Evidence Details for MPP6


Gene Symbol: | MPP6 ( PALS2,VAM-1,VAM1,p55T ) |
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Gene Full Name: | membrane protein, palmitoylated 6 (MAGUK p55 subfamily member 6) |
Band: | 7p15.3 |
Quick Links | Entrez ID:51678; OMIM: 606959; Uniprot ID:MPP6_HUMAN; ENSEMBL ID: ENSG00000105926; HGNC ID: 18167 |
Relate to Another Database: | SFARIGene; denovo-db |


>MPP6|51678|nucleotide
ATGCAGCAAGTCTTGGAAAACCTTACGGAGCTGCCCTCGTCTACTGGAGCAGAAGAAATAGACCTAATTTTCCTCAAGGGAATTATGGAGAATCCTATTGTAAAA
TCACTTGCTAAGGCTCATGAGAGGCTAGAAGATTCCAAACTAGAAGCTGTCAGTGACAATAACTTGGAATTAGTCAATGAAATTCTTGAAGACATCACTCCTCTA
ATAAATGTGGATGAAAATGTGGCAGAATTGGTTGGTATACTCAAAGAACCTCACTTCCAGTCACTGTTGGAGGCCCATGATATTGTGGCATCAAAGTGTTATGAT
TCACCTCCATCAAGCCCAGAAATGAATAATTCTTCTATCAATAATCAGTTATTACCAGTAGATGCCATTCGTATTCTTGGTATTCACAAAAGAGCTGGGGAACCA
CTGGGTGTGACATTTAGGGTTGAAAATAATGATCTGGTAATTGCCCGAATCCTCCATGGGGGAATGATAGATCGACAAGGTCTACTTCATGTGGGAGATATAATT
AAAGAAGTCAATGGCCATGAGGTTGGAAATAATCCAAAGGAATTACAAGAATTACTGAAAAATATTAGTGGAAGTGTCACCCTAAAAATCTTACCAAGTTATAGA
GATACCATTACTCCTCAACAGGTATTTGTGAAGTGTCATTTTGATTATAATCCATACAATGACAACCTAATACCTTGCAAAGAAGCAGGATTGAAGTTTTCCAAA
GGAGAAATTCTTCAGATTGTAAATAGAGAAGATCCAAATTGGTGGCAGGCTAGCCATGTAAAAGAGGGAGGAAGCGCTGGTCTCATTCCAAGCCAGTTCCTGGAA
GAGAAGAGAAAGGCATTTGTTAGAAGAGACTGGGACAATTCAGGACCTTTTTGTGGAACTATAAGTAGCAAAAAAAAGAAAAAGATGATGTATCTCACAACCAGA
AATGCAGAATTTGATCGTCATGAAATCCAGATATATGAGGAGGTAGCCAAAATGCCTCCCTTCCAGAGAAAAACATTAGTATTGATAGGAGCTCAAGGTGTAGGC
CGAAGAAGCTTGAAAAACAGGTTCATAGTATTGAATCCCACTAGATTTGGAACTACGGTGCCATTTACTTCACGGAAACCAAGGGAAGATGAAAAAGATGGCCAG
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ATGCAGCAAGTCTTGGAAAACCTTACGGAGCTGCCCTCGTCTACTGGAGCAGAAGAAATAGACCTAATTTTCCTCAAGGGAATTATGGAGAATCCTATTGTAAAA
TCACTTGCTAAGGCTCATGAGAGGCTAGAAGATTCCAAACTAGAAGCTGTCAGTGACAATAACTTGGAATTAGTCAATGAAATTCTTGAAGACATCACTCCTCTA
ATAAATGTGGATGAAAATGTGGCAGAATTGGTTGGTATACTCAAAGAACCTCACTTCCAGTCACTGTTGGAGGCCCATGATATTGTGGCATCAAAGTGTTATGAT
TCACCTCCATCAAGCCCAGAAATGAATAATTCTTCTATCAATAATCAGTTATTACCAGTAGATGCCATTCGTATTCTTGGTATTCACAAAAGAGCTGGGGAACCA
CTGGGTGTGACATTTAGGGTTGAAAATAATGATCTGGTAATTGCCCGAATCCTCCATGGGGGAATGATAGATCGACAAGGTCTACTTCATGTGGGAGATATAATT
