{ "uniprot_canonical_ac": "A0A0G2JZP7-1", "uniprot_ac": "A0A0G2JZP7", "uniprot_id": "A0A0G2JZP7_RAT", "mass": { "chemical_mass": 273939.0, "monoisotopic_mass": 273939.0 }, "refseq": { "ac": "XP_006234917", "name": "spatacsin", "summary": "", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917" }, "gene_names": [ { "name": "Spg11", "resource": "UniProtKB", "type": "recommended", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7", "id": "A0A0G2JZP7" }, { "name": "RGD1562529", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917", "id": "XP_006234917" }, { "name": "Spg11", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917", "id": "XP_006234917" } ], "protein_names": [ { "name": "SPG11 vesicle trafficking associated, spatacsin", "resource": "UniProtKB", "type": "synonym", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JZP7/entry#names_and_taxonomy", "id": "A0A0G2JZP7" }, { "name": "spastic paraplegia 11 (autosomal recessive); SPG11, spatacsin vesicle trafficking associated", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917", "id": "XP_006234917" }, { "name": "spatacsin", "resource": "RefSeq", "type": "synonym", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917", "id": "XP_006234917" } ], "function": [], "disease": [ { "disease_id": "DOID:0060197", "recommended_name": { "id": "DOID:0060197", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0060197", "name": "amyotrophic lateral sclerosis type 5", "description": "An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21." }, "synonyms": [ { "id": "DOID:0060197", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0060197", "name": "ALS5", "description": "" }, { "id": "DOID:0060197", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0060197", "name": "amyotrophic lateral sclerosis 5", "description": "" }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "amyotrophic lateral sclerosis type 5", "description": "Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the SPG11 gene." }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "ALS5", "description": "" }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "SPG11 amyotrophic lateral sclerosis", "description": "" }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "amyotrophic lateral sclerosis 5", "description": "" }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "amyotrophic lateral sclerosis caused by mutation in SPG11", "description": "" }, { "id": "MONDO:0011196", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011196", "name": "amyotrophic lateral sclerosis 5, juvenile", "description": "" }, { "id": "MIM:602099", "resource": "MIM", "url": "https://www.omim.org/entry/602099", "name": "Amyotrophic lateral sclerosis 5, juvenile", "description": "Amyotrophic lateral sclerosis 5, juvenile" } ], "evidence": [ { "id": "0060197", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0060197" } ] }, { "disease_id": "DOID:0110176", "recommended_name": { "id": "DOID:0110176", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110176", "name": "Charcot-Marie-Tooth disease axonal type 2X", "description": "A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or compound heterozygous mutation in the SPG11 gene on chromosome 15q21." }, "synonyms": [ { "id": "DOID:0110176", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110176", "name": "autosomal recessive axonal Charcot-Marie-Tooth disease type 2X", "description": "" }, { "id": "DOID:0110176", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110176", "name": "Charcot-Marie-Tooth neuropathy type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth disease axonal type 2X", "description": "Any Charcot-Marie-Tooth disease in which the cause of the disease is a mutation in the SPG11 gene." }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "ARCMT2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "CMT2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth disease caused by mutation in SPG11", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth disease, axonal, type 2x", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth neuropathy type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "SPG11 Charcot-Marie-Tooth disease", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "autosomal recessive axonal Charcot-Marie-Tooth disease type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth disease, axonal, type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "Charcot-Marie-Tooth