{
    "uniprot_canonical_ac": "A0A087WPF7-1", 
    "ptm_annotation": [], 
    "sequence": {
        "header": "sp|A0A087WPF7-1|AUTS2_MOUSE Isoform 1 of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=2 CANONICAL=A0A087WPF7-1", 
        "length": 1261, 
        "sequence": "MDGPTRGHGLRKKRRSRSQRDRERRSRAGLGTGAAGGIGAGRTRAPSLASSSGSDKEDNGKPPSSAPSRPRPPRRKRRESTSAEEDIIDGFAMTSFVTFEALEKDVAVKPQERAEKRQTPLTKKKREALTNGLSFHSKKSRLSHSHHYSSDRENDRNLCQHLGKRKKMPKGLRQLKPGQNSCRDSDSESASGESKGFQRSSSRERLSDSSAPSSLGTGYFCDSDSDQEEKASDASSEKLFNTVLVNKDPELGVGALPEHNQDAGPIVPKISGLERSQEKSQDCCKEPVFEPVVLKDPHPQLPQLPSQAQAEPQLQIPSPGPDLVPRTEAPPQFPPPSTQPAQGPPEAQLQPAPLPQVQQRPPRPQSPSHLLQQTLPPVQSHPSSQSLSQPLSAYNSSSLSLNSLSSRSSTPAKTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVPGHPAGSTYSEQDILRQELNTRFLASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPMIPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSVFGHKDSPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHPSHPSPAPPVPVSALGHNRSSTDPTTRGHLNTEAREKDKPKEKERDHSGSRKDLTTEEHKAKESHLPERDGHSHEGRAAGEEPKQLSRVPSPYVRTPGVDSTRPNSTSSREAEPRKGEPAYENPKKNAEVKVKEERKEDHDLPTEAPQAHRTSEAPPPSSSASASVHPGPLASMPMTVGVTGIHAMNSIGSLDRTRMVTPFMGLSPIPGGERFPYPSFHWDPMRDPLRDPYRDLDMHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLAVDPRREHERGGHLDERERLHVLREDYEHPRLHPVHPASLDGHLPHPSLLTPGLPSMHYPRISPTAGHQNGLLNKTPPTAALSAPPPLISTLGGRPGSPRRTTPLSAEIRERPPSHTLKDIEAR"
    }, 
    "uniprot_id": "AUTS2_MOUSE", 
    "enzyme_annotation": [], 
    "glycation": [], 
    "keywords": [], 
    "species": [
        {
            "common_name": "Mouse", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "name": "Mus musculus", 
            "taxid": 10090
        }
    ], 
    "publication": [
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/19948250", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "19948250"
                }
            ], 
            "title": "Autism susceptibility candidate 2 (Auts2) encodes a nuclear protein expressed in developing brain regions implicated in autism neuropathology.", 
            "journal": "Gene Expr. Patterns", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "authors": "Hevner R.F., Hodge R.D., Nelson B.R., Bedogni F., Daza R.A., Frederick E.A., Shiba N.", 
            "date": "2010"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/25519132", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "25519132"
                }
            ], 
            "title": "An AUTS2-polycomb complex activates gene expression in the CNS.", 
            "journal": "Nature", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "authors": "Reinberg D., Schaefer A., Gao Z., Lee P., Stafford J.M., von Schimmelmann M.", 
            "date": "2014"
        }, 
        {
            "reference": [
                {
                    "url": "https://www.ncbi.nlm.nih.gov/pubmed/25533347", 
                    "type": [
                        "PubMed"
                    ], 
                    "id": "25533347"
                }
            ], 
            "title": "Cytoskeletal regulation by AUTS2 in neuronal migration and neuritogenesis.", 
            "journal": "Cell Rep.", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "authors": "Abe M., Nagai T., Yamada K., Yamazaki M., Kaibuchi K., Hayashi T., Hori K., Nakao K., Sakamoto A., Taya S., Hashimoto R., Hoshino M., Sakimura K., Nishioka T., Shan W.", 
            "date": "2014"
        }
    ], 
    "uniprot_ac": "A0A087WPF7", 
    "site_annotation": [
        {
            "end_pos": 1213, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 1211
        }, 
        {
            "end_pos": 397, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 395
        }, 
        {
            "end_pos": 438, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 436
        }, 
        {
            "end_pos": 786, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 784
        }, 
        {
            "end_pos": 870, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 868
        }, 
        {
            "end_pos": 957, 
            "annotation": "n_glycosylation_sequon", 
            "start_pos": 955
        }
    ], 
    "isoforms": [
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#A0A087WPF7-1", 
            "isoform_ac": "A0A087WPF7-1", 
            "locus": {}, 
            "sequence": {
                "header": "sp|A0A087WPF7-1|AUTS2_MOUSE Isoform 1 of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=2 CANONICAL=A0A087WPF7-1", 
                "length": 1261, 
