Evidence Details for ZC3H11A


Gene Symbol: | ZC3H11A ( DKFZp686D03108,DKFZp686F14109,DKFZp781G2455,KIAA0663,ZC3HDC11A ) |
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Gene Full Name: | zinc finger CCCH-type containing 11A |
Band: | 1q32.1 |
Quick Links | Entrez ID:9877; OMIM: 613513; Uniprot ID:ZC11A_HUMAN; ENSEMBL ID: ENSG00000058673; HGNC ID: 29093 |
Relate to Another Database: | SFARIGene; denovo-db |


>ZC3H11A|9877|nucleotide
ATGCCTAATCAAGGAGAAGACTGCTATTTTTTTTTCTATTCCACATGTACCAAAGGCGACAGCTGCCCATTCCGTCACTGTGAAGCTGCAATAGGAAATGAAACT
GTTTGCACATTATGGCAAGAAGGGCGCTGTTTTCGACAGGTGTGCAGGTTTCGGCACATGGAGATTGATAAAAAACGCAGTGAAATTCCTTGTTATTGGGAAAAT
CAGCCAACAGGATGTCAAAAATTAAACTGCGCTTTCCATCACAATAGAGGACGATATGTTGATGGCCTTTTCCTACCTCCGAGCAAAACTGTGTTGCCCACTGTG
CCTGAGTCACCAGAAGAGGAAGTGAAGGCTAGCCAACTTTCAGTTCAGCAGAACAAATTGTCTGTCCAGTCCAATCCTTCCCCTCAGCTGCGGAGCGTTATGAAA
GTAGAAAGTTCCGAAAATGTTCCTAGCCCCACGCATCCACCAGTTGTAATTAATGCTGCAGATGATGATGAAGATGATGATGATCAGTTTTCTGAGGAAGGTGAT
GAAACCAAAACACCTACCCTGCAACCAACTCCTGAAGTTCACAATGGATTACGAGTGACTTCTGTCCGGAAACCTGCAGTCAATATAAAGCAAGGTGAATGTTTG
AATTTTGGAATAAAAACTCTTGAGGAAATTAAGTCAAAGAAAATGAAGGAAAAATCTAAGAAGCAAGGTGAGGGTTCTTCAGGAGTTTCCAGTCTTTTACTCCAC
CCTGAGCCCGTTCCAGGTCCTGAAAAAGAAAATGTCAGGACTGTGGTGAGGACAGTAACTCTCTCCACCAAACAAGGAGAAGAACCCTTGGTTAGATTGAGTCTT
ACTGAGAGACTGGGGAAACGAAAATTTTCAGCAGGCGGTGACAGTGATCCTCCATTAAAGCGTAGCCTGGCACAGAGGCTAGGGAAGAAAGTTGAAGCTCCAGAA
ACTAACATTGACAAAACACCAAAGAAAGCTCAAGTTTCCAAGTCTCTTAAGGAGCGATTAGGCATGTCAGCTGATCCAGATAATGAGGATGCAACAGATAAAGTT
AATAAAGTTGGTGAGATCCATGTGAAGACATTAGAAGAAATTCTTCTTGAAAGAGCCAGTCAGAAACGTGGAGAATTGCAAACTAAACTCAAGACAGAAGGACCT
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ATGCCTAATCAAGGAGAAGACTGCTATTTTTTTTTCTATTCCACATGTACCAAAGGCGACAGCTGCCCATTCCGTCACTGTGAAGCTGCAATAGGAAATGAAACT
GTTTGCACATTATGGCAAGAAGGGCGCTGTTTTCGACAGGTGTGCAGGTTTCGGCACATGGAGATTGATAAAAAACGCAGTGAAATTCCTTGTTATTGGGAAAAT
CAGCCAACAGGATGTCAAAAATTAAACTGCGCTTTCCATCACAATAGAGGACGATATGTTGATGGCCTTTTCCTACCTCCGAGCAAAACTGTGTTGCCCACTGTG
CCTGAGTCACCAGAAGAGGAAGTGAAGGCTAGCCAACTTTCAGTTCAGCAGAACAAATTGTCTGTCCAGTCCAATCCTTCCCCTCAGCTGCGGAGCGTTATGAAA
