Evidence Details for C11orf42


Gene Symbol: | C11orf42 ( MGC34805 ) |
---|---|
Gene Full Name: | chromosome 11 open reading frame 42 |
Band: | 11p15.4 |
Quick Links | Entrez ID:160298; OMIM: NA; Uniprot ID:CK042_HUMAN; ENSEMBL ID: ENSG00000180878; HGNC ID: 28541 |
Relate to Another Database: | SFARIGene; denovo-db |


>C11orf42|160298|nucleotide
ATGTTGGTGGGTACCCCCAACCTGCTGACACTGGATGAAGCTGATGCCACCTGGACCCTCATCAAGGATAAGGTCATCGAGGAGCACTTTGGGCCCAATGCAGTA
GCAGTACCTTTCCTGTCAGATGCAGCCTGCTATGACCTACTGGGTGTGCTGGTAAAACAGTCCCGCCCAGCCCATACCCGCCTGGCTTTGCCAGGTCGGCAGGGC
CGGAGGGCACTGAAACCAGTGGGGCCACTACCAAGCCTCCTGGAGCAGGCAGGATCTGAGGGTGCCTTCGCCCACTGCACTCGGGAATACTCACCAAATGGCCGA
GCAGAGAGAGCCTATGAAGAGACGCGAATGTTGGATGGACAGCCCTGCAAGATCCGCCTACATATGGGTGACCTGCGCAAGAAGGTTGCCTTCCTGTTGCTGCCA
CCAGGGCAGGTGAGCCTACAGCAGACTCTTCCCTGGCTCCGAAGCACCCACAGCATCTATGTCATCTACCAGGTCTTCTCTTGTTCCTGGCTGCAGCTGGGGCTG
ACGTCTACAGCCCGTGAGCCCCAGCTCCTCCGGCTACTTCGGTCATTACCTGTTGCCTTCTCCTGCCTCAAGTTTTCACTGCAGTCTAAGGGCGTGCTGGGACCA
CAGAAGCCTCTCACTAAAGACCCATTGCCCCATGGGGCCAACTGGGTCAGACCCAACCTCAGCATCATGCCGCCTCTGGCCCCCACATCAGCACCTGCTGATACA
ACTGAAGCTGCTGATGTGCCCCCACCTGTCCCAGCCCCACCTACGCCACCTCCCCAGGAAGGGCCAGAGGACAAACCCACCAGATTCTCCTACAAGGGCCGAAAC
CCCTTCTGGAGGGGGCCCCAGATACTGTCAGAGAACTGGCTCTTCAGCCCCCGCAGCCCTCCACCAGGAGCCCAGGGTGGGGGCCCCAGGGACCCCGACGGGCAC
TCCATGTCCCTGCCCCTGCTGCAGGGTCTATCCTCAGAGTTCGACAGTGACGACTGA
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ATGTTGGTGGGTACCCCCAACCTGCTGACACTGGATGAAGCTGATGCCACCTGGACCCTCATCAAGGATAAGGTCATCGAGGAGCACTTTGGGCCCAATGCAGTA
GCAGTACCTTTCCTGTCAGATGCAGCCTGCTATGACCTACTGGGTGTGCTGGTAAAACAGTCCCGCCCAGCCCATACCCGCCTGGCTTTGCCAGGTCGGCAGGGC
CGGAGGGCACTGAAACCAGTGGGGCCACTACCAAGCCTCCTGGAGCAGGCAGGATCTGAGGGTGCCTTCGCCCACTGCACTCGGGAATACTCACCAAATGGCCGA
GCAGAGAGAGCCTATGAAGAGACGCGAATGTTGGATGGACAGCCCTGCAAGATCCGCCTACATATGGGTGACCTGCGCAAGAAGGTTGCCTTCCTGTTGCTGCCA
CCAGGGCAGGTGAGCCTACAGCAGACTCTTCCCTGGCTCCGAAGCACCCACAGCATCTATGTCATCTACCAGGTCTTCTCTTGTTCCTGGCTGCAGCTGGGGCTG
ACGTCTACAGCCCGTGAGCCCCAGCTCCTCCGGCTACTTCGGTCATTACCTGTTGCCTTCTCCTGCCTCAAGTTTTCACTGCAGTCTAAGGGCGTGCTGGGACCA
CAGAAGCCTCTCACTAAAGACCCATTGCCCCATGGGGCCAACTGGGTCAGACCCAACCTCAGCATCATGCCGCCTCTGGCCCCCACATCAGCACCTGCTGATACA
ACTGAAGCTGCTGATGTGCCCCCACCTGTCCCAGCCCCACCTACGCCACCTCCCCAGGAAGGGCCAGAGGACAAACCCACCAGATTCTCCTACAAGGGCCGAAAC
CCCTTCTGGAGGGGGCCCCAGATACTGTCAGAGAACTGGCTCTTCAGCCCCCGCAGCCCTCCACCAGGAGCCCAGGGTGGGGGCCCCAGGGACCCCGACGGGCAC
TCCATGTCCCTGCCCCTGCTGCAGGGTCTATCCTCAGAGTTCGACAGTGACGACTGA
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>C11orf42|160298|protein
MLVGTPNLLTLDEADATWTLIKDKVIEEHFGPNAVAVPFLSDAACYDLLGVLVKQSRPAHTRLALPGRQGRRALKPVGPLPSLLEQAGSEGAFAHCTREYSPNGR
AERAYEETRMLDGQPCKIRLHMGDLRKKVAFLLLPPGQVSLQQTLPWLRSTHSIYVIYQVFSCSWLQLGLTSTAREPQLLRLLRSLPVAFSCLKFSLQSKGVLGP
QKPLTKDPLPHGANWVRPNLSIMPPLAPTSAPADTTEAADVPPPVPAPPTPPPQEGPEDKPTRFSYKGRNPFWRGPQILSENWLFSPRSPPPGAQGGGPRDPDGH
SMSLPLLQGLSSEFDSDD
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MLVGTPNLLTLDEADATWTLIKDKVIEEHFGPNAVAVPFLSDAACYDLLGVLVKQSRPAHTRLALPGRQGRRALKPVGPLPSLLEQAGSEGAFAHCTREYSPNGR
AERAYEETRMLDGQPCKIRLHMGDLRKKVAFLLLPPGQVSLQQTLPWLRSTHSIYVIYQVFSCSWLQLGLTSTAREPQLLRLLRSLPVAFSCLKFSLQSKGVLGP
QKPLTKDPLPHGANWVRPNLSIMPPLAPTSAPADTTEAADVPPPVPAPPTPPPQEGPEDKPTRFSYKGRNPFWRGPQILSENWLFSPRSPPPGAQGGGPRDPDGH
SMSLPLLQGLSSEFDSDD
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |














Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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