                "sequence": "MDGPTRGHGLRKKRRSRSQRDRERRSRAGLGTGAAGGIGAGRTRAPSLASSSGSDKEDNGKPPSSAPSRPRPPRRKRRESTSAEEDIIDGFAMTSFVTFEALEKDVAVKPQERAEKRQTPLTKKKREALTNGLSFHSKKSRLSHSHHYSSDRENDRNLCQHLGKRKKMPKGLRQLKPGQNSCRDSDSESASGESKGFQRSSSRERLSDSSAPSSLGTGYFCDSDSDQEEKASDASSEKLFNTVLVNKDPELGVGALPEHNQDAGPIVPKISGLERSQEKSQDCCKEPVFEPVVLKDPHPQLPQLPSQAQAEPQLQIPSPGPDLVPRTEAPPQFPPPSTQPAQGPPEAQLQPAPLPQVQQRPPRPQSPSHLLQQTLPPVQSHPSSQSLSQPLSAYNSSSLSLNSLSSRSSTPAKTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVPGHPAGSTYSEQDILRQELNTRFLASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPMIPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSVFGHKDSPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHPSHPSPAPPVPVSALGHNRSSTDPTTRGHLNTEAREKDKPKEKERDHSGSRKDLTTEEHKAKESHLPERDGHSHEGRAAGEEPKQLSRVPSPYVRTPGVDSTRPNSTSSREAEPRKGEPAYENPKKNAEVKVKEERKEDHDLPTEAPQAHRTSEAPPPSSSASASVHPGPLASMPMTVGVTGIHAMNSIGSLDRTRMVTPFMGLSPIPGGERFPYPSFHWDPMRDPLRDPYRDLDMHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLAVDPRREHERGGHLDERERLHVLREDYEHPRLHPVHPASLDGHLPHPSLLTPGLPSMHYPRISPTAGHQNGLLNKTPPTAALSAPPPLISTLGGRPGSPRRTTPLSAEIRERPPSHTLKDIEAR"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#A0A087WPF7-2", 
            "isoform_ac": "A0A087WPF7-2", 
            "locus": {}, 
            "sequence": {
                "header": "sp|A0A087WPF7-2|AUTS2_MOUSE Isoform 2 of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=2 CANONICAL=A0A087WPF7-1", 
                "length": 258, 
                "sequence": "MDGPTRGHGLRKKRRSRSQRDRERRSRAGLGTGAAGGIGAGRTRAPSLASSSGSDKEDNGKPPSSAPSRPRPPRRKRRESTSAEEDIIDGFAMTSFVTFEALEKDVAVKPQERAEKRQTPLTKKKREALTNGLSFHSKKSRLSHSHHYSSDRENDRNLCQHLGKRKKMPKGLRQLKPGQNSCRDSDSESASGESKGFQRSSSRERLSDSSAPSSLGTGYFCDSDSDQEEKVRRHPLHCKHNPQGSGCTVTCLLVPVPL"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#A0A087WPF7-3", 
            "isoform_ac": "A0A087WPF7-3", 
            "locus": {
                "end_pos": 131439439, 
                "strand": "+", 
                "start_pos": 131475016, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000161374", 
                        "id": "ENSMUST00000161374", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000124730", 
                        "id": "ENSMUSP00000124730", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "sp|A0A087WPF7-3|AUTS2_MOUSE Isoform 3 of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=2 CANONICAL=A0A087WPF7-1", 
                "length": 789, 
                "sequence": "MFAPPTALPPPPPLTSGSLQVPGHPAGSTYSEQDILRQELNTRFLASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMLFHSYPPAVSGIPPMIPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSVFGHKDSPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHPSHPSPAPPVPVSALGHNRSSTDPTTRGHLNTEAREKDKPKEKERDHSGSRKDLTTEEHKAKESHLPERDGHSHEGRAAGEEPKQLSRVPSPYVRTPGVDSTRPNSTSSREAEPRKGEPAYENPKKNAEVKVKEERKEDHDLPTEAPQAHRTSEAPPPSSSASASVHPGPLASMPMTVGVTGIHAMNSIGSLDRTRMVTPFMGLSPIPGGERFPYPSFHWDPMRDPLRDPYRDLDMHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLAVDPRREHERGGHLDERERLHVLREDYEHPRLHPVHPASLDGHLPHPSLLTPGLPSMHYPRISPTAGHQNGLLNKTPPTAALSAPPPLISTLGGRPGSPRRTTPLSAEIRERPPSHTLKDIEAR"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#A0A087WSK2-1", 
            "isoform_ac": "A0A087WSK2-1", 
            "locus": {
                "end_pos": 132030909, 
                "strand": "+", 
                "start_pos": 132050409, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000185450", 
                        "id": "ENSMUST00000185450", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000141082", 
                        "id": "ENSMUSP00000141082", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A087WSK2-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=1 CANONICAL=A0A087WPF7-1", 
                "length": 48, 
                "sequence": "LKPGQNSCRDSDSESASGESKGFQRSSSRERLSDSSAPSSLGTGYFCE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#A0A2C9F2I4-1", 
            "isoform_ac": "A0A2C9F2I4-1", 
            "locus": {
                "end_pos": 131439439, 
                "strand": "+", 
                "start_pos": 131477024, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000187544", 
                        "id": "ENSMUST00000187544", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000139759", 
                        "id": "ENSMUSP00000139759", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|A0A2C9F2I4-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=1 CANONICAL=A0A087WPF7-1", 
                "length": 1013, 
                "sequence": "DPELGVGALPEHNQDAGPIVPKISGLERSQEKSQDCCKEPVFEPVVLKDPHPQLPQLPSQAQAEPQLQIPSPGPDLVPRTEAPPQFPPPSTQPAQGPPEAQLQPAPLQVQQRPPRPQSPSHLLQQTLPPVQSHPSSQSLSQPLSAYNSSSLSLNSLSSRSSTPAKTQPAPPHISHHPSASPFPLSLPNHSPLHSFTPTLQPPAHSHHPNMFAPPTALPPPPPLTSGSLQVPGHPAGSTYSEQDILRQELNTRFLASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPMIPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSVFGHKDSPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHPSHPSPAPPVPVSALGHNRSSTDPTTRGHLNTEAREKDKPKEKERDHSGSRKDLTTEEHKAKESHLPERDGHSHEGRAAGEEPKQLSRVPSPYVRTPGVDSTRPNSTSSREAEPRKGEPAYENPKKNAEVKVKEERKEDHDLPTEAPQAHRTSEAPPPSSSASASVHPGPLASMPMTVGVTGIHAMNSIGSLDRTRMVTPFMGLSPIPGGERFPYPSFHWDPMRDPLRDPYRDLDMHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLAVDPRREHERGGHLDERERLHVLREDYEHPRLHPVHPASLDGHLPHPSLLTPGLPSMHYPRISPTAGHQNGLLNKTPPTAALSAPPPLISTLGGRPGSPRRTTPLSAEIRERPPSHTLKDIEAR"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#E0CZ47-1", 