AAAGAAGTCAATGGCCATGAGGTTGGAAATAATCCAAAGGAATTACAAGAATTACTGAAAAATATTAGTGGAAGTGTCACCCTAAAAATCTTACCAAGTTATAGA
GATACCATTACTCCTCAACAGGTATTTGTGAAGTGTCATTTTGATTATAATCCATACAATGACAACCTAATACCTTGCAAAGAAGCAGGATTGAAGTTTTCCAAA
GGAGAAATTCTTCAGATTGTAAATAGAGAAGATCCAAATTGGTGGCAGGCTAGCCATGTAAAAGAGGGAGGAAGCGCTGGTCTCATTCCAAGCCAGTTCCTGGAA
GAGAAGAGAAAGGCATTTGTTAGAAGAGACTGGGACAATTCAGGACCTTTTTGTGGAACTATAAGTAGCAAAAAAAAGAAAAAGATGATGTATCTCACAACCAGA
AATGCAGAATTTGATCGTCATGAAATCCAGATATATGAGGAGGTAGCCAAAATGCCTCCCTTCCAGAGAAAAACATTAGTATTGATAGGAGCTCAAGGTGTAGGC
CGAAGAAGCTTGAAAAACAGGTTCATAGTATTGAATCCCACTAGATTTGGAACTACGGTGCCATTTACTTCACGGAAACCAAGGGAAGATGAAAAAGATGGCCAG
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>MPP6|51678|protein
MQQVLENLTELPSSTGAEEIDLIFLKGIMENPIVKSLAKAHERLEDSKLEAVSDNNLELVNEILEDITPLINVDENVAELVGILKEPHFQSLLEAHDIVASKCYD
SPPSSPEMNNSSINNQLLPVDAIRILGIHKRAGEPLGVTFRVENNDLVIARILHGGMIDRQGLLHVGDIIKEVNGHEVGNNPKELQELLKNISGSVTLKILPSYR
DTITPQQVFVKCHFDYNPYNDNLIPCKEAGLKFSKGEILQIVNREDPNWWQASHVKEGGSAGLIPSQFLEEKRKAFVRRDWDNSGPFCGTISSKKKKKMMYLTTR
NAEFDRHEIQIYEEVAKMPPFQRKTLVLIGAQGVGRRSLKNRFIVLNPTRFGTTVPFTSRKPREDEKDGQAYKFVSRSEMEADIKAGKYLEHGEYEGNLYGTKID
SILEVVQTGRTCILDVNPQALKVLRTSEFMPYVVFIAAPELETLRAMHKAVVDAGITTKLLTDSDLKKTVDESARIQRAYNHYFDLIIINDNLDKAFEKLQTAIE
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MQQVLENLTELPSSTGAEEIDLIFLKGIMENPIVKSLAKAHERLEDSKLEAVSDNNLELVNEILEDITPLINVDENVAELVGILKEPHFQSLLEAHDIVASKCYD
SPPSSPEMNNSSINNQLLPVDAIRILGIHKRAGEPLGVTFRVENNDLVIARILHGGMIDRQGLLHVGDIIKEVNGHEVGNNPKELQELLKNISGSVTLKILPSYR
DTITPQQVFVKCHFDYNPYNDNLIPCKEAGLKFSKGEILQIVNREDPNWWQASHVKEGGSAGLIPSQFLEEKRKAFVRRDWDNSGPFCGTISSKKKKKMMYLTTR
NAEFDRHEIQIYEEVAKMPPFQRKTLVLIGAQGVGRRSLKNRFIVLNPTRFGTTVPFTSRKPREDEKDGQAYKFVSRSEMEADIKAGKYLEHGEYEGNLYGTKID
SILEVVQTGRTCILDVNPQALKVLRTSEFMPYVVFIAAPELETLRAMHKAVVDAGITTKLLTDSDLKKTVDESARIQRAYNHYFDLIIINDNLDKAFEKLQTAIE
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |














Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Sanders SJ, 2012 | - | 238 | 172 | De novo mutations revealed by whole-exome sequencing are strongly associated with autism. |






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