Evidence Details for MPDZ
Basic Information Top
Gene Symbol: | MPDZ ( DKFZp781P216,FLJ25909,FLJ34626,FLJ90240,MUPP1 ) |
---|---|
Gene Full Name: | multiple PDZ domain protein |
Band: | 9p23 |
Quick Links | Entrez ID:8777; OMIM: 603785; Uniprot ID:MPDZ_HUMAN; ENSEMBL ID: ENSG00000107186; HGNC ID: 7208 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>MPDZ|8777|nucleotide
ATGTTGGAAGCCATTGACAAAAATCGGGCCCTGCATGCAGCAGAGCGCTTGCAAACCAAGCTGCGAGAACGTGGGGATGTAGCAAATGAAGACAAACTGAGCCTT
CTGAAGTCAGTCCTGCAGAGCCCTCTCTTCAGTCAGATTCTGAGCCTTCAGACTTCTGTACAGCAGCTGAAAGACCAGGTAAATATTGCAACTTCAGCAACTTCA
AATATTGAATATGCCCACGTTCCTCATCTCAGCCCAGCTGTGATTCCTACTCTGCAAAATGAATCGTTTTTATTATCCCCAAACAATGGGAATCTGGAAGCACTT
ACAGGACCTGGTATTCCACACATTAATGGGAAACCTGCTTGTGATGAATTTGATCAGCTTATCAAAAATATGGCCCAGGGTCGCCATGTAGAAGTTTTTGAGCTC
CTCAAACCTCCATCTGGAGGCCTTGGGTTTAGTGTTGTGGGACTAAGAAGTGAAAACAGAGGAGAGCTGGGAATATTTGTTCAAGAGATACAAGAGGGCAGTGTG
GCCCATAGAGATGGAAGATTGAAAGAAACTGATCAAATTCTTGCTATCAATGGACAGGCTCTTGATCAGACAATTACACATCAGCAGGCTATCAGCATCCTGCAG
AAAGCCAAAGATACTGTCCAGCTAGTTATTGCCAGAGGCTCATTGCCTCAGCTTGTCAGCCCCATAGTTTCCCGTTCTCCATCTGCAGCCAGCACAATTTCAGCT
CACTCTAATCCGGTTCACTGGCAACACATGGAAACGATTGAATTGGTGAATGATGGATCTGGTTTGGGATTTGGCATCATAGGAGGAAAAGCAACTGGTGTGATA
GTAAAAACCATTCTGCCTGGAGGAGTAGCTGATCAGCATGGGCGTTTATGCAGTGGAGACCACATTCTAAAGATTGGTGACACAGATCTAGCAGGAATGAGCAGT
GAGCAAGTAGCACAAGTCCTTAGGCAATGTGGAAATAGAGTTAAGTTGATGATTGCAAGAGGTGCCATAGAAGAACGTACAGCACCCACTGCTTTGGGCATCACC
CTCTCCTCATCCCCAACTTCAACACCAGAGTTGCGGGTTGATGCTTCTACTCAGAAAGGTGAAGAAAGTGAGACATTTGATGTAGAACTCACTAAAAATGTCCAA
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ATGTTGGAAGCCATTGACAAAAATCGGGCCCTGCATGCAGCAGAGCGCTTGCAAACCAAGCTGCGAGAACGTGGGGATGTAGCAAATGAAGACAAACTGAGCCTT
CTGAAGTCAGTCCTGCAGAGCCCTCTCTTCAGTCAGATTCTGAGCCTTCAGACTTCTGTACAGCAGCTGAAAGACCAGGTAAATATTGCAACTTCAGCAACTTCA
AATATTGAATATGCCCACGTTCCTCATCTCAGCCCAGCTGTGATTCCTACTCTGCAAAATGAATCGTTTTTATTATCCCCAAACAATGGGAATCTGGAAGCACTT
ACAGGACCTGGTATTCCACACATTAATGGGAAACCTGCTTGTGATGAATTTGATCAGCTTATCAAAAATATGGCCCAGGGTCGCCATGTAGAAGTTTTTGAGCTC
CTCAAACCTCCATCTGGAGGCCTTGGGTTTAGTGTTGTGGGACTAAGAAGTGAAAACAGAGGAGAGCTGGGAATATTTGTTCAAGAGATACAAGAGGGCAGTGTG
GCCCATAGAGATGGAAGATTGAAAGAAACTGATCAAATTCTTGCTATCAATGGACAGGCTCTTGATCAGACAATTACACATCAGCAGGCTATCAGCATCCTGCAG
AAAGCCAAAGATACTGTCCAGCTAGTTATTGCCAGAGGCTCATTGCCTCAGCTTGTCAGCCCCATAGTTTCCCGTTCTCCATCTGCAGCCAGCACAATTTCAGCT