            "isoform_ac": "E0CZ47-1", 
            "locus": {
                "end_pos": 132030990, 
                "strand": "+", 
                "start_pos": 132449124, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000160135", 
                        "id": "ENSMUST00000160135", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000125706", 
                        "id": "ENSMUSP00000125706", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|E0CZ47-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=2 CANONICAL=A0A087WPF7-1", 
                "length": 119, 
                "sequence": "MMKDVAVKPQERAEKRQTPLTKKKREALTNGLSFHSKKSRLSHSHHYSSDRENDRNLCQHLGKRKKMPKGLRQLKPGQNSCRDSDSESASGESKGFQRSSSRERLSDSSAPSSLGTGYF"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#E9PZ86-1", 
            "isoform_ac": "E9PZ86-1", 
            "locus": {
                "end_pos": 131439439, 
                "strand": "+", 
                "start_pos": 131475016, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000161804", 
                        "id": "ENSMUST00000161804", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000124027", 
                        "id": "ENSMUSP00000124027", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|E9PZ86-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=1 CANONICAL=A0A087WPF7-1", 
                "length": 804, 
                "sequence": "MFAPPTALPPPPPLTSGSLQVPGHPAGSTYSEQDILRQELNTRFLASQSADRGASLGPPPYLRTEFHQHQHQHQHTHQHTHQHTFTPFPHAIPPTAIMPTPAPPMFDKYPTKVDPFYRHSLFHSYPPAVSGIPPMIPPTGPFGSLQGAFQPKTSNPIDVAARPGTVPHTLLQKDPRLTDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTPNSVFGHKDSPSVQNFSNPHEPWNRLHRTPPSFPTPPPWLKPGELERSASAAAHDRDRDVDKRDSSVSKDDKERESVEKRHPSHPSPAPPVPVSALGHNRSSTDPTTRGHLNTEAREKDKPKEKERDHSGSRKDLTTEEHKAKESHLPERDGHSHEGRAAGEEPKQLSRVPSPYVRTPGVDSTRPNSTSSREAEPRKGEPAYENPKKNAEVKVKEERKEDHDLPTEAPQAHRTSEAPPPSSSASASVHPGPLASMPMTVGVTGIHAMNSIGSLDRTRMVTPFMGLSPIPGGERFPYPSFHWDPMRDPLRDPYRDLDMHRRDPLGRDFLLRNDPLHRLSTPRLYEADRSFRDREPHDYSHHHHHHHHPLAVDPRREHERGGHLDERERLHVLREDYEHPRLHPVHPASLDGHLPHPSLLTPGLPSMHYPRISPTAGHQNGLLNKTPPTAALSAPPPLISTLGGRPGSPRRTTPLSAEIRERPPSHTLKDIEAR"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#J3QNT9-1", 
            "isoform_ac": "J3QNT9-1", 
            "locus": {
                "end_pos": 132541515, 
                "strand": "+", 
                "start_pos": 132541823, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000178555", 
                        "id": "ENSMUST00000178555", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000136954", 
                        "id": "ENSMUSP00000136954", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|J3QNT9-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=1 CANONICAL=A0A087WPF7-1", 
                "length": 103, 
                "sequence": "MDGPTRGHGLRKKRRSRSQRDRERRSRAGLGTGAAGGIGAGRTRAPSLASSSGSDKEDNGKPPSSAPSRPRPPRRKRRESTSAEEDIIDGFAMTSFVTFEALE"
            }
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#S4R200-1", 
            "isoform_ac": "S4R200-1", 
            "locus": {
                "end_pos": 131443781, 
                "strand": "+", 
                "start_pos": 131460151, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUST00000162101", 
                        "id": "ENSMUST00000162101", 
                        "database": "Ensembl Transcript"
                    }, 
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSP00000138441", 
                        "id": "ENSMUSP00000138441", 
                        "database": "Ensembl Peptide"
                    }
                ]
            }, 
            "sequence": {
                "header": "tr|S4R200-1|AUTS2_MOUSE Computationally mapped isoform of Autism susceptibility gene 2 protein homolog  OS=Mus musculus OX=10090 GN=Auts2 PE=1 SV=1 CANONICAL=A0A087WPF7-1", 
                "length": 142, 
                "sequence": "XDPFRPMLRKPGKWCAMHVHIAWQIYHHQQKVKKQMQSDPHKLDFGLKPEFLSRPPGPSLFGAIHHPHDLARPSTLFSAAGAAHPTGTPFGPPPHHSNFLNPAAHLEPFNRPSTFTGLAAVGGNAFGGLGNPSVTANNMYSF"
            }
        }
    ], 
    "pathway": [
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-8939243", 
            "resource": "Reactome", 
            "id": "R-MMU-8939243", 
            "name": "RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known"
        }
    ], 
    "function": [
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#function", 