neuropathy, type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "autosomal recessive Charcot Marie Tooth disease type 2X", "description": "" }, { "id": "MONDO:0014726", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0014726", "name": "autosomal recessive Charcot-Marie-Tooth disease type 2X", "description": "" }, { "id": "MIM:616668", "resource": "MIM", "url": "https://www.omim.org/entry/616668", "name": "Charcot-Marie-Tooth disease, axonal, 2X", "description": "Charcot-Marie-Tooth disease, axonal, 2X" } ], "evidence": [ { "id": "0110176", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0110176" } ] }, { "disease_id": "DOID:0110764", "recommended_name": { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "hereditary spastic paraplegia 11", "description": "A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21." }, "synonyms": [ { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "HSP-TCC", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "Nakamura-Osame syndrome", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "SPG11", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "autosomal recessive spastic paraplegia 11", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "autosomal recessive spastic paraplegia type 11", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "autosomal recessive spastic paraplegia complicated with thin corpus callosum", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "spastic paraplegia-intellectual disability-thin corpus callosum syndrome", "description": "" }, { "id": "DOID:0110764", "resource": "Disease Ontology", "url": "http://disease-ontology.org/term/DOID:0110764", "name": "autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "hereditary spastic paraplegia 11", "description": "Any hereditary spastic paraplegia in which the cause of the disease is a mutation in the SPG11 gene." }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "HSP-TCC", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "Nakamura-Osame syndrome", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "SPG11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "SPG11 hereditary spastic paraplegia", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "autosomal recessive spastic paraplegia 11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "autosomal recessive spastic paraplegia complicated with thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "autosomal recessive spastic paraplegia type 11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "hereditary spastic paraplegia caused by mutation in SPG11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "hereditary spastic paraplegia type 11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia-intellectual disability-thin corpus callosum syndrome", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "Nakamura Osame syndrome", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "hereditary spastic paraplegia mental impairment and thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia - intellectual deficit - thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia 11", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia 11, autosomal recessive", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum", "description": "" }, { "id": "MONDO:0011445", "resource": "MONDO", "url": "https://monarchinitiative.org/disease/MONDO:0011445", "name": "spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum", "description": "" }, { "id": "MIM:604360", "resource": "MIM", "url": "https://www.omim.org/entry/604360", "name": "Spastic paraplegia 11, autosomal recessive", "description": "Spastic paraplegia 11, autosomal recessive" } ], "evidence": [ { "id": "0110764", "database": "Alliance of Genome Resources", "url": "https://www.alliancegenome.org/disease/DOID:0110764" } ] } ], "snv": [], "mutagenesis": [], "expression_tissue": [], "expression_disease": [], "species": [ { "name": "Rattus norvegicus", "taxid": 10116, "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "common_name": "Rat", "glygen_name": "Rat", "reference_species": "Rattus norvegicus [10116]" } ], "gene": [ { "name": "Spg11", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7", "locus": { "chromosome": "3", "start_pos": 109008135, "end_pos": 109072911, "strand": "+", "evidence": [ { "database": "Ensembl Gene", "id": "ENSRNOG00000021954", "url": "https://www.ensembl.org/id/ENSRNOG00000021954" } ] } } ], "crossref": [ { "id": "A0A0G2JZP7", "url": "https://alphafold.ebi.ac.uk/entry/A0A0G2JZP7", "database": "AlphaFoldDB", "categories": [] }, { "id": "ENSRNOG00000021954", "url": "https://bgee.org/?page=gene&gene_id=ENSRNOG00000021954", "database": "Bgee", "categories": [ "Gene Expression" ] }, { "id": "IPR028103", "url": "https://www.ebi.ac.uk/interpro/entry/IPR028103", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "IPR028107", "url": "https://www.ebi.ac.uk/interpro/entry/IPR028107", "database": "InterPro", "categories": [ "Protein Classification" ] }, { "id": "AQWWDQL", "url": "https://omabrowser.org/oma/group/AQWWDQL/", "database": "OMA", "categories": [ "Protein Classification" ] }, { "id": "D3Z9Z3", "url": "https://www.orthodb.org/?gene=D3Z9Z3", "database": "OrthoDB", "categories": [ "Protein Classification" ] }, { "id": "PTHR13650", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13650", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PTHR13650:SF0", "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR13650:SF0", "database": "PANTHER", "categories": [ "Protein Classification" ] }, { "id": "PF14649", "url": "https://www.ebi.ac.uk/interpro/entry/pfam/PF14649", "database": "Pfam", "categories": [ "Protein Classification" ] }, { "id": "XP_006234917", "url": "https://www.ncbi.nlm.nih.gov/protein/XP_006234917", "database": "RefSeq", "categories": [ "Protein" ] }, { "id": "1562529", "url": "http://rgd.mcw.edu/tools/genes/genes_view.cgi?id=1562529", "database": "RGD", "categories": [ "Organism-specific" ] }, { "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A0G2JZP7-1", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A8I6G5Q3", "url": "https://www.uniprot.org/uniprot/A0A8I6G5Q3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "A0A8I6G5Q3-1", "url": "https://www.uniprot.org/uniprot/A0A8I6G5Q3-1", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D3Z9Z3", "url": "https://www.uniprot.org/uniprot/D3Z9Z3", "database": "UniProtKB", "categories": [ "Protein" ] }, { "id": "D3Z9Z3-1", "url": "https://www.uniprot.org/uniprot/D3Z9Z3-1", "database": "UniProtKB", "categories": [ "Protein" ] } ], "sequence": { "sequence": "MAAKPGPGSAASPGCAGAMERVLPMLLVRIPAEETAQLGPRAQLHRELEALGSLTAAGSLQVLSLAPGSRGGSSCRLQGPFRQFLWEESQNSTSADKPRVLVAREDCGLLIYEFDLRDGRCDAALLHSCCGRTLQKLTEDQGVSISFKSLRILSFDNSTSLLLINECLVVRVVFPGRESGIGVLGCLSLPLPAQAVDTIIDVQLCKRFLFLLSTLGWIHIFDTVKGMHVARVDLALPREDSEQQEPASISSFMSLKVSRDLDVLLLVSSSSTAVALNLHLYFRLHPGHLLCEGTLQDLPIEGPTGIDEDDLVNSAHNMKLTKVSFQVDRSWRAQLASLNESVRSSEPELSCYPPWFQGALCLESLESGNHSPIVPNHVFIPGDVPSGQYAFPQKEHSKTSEPRPWRTMHLSEQEQPTELTCLSVTGFTALFIQAVGTTSCTVVLWDLETQSMQCFSLSQKCTPVDISGDQQLCLALTENGLSLILFGLTQEEFLNRLMIHGSASTVDSLCHLNGWGRCSIPIHALEAGIENRQLDTVDFFLKSKENLLTPSSKSPAPDQQQHFSSQLYLRQVEEMTPALDLLCSAIRESDSETQSKHFAEQLLHLTLSFLNKQMRELFDHTEELDEHLQKGAAILTSYINELRTFMIKFPWKPGDAIDESDENEEVLTVKEGQVWEELRSEEVIADAILNNRIPEAQTFFRITGHSAQRLEELVRIGLDLAFDSLKKNSVEEASRLLRNMGFSVEDELLKISFYTTDKNIRDFLVEILKEKECFSEKERRTVDFVHQAERLYSGHFQENAPMQAFPRYWIKEQDCFKHKSVLDTFLKCDTKDEFTKQDHRIALNWAHWWDRQTQECILLPRISSEEYKAHSPEALWRHLTARHDWSSISLWMEEFQAQETVSPQQSKWPPLSAAVIEQNTCCSRHMRNAILDQLARCGIFLASELEDFELLLLRLSRIGGVMQDALPVQSYRSSAGCNFDSQVILYCLEHGLQHLLYVYLDYYKLSPGNCPFLEKKELHEAHPWLEFLVQCRQVSSNLTDPKLIFQASLANAQISIPTNQASVSSMLLEGHTLLALATTMYAPGGVSQVIQHEDSENCLKKVDPQLLKMALTPYPKLKAALFPQCTAPSILPSDITLYHLIQSLPPFDPSRLFGWQSANTLAIGDAAGQLPHFSSPDLVSKYAVVEQLSYTYYLHHGRPSFAFGTFLVQELIKSKTPKQLIQQVGKEAYTLGLSSFHNPSVGAACVCFLELLGLSSLKLRVDLKMANVVLGSRRRNEDAHPSFIRESLAEKLSKLADGDRATTEELLVLLEEGVWDSIEQQGFNRLSSESSSQWSLVLQFCMLHDMKLSVSYLRECAKANDWLQFLVHSQLHNYHPEEVETLLQYFSPVLQSHLKLASEKLSSGSISKDDSCLQELQKNKETSDFFEILHRCSDESASWCWLLAEAVRHRVPILSVLASCIQGASAVPCLCVWIVTSVEDKVAAEAIEHIQISVEDHHWSLEDLSIIWRTVLTRRKIHTLIRGFRLFIKDSPLLLIMEMYELCVFFKNYGKAKVKLVEFQKSLEMLDTVATRVLPVIPATWMREQVCFLLKLMPQQCETQYELQKVLQLFVGMEQLFSDGPDVQKLYRLSQVLKDTPITISPAVISSYSTESLQRECRSILEKLKADGQFAVARRVAELASLPVDGLVIEQLTQEMQMLTHTQQWSLKQARLDFWRKCHENFKKNSVSNRAASSFFSSQAPEASEHPAEQGSLEERHLLLTLAGHWLAQEEPVPVEELEELEKQIWLCRIAQHTCGGAEEETKPSLSQHKLAPAELSSDSSASEFSFSKLAALNTSKYLDLNGLPSKEMCENTLEHREQESLNTLIGQLLDGGCVHEASRVCRYFRVYSQDLVLLLHCRALASAEASMEDLHSEIRALLSNATLPEDLESPGVPLRKVHSTSSLDSLSFAMVPPTDEVARSLQTLISRCLHGKDYCRQVLCLYELAKELGCSYGDVATRDSEAMLRAILASQRPDRCRQAQVFINTQGLEPDTVAELVAEEVTRELLTPSEGAGEKQPFNLAEESQTFLQLTALCQDRTLVGMKLLDKIPSVPHGELSCTTELLILAHHCFTCACYMEGIIRVLQAARMLTDNHLAPNEEYGLVVRLLTGIGRYNEMTYIFDLLHQKHYFEVLMRKKLDPTGTLKTALLDYIKRCHPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLKDGAQLKQLLLKALTLMLDAAESYAKDSCVRQALHCNRLTKLITLQIHFLNSGQNTMLINLGHQKLMDCIMTLPRFYQASIVAEAYDFVPDWAEVLYQQVILKGDFSYLEEFKQQKLLKPNIFEDISKKYKQHQPTDRVTENLKKLLSYCEDIYLYYKLAYEHKFFEIVNMLLKDPQTGCCLKDMLAG", "length": 