GTAGAAAGTTCCGAAAATGTTCCTAGCCCCACGCATCCACCAGTTGTAATTAATGCTGCAGATGATGATGAAGATGATGATGATCAGTTTTCTGAGGAAGGTGAT
GAAACCAAAACACCTACCCTGCAACCAACTCCTGAAGTTCACAATGGATTACGAGTGACTTCTGTCCGGAAACCTGCAGTCAATATAAAGCAAGGTGAATGTTTG
AATTTTGGAATAAAAACTCTTGAGGAAATTAAGTCAAAGAAAATGAAGGAAAAATCTAAGAAGCAAGGTGAGGGTTCTTCAGGAGTTTCCAGTCTTTTACTCCAC
CCTGAGCCCGTTCCAGGTCCTGAAAAAGAAAATGTCAGGACTGTGGTGAGGACAGTAACTCTCTCCACCAAACAAGGAGAAGAACCCTTGGTTAGATTGAGTCTT
ACTGAGAGACTGGGGAAACGAAAATTTTCAGCAGGCGGTGACAGTGATCCTCCATTAAAGCGTAGCCTGGCACAGAGGCTAGGGAAGAAAGTTGAAGCTCCAGAA
ACTAACATTGACAAAACACCAAAGAAAGCTCAAGTTTCCAAGTCTCTTAAGGAGCGATTAGGCATGTCAGCTGATCCAGATAATGAGGATGCAACAGATAAAGTT
AATAAAGTTGGTGAGATCCATGTGAAGACATTAGAAGAAATTCTTCTTGAAAGAGCCAGTCAGAAACGTGGAGAATTGCAAACTAAACTCAAGACAGAAGGACCT
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>ZC3H11A|9877|protein
MPNQGEDCYFFFYSTCTKGDSCPFRHCEAAIGNETVCTLWQEGRCFRQVCRFRHMEIDKKRSEIPCYWENQPTGCQKLNCAFHHNRGRYVDGLFLPPSKTVLPTV
PESPEEEVKASQLSVQQNKLSVQSNPSPQLRSVMKVESSENVPSPTHPPVVINAADDDEDDDDQFSEEGDETKTPTLQPTPEVHNGLRVTSVRKPAVNIKQGECL
NFGIKTLEEIKSKKMKEKSKKQGEGSSGVSSLLLHPEPVPGPEKENVRTVVRTVTLSTKQGEEPLVRLSLTERLGKRKFSAGGDSDPPLKRSLAQRLGKKVEAPE
TNIDKTPKKAQVSKSLKERLGMSADPDNEDATDKVNKVGEIHVKTLEEILLERASQKRGELQTKLKTEGPSKTDDSTSGARSSSTIRIKTFSEVLAEKKHRQQEA
ERQKSKKDTTCIKLKIDSEIKKTVVLPPIVASRGQSEEPAGKTKSMQEVHIKTLEEIKLEKALRVQQSSESSTSSPSQHEATPGARRLLRITKRTGMKEEKNLQE
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MPNQGEDCYFFFYSTCTKGDSCPFRHCEAAIGNETVCTLWQEGRCFRQVCRFRHMEIDKKRSEIPCYWENQPTGCQKLNCAFHHNRGRYVDGLFLPPSKTVLPTV
PESPEEEVKASQLSVQQNKLSVQSNPSPQLRSVMKVESSENVPSPTHPPVVINAADDDEDDDDQFSEEGDETKTPTLQPTPEVHNGLRVTSVRKPAVNIKQGECL
NFGIKTLEEIKSKKMKEKSKKQGEGSSGVSSLLLHPEPVPGPEKENVRTVVRTVTLSTKQGEEPLVRLSLTERLGKRKFSAGGDSDPPLKRSLAQRLGKKVEAPE
TNIDKTPKKAQVSKSLKERLGMSADPDNEDATDKVNKVGEIHVKTLEEILLERASQKRGELQTKLKTEGPSKTDDSTSGARSSSTIRIKTFSEVLAEKKHRQQEA
ERQKSKKDTTCIKLKIDSEIKKTVVLPPIVASRGQSEEPAGKTKSMQEVHIKTLEEIKLEKALRVQQSSESSTSSPSQHEATPGARRLLRITKRTGMKEEKNLQE
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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 |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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