            "annotation": "Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. The PRC1-like complex that contains PCGF5, RNF2, CSNK2B, RYBP and AUTS2 has decreased histone H2A ubiquitination activity, due to the phosphorylation of RNF2 by CSNK2B. As a consequence, the complex mediates transcriptional activation (By similarity). In the cytoplasm, plays a role in axon and dendrite elongation and in neuronal migration during embryonic brain development. Promotes reorganization of the actin cytoskeleton, lamellipodia formation and neurite elongation via its interaction with RAC guanine nucleotide exchange factors, which then leads to the activation of RAC1 (PubMed:25533347).", 
            "evidence": [
                {
                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7#function", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ]
        }
    ], 
    "orthologs": [], 
    "interactions": [], 
    "synthesized_glycans": [], 
    "snv": [], 
    "cluster_types": [
        {
            "name": "isoformset.uniprotkb", 
            "label": "Isoforms"
        }
    ], 
    "refseq": {}, 
    "go_annotation": {
        "categories": [
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0003682", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "chromatin binding", 
                        "id": "GO:0003682"
                    }
                ], 
                "total": 1, 
                "name": "Molecular Function"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "nucleus", 
                        "id": "GO:0005634"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005634", 
                        "pmid": "19948250", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "nucleus", 
                        "id": "GO:0005634"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0030426", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "growth cone", 
                        "id": "GO:0030426"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005737", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cytoplasm", 
                        "id": "GO:0005737"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0005856", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "cytoskeleton", 
                        "id": "GO:0005856"
                    }
                ], 
                "total": 5, 
                "name": "Cellular Component"
            }, 
            {
                "go_terms": [
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0001764", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "neuron migration", 
                        "id": "GO:0001764"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0060013", 
                        "pmid": "25519132", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "righting reflex", 
                        "id": "GO:0060013"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0031532", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "actin cytoskeleton reorganization", 
                        "id": "GO:0031532"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0035022", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "positive regulation of Rac protein signal transduction", 
                        "id": "GO:0035022"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0010592", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "positive regulation of lamellipodium assembly", 
                        "id": "GO:0010592"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0048675", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "axon extension", 
                        "id": "GO:0048675"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0097484", 
                        "pmid": "25533347", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "dendrite extension", 
                        "id": "GO:0097484"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0098582", 
                        "pmid": "25519132", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "innate vocalization behavior", 
                        "id": "GO:0098582"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0045944", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "positive regulation of transcription by RNA polymerase II", 
                        "id": "GO:0045944"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:0051571", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "positive regulation of histone H3-K4 methylation", 
                        "id": "GO:0051571"
                    }, 
                    {
                        "url": "https://www.ebi.ac.uk/QuickGO/term/GO:2000620", 
                        "pmid": "", 
                        "evidence": [
                            {
                                "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                                "id": "A0A087WPF7", 
