lymphoblastic", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9952", 
                    "url": "http://disease-ontology.org/term/DOID:9952", 
                    "resource": "Disease Ontology", 
                    "name": "ALL", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9952", 
                    "url": "http://disease-ontology.org/term/DOID:9952", 
                    "resource": "Disease Ontology", 
                    "name": "precursor lymphoblastic lymphoma/leukemia", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9952", 
                    "url": "http://disease-ontology.org/term/DOID:9952", 
                    "resource": "Disease Ontology", 
                    "name": "acute lymphoblastic leukaemia", 
                    "description": ""
                }, 
                {
                    "id": "DOID:9952", 
                    "url": "http://disease-ontology.org/term/DOID:9952", 
                    "resource": "Disease Ontology", 
                    "name": "acute lymphocytic leukaemia", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:9952", 
                "url": "http://disease-ontology.org/term/DOID:9952", 
                "resource": "Disease Ontology", 
                "name": "acute lymphoblastic leukemia", 
                "description": "A acute leukemia that is characterized by over production of lymphoblasts."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/9952#disease-associations", 
                    "id": "9952", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }
    ], 
    "phosphorylation": [
        {
            "residue": "Thr", 
            "kinase_gene_name": "", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
                    "id": "A6H5Y3", 
                    "database": "UniProtKB"
                }
            ], 
            "start_pos": "1252", 
            "end_pos": "1252", 
            "kinase_uniprot_canonical_ac": ""
        }
    ], 
    "mass": {
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        "chemical_mass": 139069.0
    }, 
    "expression_tissue": [], 
    "gene": [
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3", 
            "name": "Mtr", 
            "locus": {
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                "strand": "-", 
                "start_pos": 12258113, 
                "chromosome": "13", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSG00000021311", 
                        "id": "ENSMUSG00000021311", 
                        "database": "Ensembl Gene"
                    }
                ]
            }
        }
    ], 
    "protein_names": [
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "2.1.1.13"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "5-methyltetrahydrofolate--homocysteine methyltransferase"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "Cobalamin-dependent methionine synthase"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "MS"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "recommended", 
            "resource": "UniProtKB", 
            "name": "Methionine synthase"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A6H5Y3#names_and_taxonomy", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "Vitamin-B12 dependent methionine synthase"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A6H5Y3", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "methionine synthase"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/A6H5Y3", 
            "type": "synonym", 
            "resource": "RefSeq", 
            "name": "vitamin-B12 dependent methionine synthase; cobalamin-dependent methionine synthase"
        }
    ]
}