CACTCTAATCCGGTTCACTGGCAACACATGGAAACGATTGAATTGGTGAATGATGGATCTGGTTTGGGATTTGGCATCATAGGAGGAAAAGCAACTGGTGTGATA
GTAAAAACCATTCTGCCTGGAGGAGTAGCTGATCAGCATGGGCGTTTATGCAGTGGAGACCACATTCTAAAGATTGGTGACACAGATCTAGCAGGAATGAGCAGT
GAGCAAGTAGCACAAGTCCTTAGGCAATGTGGAAATAGAGTTAAGTTGATGATTGCAAGAGGTGCCATAGAAGAACGTACAGCACCCACTGCTTTGGGCATCACC
CTCTCCTCATCCCCAACTTCAACACCAGAGTTGCGGGTTGATGCTTCTACTCAGAAAGGTGAAGAAAGTGAGACATTTGATGTAGAACTCACTAAAAATGTCCAA
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>MPDZ|8777|protein
MLEAIDKNRALHAAERLQTKLRERGDVANEDKLSLLKSVLQSPLFSQILSLQTSVQQLKDQVNIATSATSNIEYAHVPHLSPAVIPTLQNESFLLSPNNGNLEAL
TGPGIPHINGKPACDEFDQLIKNMAQGRHVEVFELLKPPSGGLGFSVVGLRSENRGELGIFVQEIQEGSVAHRDGRLKETDQILAINGQALDQTITHQQAISILQ
KAKDTVQLVIARGSLPQLVSPIVSRSPSAASTISAHSNPVHWQHMETIELVNDGSGLGFGIIGGKATGVIVKTILPGGVADQHGRLCSGDHILKIGDTDLAGMSS
EQVAQVLRQCGNRVKLMIARGAIEERTAPTALGITLSSSPTSTPELRVDASTQKGEESETFDVELTKNVQGLGITIAGYIGDKKLEPSGIFVKSITKSSAVEHDG
RIQIGDQIIAVDGTNLQGFTNQQAVEVLRHTGQTVLLTLMRRGMKQEAELMSREDVTKDADLSPVNASIIKENYEKDEDFLSSTRNTNILPTEEEGYPLLSAEIE
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MLEAIDKNRALHAAERLQTKLRERGDVANEDKLSLLKSVLQSPLFSQILSLQTSVQQLKDQVNIATSATSNIEYAHVPHLSPAVIPTLQNESFLLSPNNGNLEAL
TGPGIPHINGKPACDEFDQLIKNMAQGRHVEVFELLKPPSGGLGFSVVGLRSENRGELGIFVQEIQEGSVAHRDGRLKETDQILAINGQALDQTITHQQAISILQ
KAKDTVQLVIARGSLPQLVSPIVSRSPSAASTISAHSNPVHWQHMETIELVNDGSGLGFGIIGGKATGVIVKTILPGGVADQHGRLCSGDHILKIGDTDLAGMSS
EQVAQVLRQCGNRVKLMIARGAIEERTAPTALGITLSSSPTSTPELRVDASTQKGEESETFDVELTKNVQGLGITIAGYIGDKKLEPSGIFVKSITKSSAVEHDG
RIQIGDQIIAVDGTNLQGFTNQQAVEVLRHTGQTVLLTLMRRGMKQEAELMSREDVTKDADLSPVNASIIKENYEKDEDFLSSTRNTNILPTEEEGYPLLSAEIE
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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 (2) | 0 (0) | 0 (0) | 0 (0) | 2 (3) | 0 (0) | 0 (0) | 0 (0) | 22 (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 | ||||||
Szatmari, 2007 | Europe, North America | SNP microarray | ASD | 1491 | - | - | - | - | - | 0 | ||
Bucan, 2009 | USA | SNP microarray | autism, ASD | 912 | - | 912 | - | - | 1488 | 1488 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Neale BM, 2012 | 175 | 175 | 173 | Patterns and rates of exonic de novo mutations in autism spectrum disorders. |
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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