                                "database": "UniProtKB"
                            }
                        ], 
                        "name": "positive regulation of histone H4-K16 acetylation", 
                        "id": "GO:2000620"
                    }
                ], 
                "total": 11, 
                "name": "Biological Process"
            }
        ]
    }, 
    "gene_names": [
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
            "type": "recommended", 
            "resource": "UniProtKB", 
            "name": "Auts2"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
            "type": "synonym", 
            "resource": "UniProtKB", 
            "name": "Kiaa0442"
        }
    ], 
    "pro_annotation": [], 
    "crossref": [
        {
            "url": "https://bgee.org/?page=gene&gene_id=ENSMUSG00000029673", 
            "id": "ENSMUSG00000029673", 
            "database": "Bgee"
        }, 
        {
            "url": "https://www.ebi.ac.uk/interpro/entry/IPR023246", 
            "id": "IPR023246", 
            "database": "InterPro"
        }, 
        {
            "url": "http://www.informatics.jax.org/marker/MGI:1919847", 
            "id": "1919847", 
            "database": "MGI"
        }, 
        {
            "url": "http://www.pantherdb.org/panther/family.do?clsAccession=PTHR14429", 
            "id": "PTHR14429", 
            "database": "PANTHER"
        }, 
        {
            "url": "http://pfam.xfam.org/family/PF15336", 
            "id": "PF15336", 
            "database": "Pfam"
        }, 
        {
            "url": "http://purl.obolibrary.org/obo/PR_PR_A0A087WPF7", 
            "id": "PR_A0A087WPF7", 
            "database": "PRO"
        }, 
        {
            "url": "https://www.reactome.org/PathwayBrowser/#R-MMU-8939243", 
            "id": "R-MMU-8939243", 
            "database": "Reactome"
        }, 
        {
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_796021.2", 
            "id": "NP_796021.2", 
            "database": "RefSeq"
        }, 
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
            "id": "A0A087WPF7", 
            "database": "UniProtKB"
        }
    ], 
    "expression_disease": [], 
    "glycosylation": [], 
    "mutagenesis": [], 
    "disease": [
        {
            "synonyms": [
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "intellectual disability, autosomal dominant 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in MBD5", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant 1; MRD1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "autosomal dominant mental retardation 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "autosomal dominant non-syndromic intellectual disability 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant type 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "chromosome 2Q23.1 deletion syndrome", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "MBD5 autosomal dominant non-syndromic intellectual disability", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant 1", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0007974", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
                    "resource": "MONDO", 
                    "name": "MRD1", 
                    "description": ""
                }, 
                {
                    "id": "DOID:0060307", 
                    "url": "http://disease-ontology.org/term/DOID:0060307", 
                    "resource": "Disease Ontology", 
                    "name": "autosomal dominant mental retardation", 
                    "description": ""
                }, 
                {
                    "id": "DOID:0060307", 
                    "url": "http://disease-ontology.org/term/DOID:0060307", 
                    "resource": "Disease Ontology", 
                    "name": "autosomal dominant non-syndromic mental retardation", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:0060307", 
                "url": "http://disease-ontology.org/term/DOID:0060307", 
                "resource": "Disease Ontology", 
                "name": "autosomal dominant non-syndromic intellectual disability", 
                "description": "A non-syndromic intellectual disability characterized by an autosomal dominant inheritance pattern."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/0060307#disease-associations", 
                    "id": "0060307", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "autism spectrum disorder due to AUTS2 deficiency", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant 26; MRD26", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "MRD26", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant 26", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "mental retardation, autosomal dominant type 26", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "ASD due to AUTS2 deficiency", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "autosomal dominant mental retardation 26", 