2428, "header": "tr|A0A0G2JZP7-1|A0A0G2JZP7_RAT Isoform 1 of SPG11 vesicle trafficking associated, spatacsin OS=Rattus norvegicus OX=10116 GN=Spg11 PE=4 SV=2 CANONICAL=A0A0G2JZP7-1" }, "isoforms": [ { "isoform_ac": "A0A0G2JZP7-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JZP7/entry#A0A0G2JZP7-1", "sequence": { "sequence": "MAAKPGPGSAASPGCAGAMERVLPMLLVRIPAEETAQLGPRAQLHRELEALGSLTAAGSLQVLSLAPGSRGGSSCRLQGPFRQFLWEESQNSTSADKPRVLVAREDCGLLIYEFDLRDGRCDAALLHSCCGRTLQKLTEDQGVSISFKSLRILSFDNSTSLLLINECLVVRVVFPGRESGIGVLGCLSLPLPAQAVDTIIDVQLCKRFLFLLSTLGWIHIFDTVKGMHVARVDLALPREDSEQQEPASISSFMSLKVSRDLDVLLLVSSSSTAVALNLHLYFRLHPGHLLCEGTLQDLPIEGPTGIDEDDLVNSAHNMKLTKVSFQVDRSWRAQLASLNESVRSSEPELSCYPPWFQGALCLESLESGNHSPIVPNHVFIPGDVPSGQYAFPQKEHSKTSEPRPWRTMHLSEQEQPTELTCLSVTGFTALFIQAVGTTSCTVVLWDLETQSMQCFSLSQKCTPVDISGDQQLCLALTENGLSLILFGLTQEEFLNRLMIHGSASTVDSLCHLNGWGRCSIPIHALEAGIENRQLDTVDFFLKSKENLLTPSSKSPAPDQQQHFSSQLYLRQVEEMTPALDLLCSAIRESDSETQSKHFAEQLLHLTLSFLNKQMRELFDHTEELDEHLQKGAAILTSYINELRTFMIKFPWKPGDAIDESDENEEVLTVKEGQVWEELRSEEVIADAILNNRIPEAQTFFRITGHSAQRLEELVRIGLDLAFDSLKKNSVEEASRLLRNMGFSVEDELLKISFYTTDKNIRDFLVEILKEKECFSEKERRTVDFVHQAERLYSGHFQENAPMQAFPRYWIKEQDCFKHKSVLDTFLKCDTKDEFTKQDHRIALNWAHWWDRQTQECILLPRISSEEYKAHSPEALWRHLTARHDWSSISLWMEEFQAQETVSPQQSKWPPLSAAVIEQNTCCSRHMRNAILDQLARCGIFLASELEDFELLLLRLSRIGGVMQDALPVQSYRSSAGCNFDSQVILYCLEHGLQHLLYVYLDYYKLSPGNCPFLEKKELHEAHPWLEFLVQCRQVSSNLTDPKLIFQASLANAQISIPTNQASVSSMLLEGHTLLALATTMYAPGGVSQVIQHEDSENCLKKVDPQLLKMALTPYPKLKAALFPQCTAPSILPSDITLYHLIQSLPPFDPSRLFGWQSANTLAIGDAAGQLPHFSSPDLVSKYAVVEQLSYTYYLHHGRPSFAFGTFLVQELIKSKTPKQLIQQVGKEAYTLGLSSFHNPSVGAACVCFLELLGLSSLKLRVDLKMANVVLGSRRRNEDAHPSFIRESLAEKLSKLADGDRATTEELLVLLEEGVWDSIEQQGFNRLSSESSSQWSLVLQFCMLHDMKLSVSYLRECAKANDWLQFLVHSQLHNYHPEEVETLLQYFSPVLQSHLKLASEKLSSGSISKDDSCLQELQKNKETSDFFEILHRCSDESASWCWLLAEAVRHRVPILSVLASCIQGASAVPCLCVWIVTSVEDKVAAEAIEHIQISVEDHHWSLEDLSIIWRTVLTRRKIHTLIRGFRLFIKDSPLLLIMEMYELCVFFKNYGKAKVKLVEFQKSLEMLDTVATRVLPVIPATWMREQVCFLLKLMPQQCETQYELQKVLQLFVGMEQLFSDGPDVQKLYRLSQVLKDTPITISPAVISSYSTESLQRECRSILEKLKADGQFAVARRVAELASLPVDGLVIEQLTQEMQMLTHTQQWSLKQARLDFWRKCHENFKKNSVSNRAASSFFSSQAPEASEHPAEQGSLEERHLLLTLAGHWLAQEEPVPVEELEELEKQIWLCRIAQHTCGGAEEETKPSLSQHKLAPAELSSDSSASEFSFSKLAALNTSKYLDLNGLPSKEMCENTLEHREQESLNTLIGQLLDGGCVHEASRVCRYFRVYSQDLVLLLHCRALASAEASMEDLHSEIRALLSNATLPEDLESPGVPLRKVHSTSSLDSLSFAMVPPTDEVARSLQTLISRCLHGKDYCRQVLCLYELAKELGCSYGDVATRDSEAMLRAILASQRPDRCRQAQVFINTQGLEPDTVAELVAEEVTRELLTPSEGAGEKQPFNLAEESQTFLQLTALCQDRTLVGMKLLDKIPSVPHGELSCTTELLILAHHCFTCACYMEGIIRVLQAARMLTDNHLAPNEEYGLVVRLLTGIGRYNEMTYIFDLLHQKHYFEVLMRKKLDPTGTLKTALLDYIKRCHPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLKDGAQLKQLLLKALTLMLDAAESYAKDSCVRQALHCNRLTKLITLQIHFLNSGQNTMLINLGHQKLMDCIMTLPRFYQASIVAEAYDFVPDWAEVLYQQVILKGDFSYLEEFKQQKLLKPNIFEDISKKYKQHQPTDRVTENLKKLLSYCEDIYLYYKLAYEHKFFEIVNMLLKDPQTGCCLKDMLAG", "length": 2428, "header": "tr|A0A0G2JZP7-1|A0A0G2JZP7_RAT Isoform 1 of SPG11 vesicle trafficking associated, spatacsin OS=Rattus norvegicus OX=10116 GN=Spg11 PE=4 SV=2 CANONICAL=A0A0G2JZP7-1" }, "locus": { "chromosome": "3", "start_pos": 109072839, "end_pos": 109008219, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000080253.2", "url": "https://www.ensembl.org/id/ENSRNOT00000080253.2" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000071131.2", "url": "https://www.ensembl.org/id/ENSRNOP00000071131.2" } ] } }, { "isoform_ac": "A0A8I6G5Q3-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JZP7/entry#A0A8I6G5Q3-1", "sequence": { "sequence": "MAAKPGPGSAASPGCAGAMERVLPMLLVRIPAEETAQLGPRAQLHRELEALGSLTAAGSLQVLSLAPGSRGGSSCRLQGPFRQFLWEESQNSTSADKPRVLVAREDCGLLIYEFDLRDGRCDAALLHSCCGRTLQKLTEDQGVSISFKSLRILSFDNSTSLLLINECLVVRVVFPGRESGIGVLGCLSLPLPAQAVDTIIDVQLCKRFLFLLSTLGWIHIFDTVKGMHVARVDLALPREDSEQQEPASISSFMSLKVSRDLDVLLLVSSSSTAVALNLHLYFRLHPGHLLCEGTLQDLPIEGPTGIDEDDLVNSAHNMKLTKVSFQVDRSWRAQLASLNESVRSSEPELSCYPPWFQGALCLESLESGNHSPIVPNHVFIPGDVPSGQYAFPQKEHSKTSEPRPWRTMHLSEQEQPTELTCLSVTGFTALFIQAVGTTSCTVVLWDLETQSMQCFSLSQKCTPVDISGDQQLCLALTENGLSLILFGLTQEEFLNRLMIHGSASTVDSLCHLNGWGRCSIPIHALEAGIENRQLDTVDFFLKSKENLLTPSSKSPAPDQQQHFSSQLYLRQVEEMTPALDLLCSAIRESDSETQSKHFAEQLLHLTLSFLNKQMRELFDHTEELDEHLQKGAAILTSYINELRTFMIKFPWKPGDAIDESDENEEVLTVKEGQVWEELRSEEVIADAILNNRIPEAQTFFRITGHSAQRLEELVRIGLDLAFDSLKKNSVEEASRLLRNMGFSVEDELLKISFYTTDKNIRDFLVEILKEKECFSEKERRTVDFVHQAERLYSGHFQENAPMQAFPRYWIKEQDCFKHKSVLDTFLKCDTKDEFTKQDHRIALNWAHWWDRQTQECILLPRISSEEYKAHSPEALWRHLTARHDWSSISLWMEEFQAQETVSPQQSKWPPLSAAVIEQNTCCSRHMRNAILDQLARCGIFLASELEDFELLLLRLSRIGGVMQDALPVQSYRSSAGCNFDSQVILYCLEHGLQHLLYVYLDYYKLSPGNCPFLEKKELHEAHPWLEFLVQCRQVSSNLTDPKLIFQASLANAQISIPTNQASVSSMLLEGHTLLALATTMYAPGGVSQSLPPFDPSRLFGWQSANTLAIGDAAGQLPHFSSPDLVSKYAVVEQLSYTYYLHHGRPSFAFGTFLVQELIKSKTPKQLIQQVGKEAYTLGLSSFHNPSVGAACVCFLELLGLSSLKLRVDLKMANVVLGSRRRNEDAHPSFIRESLAEKLSKLADGDRATTEELLVLLEEGVWDSIEQQGFNRLSSESSSQWSLVLQFCMLHDMKLSVSYLRECAKANDWLQFLVHSQLHNYHPEEVETLLQYFSPVLQSHLKLASEKLSSGSISKDDSCLQELQKNKETSDFFEILHRCSDESASWCWLLAEAVRHRVPILSVLASCIQGASAVPCLCVWIVTSVEDKVAAEAIEHIQISVEDHHWSLEDLSIIWRTVLTRRKIHTLIRGFRLFIKDSPLLLIMEMYELCVFFKNYGKAKVKLVEFQKSLEMLDTVATRVLPVIPATWMREQVCFLLKLMPQQCETQYELQKVLQLFVGMEQLFSDGPDVQKLYRLSQVLKDTPITISPAVISSYSTESLQRECRSILEKLKADGQFAVARRVAELASLPVDGLVIEQLTQEMQMLTHTQQWSLKQARLDFWRKCHENFKKNSVSNRAASSFFSSQAPEASEHPAEQGSLEERHLLLTLAGHWLAQEEPVPVEELEELEKQIWLCRIAQHTCGGAEEETKPSLSQHKLAPAELSSDSSASEFSFSKLAALNTSKYLDLNGLPSKEMCENTLEHREQESLNTLIGQLLDGGCVHEASRVCRYFRVYSQDLVLLLHCRALASAEASMEDLHSEIRALLSNATLPEDLESPGVPLRKVHSTSSLDSLSFAMVPPTDEVARSLQTLISRCLHGKDYCRQVLCLYELAKELGCSYGDVATRDSEAMLRAILASQRPDRCRQAQVFINTQGLEPDTVAELVAEEVTRELLTPSEGAGEKQPFNLAEESQTFLQLTALCQDRTLVGMKLLDKIPSVPHGELSCTTELLILAHHCFTCACYMEGIIRVLQAARMLTDNHLAPNEEYGLVVRLLTGIGRYNEMTYIFDLLHQKHYFEVLMRKKLDPTGTLKTALLDYIKRCHPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLKDGAQLKQLLLKALTLMLDAAESYAKDSCVRQALHCNRLTKLITLQIHFLNSGQNTMLINLGHQKLMDCIMTLPRFYQASIVAEAYDFVPDWAEVLYQQVILKGDFSYLEEFKQQKLLKPNIFEDISKKYKQHQPTDRVTENLKKLLSYCEDIYLYYKLAYEHKFFEIVNMLLKDPQTGCCLKDMLAG", "length": 2374, "header": "tr|A0A8I6G5Q3-1|A0A0G2JZP7_RAT Computationally mapped isoform of SPG11 vesicle trafficking associated, spatacsin OS=Rattus norvegicus OX=10116 GN=Spg11 PE=4 SV=1 CANONICAL=A0A0G2JZP7-1" }, "locus": { "chromosome": "3", "start_pos": 109072839, "end_pos": 109008219, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000097776.1", "url": "https://www.ensembl.org/id/ENSRNOT00000097776.1" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000081282.1", "url": "https://www.ensembl.org/id/ENSRNOP00000081282.1" } ] } }, { "isoform_ac": "D3Z9Z3-1", "url": "https://www.uniprot.org/uniprotkb/A0A0G2JZP7/entry#D3Z9Z3-1", "sequence": { "sequence": "MAAKPGPGSAASPGCAGAMERVLPMLLVRIPAEETAQLGPRAQLHRELEALGSLTAAGSLQVLSLAPGSRGGSSCRLQGPFRQFLWEESQNSTSADKPRVLVAREDCGLLIYEFDLRDGRCDAALLHSCCGRTLQKLTEDQGVSISFKSLRILSFDNSTSLLLINECLVVRVVFPGRESGIGVLGCLSLPLPAQAVDTIIDVQLCKRFLFLLSTLGWIHIFDTVKGMHVARVDLALPREDSEQQEPASISSFMSLKVSRDLDVLLLVSSSSTAVALNLHLYFRLHPGHLLCEGTLQDLPIEGPTGIDEDDLVNSAHNMKLTKVSFQVDRSWRAQLASLNESVRSSEPELSCYPPWFQGALCLESLESGNHSPIVPNHVFIPGDVPSGQYAFPQKEHSKTSEPRPWRTMHLSEQEQPTELTCLSVTGFTALFIQAVGTTSCTVVLWDLETQSMQCFSLSQKCTPVDISGDQQLCLALTENGLSLILFGLTQEEFLNRLMIHGSASTVDSLCHLNGWGRCSIPIHALEAGIENRQLDTVDFFLKSKENLLTPSSKSPAPDQQQHFSSQLYLRQVEEMTPALDLLCSAIRESDSETQSKHFAEQLLHLTLSFLNKQMRELFDHTEELDEHLQKGAAILTSYINELRTFMIKFPWKPGDAIDESDENEEVLTVKEGQVWEELRSEEVIADAILNNRIPEAQTFFRITGHSAQRLEELVRIGLDLAFDSLKKNSVEEASRLLRNMGFSVEDELLKISFYTTDKNIRDFLVEILKEKECFSEKERRTVDFVHQAERLYSGHFQENAPMQAFPRYWIKEQDCFKHKSVLDTFLKCDTKDEFTKQDHRIALNWAHWWDRQTQECILLPRISSEEYKAHSPEALWRHLTARHDWSSISLWMEEFQAQETVSPQQSKWPPLSAAVIEQNTCCSRHMRNAILDQLARCGIFLASELEDFELLLLRLSRIGGVMQDALPVQSYRSSAGCNFDSQVILYCLEHGLQHLLYVYLDYYKLSPGNCPFLEKKELHEAHPWLEFLVQCRQVSSNLTDPKLIFQASLANAQISIPTNQASVSSMLLEGHTLLALATTMYAPGGVSQVIQHEDSENCLKKVDPQLLKMALTPYPKLKAALFPQCTAPSILPSDITLYHLIQSLPPFDPSRLFGWQSANTLAIGDAAGQLPHFSSPDLVSKYAVVEQLSYTYYLHHGRPSFAFGTFLVQELIKSKTPKQLIQQVGKEAYTLGLSSFHNPSVGAACVCFLELLGLSSLKLRVDLKMANVVLGSRRRNEDAHPSFIRESLAEKLSKLADGDRATTEELLVLLEEGVWDSIEQQGFNRLSSESSSQWSLVLQFCMLHDMKLSVSYLRECAKANDWLQFLVHSQLHNYHPEEVETLLQYFSPVLQSHLKLASEKLSSGSISKDDSCLQELQKNKETSDFFEILHRCSDESASWCWLLAEAVRHRVPILSVLASCIQGASAVPCLCVWIVTSVEDKVAAEAIEHIQISVEDHHWSLEDLSIIWRTVLTRRKIHTLIRGFRLFIKDSPLLLIMEMYELCVFFKNYGKAKVKLVEFQKSLEMLDTVATRVLPVIPATWMREQVCFLLKLMPQQCETQYELQKVLQLFVGMEQLFSDGPDVQKLYRLSQVLKDTPITISPAVISSYSTESLQRECRSILEKLKADGQFAVARRVAELASLPVDGLVIEQLTQEMQMLTHTQQWSLKQARLDFWRKCHENFKKNSVSNRAASSFFSSQAPEASEHPAEQGSLEERHLLLTLAGHWLAQEEPVPVEELEELEKQIWLCRIAQHTCGGAEEETKPSLSQHKLAPAELSSDSSASEFSFSKLAALNTSKYLDLNGLPSKEMCENTLEHREQESLNTLIGQLLDGGCVHEASRVCRYFRVYSQDLVLLLHCRALASAEASMEDLHSEIRALLSNATLPEDLESPGVPLRKVHSREKQPFNLAEESQTFLQLTALCQDRTLVGMKLLDKIPSVPHGELSCTTELLILAHHCFTCACYMEGIIRVLQAARMLTDNHLAPNEEYGLVVRLLTGIGRYNEMTYIFDLLHQKHYFEVLMRKKLDPTGTLKTALLDYIKRCHPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLKDGAQLKQLLLKALTLMLDAAESYAKDSCVRQALHCNRLTKLITLQIHFLNSGQNTMLINLGHQKLMDCIMTLPRFYQASIVAEAYDFVPDWAEVLYQQVILKGDFSYLEEFKQQKLLKPNIFEDISKKYKQHQPTDRVTENLKKLLSYCEDIYLYYKLAYEHKFFEIVNMLLKDPQTGCCLKDMLAG", "length": 2315, "header": "tr|D3Z9Z3-1|A0A0G2JZP7_RAT Computationally mapped isoform of SPG11 vesicle trafficking associated, spatacsin OS=Rattus norvegicus