Evidence Details for MAGIX
Basic Information Top
| Gene Symbol: | MAGIX ( FLJ21687,JM10,MGC138889,PDZX ) |
|---|---|
| Gene Full Name: | MAGI family member, X-linked |
| Band: | Xp11.23 |
| Quick Links | Entrez ID:79917; OMIM: NA; Uniprot ID:MAGIX_HUMAN; ENSEMBL ID: ENSG00000017621; HGNC ID: 30006 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>MAGIX|79917|nucleotide
ATGTCCCCCAACAGCCCTCTCCACTGCTTTTATCTCCCAGCTGTTAGCGTGCTGGACTCTGCGGACATAGAGGTCACAGACAGTCGCCTGCCTCATGCCACTATT
GTGGATCACCGGCCCCAGGGTAAGGCACGTAGTGCTCCGAAGCCATCCCAGGCCTCTGGTCATTTCTCTGTGGAGCTGGTTCGCGGTTACGCAGGCTTTGGCCTC
ACCTTAGGTGGGGGCCGGGATGTAGCTGGGGACACTCCGCTGGCCGTGCGCGGGCTGCTGAAGGATGGCCCAGCACAGCGCTGTGGTCGTTTGGAGGTCGGGGAC
CTCGTGCTCCACATCAACGGAGAGTCAACGCAGGGCCTCACCCATGCCCAGGCCGTGGAGCGGATCCGAGCTGGAGGCCCCCAGCTCCACCTGGTTATTCGTCGG
CCTCTGGAGACCCACCCTGGCAAGCCTCGAGGGGTGGGAGAGCCCCGAAAAGGAGTTGATCGCAGCCCAGATCCTGGAGGGCCGGAGGTAACGGGGTCTCGCAGC
AGCAGCACTTCCCTAGTTCAGCACCCTCCATCCCGGACGACGCTCAAGAAGACCCGGGGCAGCCCGGAGCCTAGTCCAGAGGCGGCCGCCGATGGCCCCACGGTT
TCTCCTCCTGAGCGCCGCGCTGAGGATCCCAACGACCAGATCCCGGGTTCCCCGGGGCCCTGGCTAGTGCCCAGCGAGGAACGGCTCTCGCGGGCCCTAGGGGTC
CGGGGGGCAGCGCAGCTCGCTCAGGAGATGGCAGCCGGAAGGCGGAGACACTGA
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ATGTCCCCCAACAGCCCTCTCCACTGCTTTTATCTCCCAGCTGTTAGCGTGCTGGACTCTGCGGACATAGAGGTCACAGACAGTCGCCTGCCTCATGCCACTATT
GTGGATCACCGGCCCCAGGGTAAGGCACGTAGTGCTCCGAAGCCATCCCAGGCCTCTGGTCATTTCTCTGTGGAGCTGGTTCGCGGTTACGCAGGCTTTGGCCTC
ACCTTAGGTGGGGGCCGGGATGTAGCTGGGGACACTCCGCTGGCCGTGCGCGGGCTGCTGAAGGATGGCCCAGCACAGCGCTGTGGTCGTTTGGAGGTCGGGGAC
CTCGTGCTCCACATCAACGGAGAGTCAACGCAGGGCCTCACCCATGCCCAGGCCGTGGAGCGGATCCGAGCTGGAGGCCCCCAGCTCCACCTGGTTATTCGTCGG
CCTCTGGAGACCCACCCTGGCAAGCCTCGAGGGGTGGGAGAGCCCCGAAAAGGAGTTGATCGCAGCCCAGATCCTGGAGGGCCGGAGGTAACGGGGTCTCGCAGC
AGCAGCACTTCCCTAGTTCAGCACCCTCCATCCCGGACGACGCTCAAGAAGACCCGGGGCAGCCCGGAGCCTAGTCCAGAGGCGGCCGCCGATGGCCCCACGGTT
TCTCCTCCTGAGCGCCGCGCTGAGGATCCCAACGACCAGATCCCGGGTTCCCCGGGGCCCTGGCTAGTGCCCAGCGAGGAACGGCTCTCGCGGGCCCTAGGGGTC
CGGGGGGCAGCGCAGCTCGCTCAGGAGATGGCAGCCGGAAGGCGGAGACACTGA
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>MAGIX|79917|protein
MSPNSPLHCFYLPAVSVLDSADIEVTDSRLPHATIVDHRPQGKARSAPKPSQASGHFSVELVRGYAGFGLTLGGGRDVAGDTPLAVRGLLKDGPAQRCGRLEVGD
LVLHINGESTQGLTHAQAVERIRAGGPQLHLVIRRPLETHPGKPRGVGEPRKGVDRSPDPGGPEVTGSRSSSTSLVQHPPSRTTLKKTRGSPEPSPEAAADGPTV
SPPERRAEDPNDQIPGSPGPWLVPSEERLSRALGVRGAAQLAQEMAAGRRRH
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MSPNSPLHCFYLPAVSVLDSADIEVTDSRLPHATIVDHRPQGKARSAPKPSQASGHFSVELVRGYAGFGLTLGGGRDVAGDTPLAVRGLLKDGPAQRCGRLEVGD
LVLHINGESTQGLTHAQAVERIRAGGPQLHLVIRRPLETHPGKPRGVGEPRKGVDRSPDPGGPEVTGSRSSSTSLVQHPPSRTTLKKTRGSPEPSPEAAADGPTV
SPPERRAEDPNDQIPGSPGPWLVPSEERLSRALGVRGAAQLAQEMAAGRRRH
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Score (No. of Studies) | No | 0 (0) | 1 (5) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (5) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Marshall, 2008 | - | SNP microarray | ![]() | ![]() | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 |
| Edens, 2011 | Honduras | aCGH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Edens, 2011 | Austria | FISH, aCGH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Chung, 2011 | - | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 1 | - | 1 |
| Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
| Edens, 2011 | Honduras | aCGH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Edens, 2011 | Austria | FISH, aCGH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
Linkage Studies Top