                    "description": ""
                }, 
                {
                    "id": "MONDO:0014361", 
                    "url": "https://monarchinitiative.org/disease/MONDO:0014361", 
                    "resource": "MONDO", 
                    "name": "AUTS2 syndrome", 
                    "description": ""
                }, 
                {
                    "id": "DOID:0070056", 
                    "url": "http://disease-ontology.org/term/DOID:0070056", 
                    "resource": "Disease Ontology", 
                    "name": "MRD26", 
                    "description": ""
                }, 
                {
                    "id": "DOID:0070056", 
                    "url": "http://disease-ontology.org/term/DOID:0070056", 
                    "resource": "Disease Ontology", 
                    "name": "autosomal dominant mental retardation 26", 
                    "description": ""
                }
            ], 
            "recommended_name": {
                "id": "DOID:0070056", 
                "url": "http://disease-ontology.org/term/DOID:0070056", 
                "resource": "Disease Ontology", 
                "name": "autosomal dominant non-syndromic intellectual disability 26", 
                "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of AUTS2 on chromosome 7q11.22."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/0070056#disease-associations", 
                    "id": "0070056", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }, 
        {
            "synonyms": [
                {
                    "id": "DOID:1574", 
                    "url": "http://disease-ontology.org/term/DOID:1574", 
                    "resource": "Disease Ontology", 
                    "name": "Ethanol abuse", 
                    "description": ""
                }, 
                {
                    "id": "DOID:1574", 
                    "url": "http://disease-ontology.org/term/DOID:1574", 
                    "resource": "Disease Ontology", 
                    "name": "alcohol abuse", 
                    "description": ""
                }
            ], 
            "recommended_name": {
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                "url": "http://disease-ontology.org/term/DOID:1574", 
                "resource": "Disease Ontology", 
                "name": "alcohol use disorder", 
                "description": "A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences."
            }, 
            "evidence": [
                {
                    "url": "https://www.alliancegenome.org/gene/1574#disease-associations", 
                    "id": "1574", 
                    "database": "Alliance of Genome Resources"
                }
            ]
        }
    ], 
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        {
            "residue": "Ser", 
            "kinase_gene_name": "", 
            "evidence": [
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                    "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "start_pos": "1200", 
            "end_pos": "1200", 
            "kinase_uniprot_canonical_ac": ""
        }, 
        {
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                    "id": "A0A087WPF7", 
                    "database": "UniProtKB"
                }
            ], 
            "start_pos": "1235", 
            "end_pos": "1235", 
            "kinase_uniprot_canonical_ac": ""
        }
    ], 
    "mass": {
        "monoisotopic_mass": 138920.0, 
        "chemical_mass": 138920.0
    }, 
    "expression_tissue": [], 
    "gene": [
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7", 
            "name": "Auts2", 
            "locus": {
                "end_pos": 131437333, 
                "strand": "-", 
                "start_pos": 132543344, 
                "chromosome": "5", 
                "evidence": [
                    {
                        "url": "https://www.ensembl.org/id/ENSMUSG00000029673", 
                        "id": "ENSMUSG00000029673", 
                        "database": "Ensembl Gene"
                    }
                ]
            }
        }
    ], 
    "protein_names": [
        {
            "url": "https://www.uniprot.org/uniprot/A0A087WPF7#names_and_taxonomy", 
            "type": "recommended", 
            "resource": "UniProtKB", 
            "name": "Autism susceptibility gene 2 protein homolog"
        }
    ]
}