OX=10116 GN=Spg11 PE=4 SV=2 CANONICAL=A0A0G2JZP7-1" }, "locus": { "chromosome": "3", "start_pos": 109072839, "end_pos": 109008219, "strand": "+", "evidence": [ { "database": "Ensembl Transcript", "id": "ENSRNOT00000022875.7", "url": "https://www.ensembl.org/id/ENSRNOT00000022875.7" }, { "database": "Ensembl Peptide", "id": "ENSRNOP00000022875.6", "url": "https://www.ensembl.org/id/ENSRNOP00000022875.6" } ] } } ], "glycosylation": [], "phosphorylation": [], "glycation": [], "keywords": [], "publication": [], "pathway": [], "orthologs": [ { "uniprot_canonical_ac": "A0A8V0Z1S5-1", "protein_name": "SPG11 vesicle trafficking associated, spatacsin", "gene_name": "SPG11", "tax_id": 9031, "organism": "Gallus gallus", "sequence": { "sequence": "MAGARRELRVLLAARPGQARDSVRDAARVRLSAEQDALGSLLLRDGIYLESLGPGGGGRARSGVLPGAWADFVWERTAEYDPQAKRTKILALSESHDLFVYEFTREDGKCGPDPLHSCREGVLKKLLEANSVSLSSILSLRILSFKDNKCTLLLNSFIVMHLTFPGEHSSLETCDCFTLDLPPPVLERVTDINFCRGILFFLDSSGWIYVFDSSDGANLAHINVSLCQGGVQDGDRSPTITSPLTALKVSYDLSVAVIISSSSNACSVDLNVYFRQFPGHLICRRDSESLSLKPPEGVDEDDLASSDYSMELLSSPFRTDRSWKAHLSSLCSTIRKRRSRSPHLLCDMNLPWYQYFTHLEDHDPLIYETSEKALAIAPKAFPPVLSNPSQSAGTKLSDMGQQWKQILPVQLSQEVVKLECKSVTGAKALFVILTDDKALTLALWDFESQDVAHYQFGKNSVYVDCNEEVPLCLLLTECGLSLILFGLTQEEFLNRLMIYGSAGVVDSVCHLNGWGRCSIPVHALEAGLENRQLDTVDLFLKSKESLFNLSALRSEAQQSADGASCSFLKNLQELRPALNLLCSAIRENDMEPQSKHFSEQLLNLTLTFLSKQLEEIFVHTEEPDRYLQKAAEILTDYIIELRTFMKNYPRSQVNTTNVGSDSDEDLPAIEESQMWEKLTPEEVIAEAILSNKMPEAQIFFRMHRHPAQSLQELIRTGLDLVYGHLLKGNTREASALLKNMGFDVKQQLHKICFYTADKHVRDLLVKVLQEENYFSEKEKKMIDFVHQVESLYSESFQENKEMQSLSSVRNWRQEQDSSKHLATLESLMDHDGRRVPSREVRVMLNWAQCWDELLQDMILLPRKQGQGLATCNPEALWMYLTAQHDWLNISSWIEEFEPNHSLCGQSKWPPLAASIIDQHTLCSGYMRNEILNKLARNGIFVLSELEDFELLLQRLVSLGGVLQNPHPVPKYSAASGLDFHARFILHCLEHNLQYMLYTYLDYYSLTPSNCPILDDKELHEAHPWFEFLVQCRGVASNPRDPKMIFQASLANAQILIPSNQASVSSMLLEGRTLLALATTMYAPGGIDQVLQNEDTEKPLKKVDPQLLKMALSPYPKLRAALFPPCTSHGILPPDISLYHLVQSLVPFDPSKLFGWQSTNTLAVSDASSDLPHFSSPELVNKYAVMERLDFLYYLRHGRPSFAFGTFLVQQLVKSKSPKQLIQQAGNEAYLLGLSFFNTPSVAAACVCFLELLGLSSLKLRVDIKVANMIFIYKTRNEETQHNQIRESLVEQLMRLADGEKAATEEVLKSLEEAFWDSIEHQGIKRTSSDSRQQWSLVMQFCKLHAMKLSTSYLKECAKSNDWLQFIIQAQLYSYKPDEVSSVLEGFAPIIQHHLMLALEKSPFLHAAAGAPEGSTGSRCADSLFQILFRCQESPNASCHLLAEGLREHAPILSVLAACSPDADIIHCLCVWIITSVDDVTRSEATKHIQSSVENHKWDLHDLSLIWKVLLRKQKCQTLIRGFQLFLKDSPLLHILEMYDLCMNCKRYYEAKTKLDEFQKHLINLKTTDGAAASGVPVQWLESQALFLLELMMQQCRTEYELGKLLQLFAATDNLLLDGPYVKKLCALSETLRDSSVPINRSMLTRYTPETFQKECTSILEQLQEKGMFSLAREVAELAELPADSVVTQEILRDIRLLRDTGEWDRDQIRIKFWKKCNDSFVKNSISSKAASDFFLNQGNVVSESPVREKINSISERHLLLTLAGHWLAKDVSVALDKLEEIEKQIWICRITQQMLSTDEGPGKSGRSSCAAANGDFTFDNLAKEFSFSKLPALNTPNYLNVEGLELRGCQQTLAAEEEESLRFLVGCLLDEGSVHEASRVCRYFHFYSRDVSLVLHCRALAAGEADLDRLHADIQALVAIEKTQDSSASQQSRVPSTSSLEDWTHIADPSPDDQIVVSLKALTDECVHGRNYCRQVLCLYELSKELNCSYSEMSALDPEKVLRAILSSQQAERCRRAQAFITTQGLQPETVAELVAKEVVQELLASSEGKGQKQVSNPAAESQAFLQLAKLCQDHTLVGMKLLEKISSVPRGELSCITELLILAHNCFSLTCHMEGITRVLQAARLLTDEHLAPNDEYGLMVRLLTGIGRYNEMTYIFELLHEKHYFEVLMRKKLDPSGTLKTALLDYIKRCRPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLQDVANLKKLLMKALTLFIDAAESYSKDSCVRQALRCRRLTKLITLQLHFLSTGQSTMLINRNRQNLMECIVSLPRFYQAAVVAEAYEFVPDWAEVLYQQVIAKGDFSYLEEFKQQRLLKPAMFEEIAKKCKQHPPSDAALRNLKKLLAYCEDISTYYRLAYDNKFYDVVNMLLKDAQTGCCLNDMLSS", "length": 2425 }, "evidence": [ { "id": "A0A0G2JZP7", "url": "https://omabrowser.org/oma/group/A0A0G2JZP7/", "database": "OMA" } ], "glygen_name": "Chicken", "common_name": "Chicken" }, { "uniprot_canonical_ac": "Q3UHA3-1", "protein_name": "Spatacsin", "gene_name": "Spg11", "tax_id": 10090, "organism": "Mus musculus", "sequence": { "sequence": "MAAQPGPGSAASPGCAGAMERVLPMLLVRIPAEETAQLGPRAQLHRELEALGSLTAAGSLQVLSLAPGSRGGSSCCLPGPFRQFLWEESQNSTSRDRPKLLVAREDYELLVYEFDLRDGRCDAALLHGCCGRTLQKLTEDQGVSISFKSLRILSFHNNTSLLLINRCLILRVVFPGKEPGVPVLDCLSLPLPAQAADMIIDAQLCERFLFVLSTVGLIYIFNTMDGTQVAQVDLALLREDSEQLEPASVSSFTSLRVSQDLDVLVLVSSASTAVALNLHLYFRQHPGHLLCEGTLEDLPIEGPPGIDEDDLVNSAHNMKLSKVSFQVDRSWRAQLLSLNESVRGSEPEVSCCAPWFQSALRLESLESADHTPTVPTHVFIPGDVPRGRCAFPQKEHVKSSDPGRPWKTMHLSEHEQPTELTCLSVTGFTALFTWAVGATSCTIGLWDLETQSMQCFSLSQKCTPVDIGGDQQLCLALTDDGLSLILFGLTQEEFLNRLMIHGSASTVDSLCHLNGWGRCSIPIHALEAGIENRQLDTVDFFLKSKENLLTPSSQSPAPDQQHPFSSHLYLRQVEEMSPALDLLCSAIRESDSETQSKHFAEQLLHLTLSFLNKQIRELCVHTEELDEHFQKGVAILTSYINELRTFMIKFPWKPGDAIDESDVNEGVVTVKEDRVWEELSFEEVIADAILNNRIPEAQTFFRISGHSAQRLEELVRIGLDLAFDSLKKNNVEEASRLLRNMGFSVEDELLKICFYTTDKNIRDFLVEILKEKECFSEKERRTVDFVHQLEALYSGHFQENAQTQAFPRYWIKEQDCFKHKSVLDTFLKYDKKDEFHKQDHRIALNWAHRWDLQTQECILLRRLSPEEYKARSPEALWRHLTARHDCSSISLWMEEFQTQETESPQQSKWPPLSADIIEQGTCCHSHMRNEILDKLARSGIFLASELEDFERLLLRLSRIGGVMQDSLPVQSYKSRAGCDFHSRFILYCLEHGLQHLLYTYLDYYKLSPGNCPFLEKKELHEAHPWLEFLVQCRQVSSNLTDPKLIFQASLANAQILIPTNQASVSSMLLEGHTLLALATTMYAPGGVSQVIQNEDSENCLKKVDPQLLKVALTPYPKLKAALFPQYTAPSILPSDITLYHLIQSLPPFDPSRLFVWQSANTLAIGDTGSQLPHFSSPDLVSKYAVLERLNYAYYLHHGRPSFAFGTFLVQELIKSKTPKQLIQQVGKEAYTLGLSSFTNPSVGAACVCFLELLGLSSLKLRVDLKMANVILGSKRRDEDARSSFIRESLAEKLSKLADGDRAATEELLVLLEEGVWDSIEQQGFSRLSSESSSQWALVLQFCMLHDRKLSVSYLRECAKANDWLQFLVHSQLHNYHPAEVESLLQYFSPVLQSHLKLASEKLSSGSISRDDSCLQELQKNKGETSNFFEILHRCSDESTSWSWLLAEAVRHRAPILSVLASCVQGASVVSCLCVWIVTSVEDKVAAEAMGHIQISVEDHHWSLKDLSIIWRTVLTRRKSHTLIRGFQLFIKDSPLLLIMEMYELCMFFKNYEKAKVKLLEFQKSLETLDTVAARVLPIIPASWMKDQVCFLLKLMPQQCETQYELGKLLQLFVGTEQLFSDGPDVQKLCLLSQVLKDTPIAISPAVISSYSTENFQRECRSILEKLKADGQFAVARRVAELAALPVDSLLIEQLTQEMQTLTHTPQWSLKQERLGFWKKCHEIFKKNSISKRAASSFFSSQAPEVSEHPAEQGSLEERHLLLTLAGHWLAQEEPVPVEELEGLEKQIWICRVAQHTCGGAEEEAKPSLSQHKLAAAELSFDSLASELSFSKLAALNTSKYLGLNDLPSKTTCENRLKHKEQESLNTLIGQLLDGGCVHEASRVCQYFRFYSQDLVLVLHCRALASAEATMEDLHSEIRALLSSAAQPEDLESPSVPLRKAHSSSSLDSQSFVMVPPTDEVAQNLHTLISKCLHGKNYCRQVLCLYELAKDLGCSYGDVAARDSEAMLRAILASQRPDRCRQAQVFINTQGLEADTVAELVAEEVTRELLTPSEGTGEKQPFNPAEESQTFLQLTALCQDRTLVGMKLLDKIPSVPHGELSCTTELLILAHHCFTFTCHMEGITRVLQAARMLTDNHLAPNEEYGLVVRLLTGIGRYNEMTYIFDLLHQKHYFEVLMRKKLDPTGTLKTALLDYIKRCRPGDSEKHNMIALCFSMCREIGENHEAAACIQLKLIESQPWEESLKDGAQLKQLLLKALTLMLDAAESYAKDSCVRQALHCNRLTKLITLQIHFLNSGQNTMLINLGHQKLMDCIMTLPRFYQASIVAEAYDFVPDWAEVLYQQVILKGDFSYLEEFKQQKLLRPNIFEDISKKYKQHQPTDRVTENLKKLLSYCEDIYLYYKLAYEHKFFEIVNMLLKDPQTGCCLKDMLAG", "length": 2430 }, "evidence": [ { "id": "A0A0G2JZP7", "url": "https://omabrowser.org/oma/group/A0A0G2JZP7/", "database": "OMA" } ], "glygen_name": "Mouse", "common_name": "Mouse" }, { "uniprot_canonical_ac": "Q96JI7-1", "protein_name": "Spatacsin", "gene_name": "SPG11", "tax_id": 9606, "organism": "Homo sapiens", "sequence": { "sequence": "MAAEEGVASAASAGGSWGTAAMGRVLPMLLVPVPAEAMGQLGSRAQLRTQPEALGSLTAAGSLQVLSLTPGSRGGGRCCLEGPFWHFLWEDSRNSSTPTEKPKLLALGENYELLIYEFNLKDGRCDATILYSCSREALQKLIDDQDISISLLSLRILSFHNNTSLLFINKCVILHIIFPERDAAIRVLNCFTLPLPAQAVDMIIDTQLCRGILFVLSSLGWIYIFDVVDGTYVAHVDLALHKEDMCNEQQQEPAKISSFTSLKVSQDLDVAVIVSSSNSAVALNLNLYFRQHPGHLLCERILEDLPIQGPKGVDEDDPVNSAYNMKLAKFSFQIDRSWKAQLSSLNETIKNSKLEVSCCAPWFQDILHLESPESGNHSTSVQSWAFIPQDIMHGQYNVLQKDHAKTSDPGRSWKIMHISEQEEPIELKCVSVTGFTALFTWEVERMGYTITLWDLETQGMQCFSLGTKCIPVDSSGDQQLCFVLTENGLSLILFGLTQEEFLNRLMIHGSASTVDTLCHLNGWGRCSIPIHALEAGIENRQLDTVNFFLKSKENLFNPSSKSSVSDQFDHLSSHLYLRNVEELIPALDLLCSAIRESYSEPQSKHFSEQLLNLTLSFLNNQIKELFIHTEELDEHLQKGVNILTSYINELRTFMIKFPWKLTDAIDEYDVHENVPKVKESNIWKKLSFEEVIASAILNNKIPEAQTFFRIDSHSAQKLEELIGIGLNLVFDNLKKNNIKEASELLKNMGFDVKGQLLKICFYTTNKNIRDFLVEILKEKNYFSEKEKRTIDFVHQVEKLYLGHFQENMQIQSFPRYWIKEQDFFKHKSVLDSFLKYDCKDEFNKQDHRIVLNWALWWDQLTQESILLPRISPEEYKSYSPEALWRYLTARHDWLNIILWIGEFQTQHSYASLQQNKWPLLTVDVINQNTSCNNYMRNEILDKLARNGVFLASELEDFECFLLRLSRIGGVIQDTLPVQNYKTKEGWDFHSQFILYCLEHSLQHLLYVYLDCYKLSPENCPFLEKKELHEAHPWFEFLVQCRQVASNLTDPKLIFQASLANAQILIPTNQASVSSMLLEGHTLLALATTMYSPGGVSQVVQNEENENCLKKVDPQLLKMALTPYPKLKTALFPQCTPPSVLPSDITIYHLIQSLSPFDPSRLFGWQSANTLAIGDAWSHLPHFSSPDLVNKYAIVERLNFAYYLHNGRPSFAFGTFLVQELIKSKTPKQLIQQVGNEAYVIGLSSFHIPSIGAACVCFLELLGLDSLKLRVDMKVANIILSYKCRNEDAQYSFIRESVAEKLSKLADGEKTTTEELLVLLEEGTWNSIQQQEIKRLSSESSSQWALVVQFCRLHNMKLSISYLRECAKANDWLQFIIHSQLHNYHPAEVKSLIQYFSPVIQDHLRLAFENLPSVPTSKMDSDQVCNKCPQELQGSKQEMTDLFEILLQCSEEPDSWHWLLVEAVKQQAPILSVLASCLQGASAISCLCVWIITSVEDNVATEAMGHIQDSTEDHTWNLEDLSVIWRTLLTRQKSKTLIRGFQLFFKDSPLLLVMEMYELCMFFRNYKEAEAKLLEFQKSLETLNTAATKVHPVIPAMWLEDQVCFLLKLMLQQCKTQYELGKLLQLFVEREHLFSDGPDVKKLCILCQILKDTSIAINHTIITSYSIENLQHECRSILERLQTDGQFALARRVAELAELPVDNLVIKEITQEMQTLKHIEQWSLKQARIDFWKKCHENFKKNSISSKAASSFFSTQAHVACEHPTGWSSMEERHLLLTLAGHWLAQEDVVPLDKLEELEKQIWLCRITQHTLGRNQEETEPRFSRQISTSGELSFDSLASEFSFSKLAALNTSKYLELNSLPSKETCENRLDWKEQESLNFLIGRLLDDGCVHEASRVCRYFHFYNPDVALVLHCRALASGEASMEDLHPEIHALLQSAELLEEEAPDIPLRRVHSTSSLDSQKFVTVPSSNEVVTNLEVLTSKCLHGKNYCRQVLCLYDLAKELGCSYTDVAAQDGEAMLRKILASQQPDRCKRAQAFISTQGLKPDTVAELVAEEVTRELLTSSQGTGHKQMFNPTEESQTFLQLTTLCQDRTLVGMKLLDKISSVPHGELSCTTELLILAHHCFTLTCHMEGIIRVLQAAHMLTDNHLAPSEEYGLVVRLLTGIGRYNEMTYIFDLLHKKHYFEVLMRKKLDPSGTLKTALLDYIKRCRPGDSEKHNMIALCFSMCREIGENHEAAARIQLKLIESQPWEDSLKDGHQLKQLLLKALTLMLDAAESYAKDSCVRQAQHCQRLTKLITLQIHFLNTGQNTMLINLGRHKLMDCILALPRFYQASIVAEAYDFVPDWAEILYQQVILKGDFNYLEEFKQQRLLKSSIFEEISKKYKQHQPTDMVMENLKKLLTYCEDVYLYYKLAYEHKFYEIVNVLLKDPQTGCCLKDMLAG", "length": 2443 }, "evidence": [ { "id": "A0A0G2JZP7", "url": "https://omabrowser.org/oma/group/A0A0G2JZP7/", "database": "OMA" } ], "glygen_name": "Human", "common_name": "Human" } ], "go_annotation": { "categories": [ { "name": "Cellular Component", "total": 8, "go_terms": [ { "name": "cytoplasm", "id": "GO:0005737", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "cytosol", "id": "GO:0005829", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005829", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "axon", "id": "GO:0030424", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030424", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "dendrite", "id": "GO:0030425", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030425", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "synapse", "id": "GO:0045202", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045202", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "cytoplasmic vesicle", "id": "GO:0031410", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031410", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "nucleolus", "id": "GO:0005730", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005730", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "plasma membrane", "id": "GO:0005886", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005886", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" } ] }, { "name": "Biological Process", "total": 20, "go_terms": [ { "name": "axonogenesis", "id": "GO:0007409", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007409", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "neuromuscular junction development", "id": "GO:0007528", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007528", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "memory", "id": "GO:0007613", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007613", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "axo-dendritic transport", "id": "GO:0008088", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0008088", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "neuron apoptotic process", "id": "GO:0051402", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051402", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "chemical synaptic transmission", "id": "GO:0007268", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007268", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "cholesterol efflux", "id": "GO:0033344", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0033344", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "skeletal muscle fiber development", "id": "GO:0048741", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048741", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "lysosome organization", "id": "GO:0007040", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0007040", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "axon extension", "id": "GO:0048675", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048675", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "autophagosome organization", "id": "GO:1905037", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:1905037", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "regulation of store-operated calcium entry", "id": "GO:2001256", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2001256", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "motor neuron apoptotic process", "id": "GO:0097049", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097049", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "phagosome-lysosome fusion involved in apoptotic cell clearance", "id": "GO:0090389", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090389", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "walking behavior", "id": "GO:0090659", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0090659", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "corticospinal tract morphogenesis", "id": "GO:0021957", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0021957", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "localization within membrane", "id": "GO:0051668", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051668", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "synaptic vesicle transport", "id": "GO:0048489", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048489", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "protein import into nucleus", "id": "GO:0006606", "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0006606", "evidence": [ { "database": "UniProtKB", "id": "A0A0G2JZP7", "url": "https://www.uniprot.org/uniprot/A0A0G2JZP7" } ], "pmid": "" }, { "name": "motor 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