Evidence Details for C11orf24
Basic Information Top
Gene Symbol: | C11orf24 ( DM4E3 ) |
---|---|
Gene Full Name: | chromosome 11 open reading frame 24 |
Band: | 11q13.2 |
Quick Links | Entrez ID:53838; OMIM: 610880; Uniprot ID:CK024_HUMAN; ENSEMBL ID: ENSG00000171067; HGNC ID: 1174 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C11orf24|53838|nucleotide
ATGTGGACAGCTCTTGTGCTCATTTGGATTTTCTCCTTGTCCTTATCTGAAAGCCATGCGGCATCCAACGATCCACGCAACTTTGTCCCTAACAAAATGTGGAAG
GGATTAGTCAAGAGGAATGCATCTGTGGAAACAGTTGATAATAAAACGTCTGAGGATGTAACCATGGCAGCAGCTTCTCCTGTCACATTGACCAAAGGGACTTCG
GCAGCCCACCTCAACTCTATGGAAGTCACAACAGAGGACACAAGCAGGACAGATGTGAGTGAACCAGCAACTTCAGGAGGTGCAGCTGATGGTGTGACCTCCATT
GCTCCCACGGCTGTGGCCTCCAGTACGACTGCGGCCTCCATTACGACTGCGGCCTCCAGTATGACTGTGGCCTCCAGTGCTCCCACGACTGCAGCCTCCAGTACA
ACTGTGGCCTCCATTGCTCCCACGACTGCAGCCTCCAGTATGACTGCGGCCTCCAGCACTCCCATGACACTTGCACTCCCCGCGCCCACGTCCACTTCCACAGGG
CGGACCCCGTCCACTACCGCCACTGGGCATCCATCTCTCAGCACAGCCCTCGCACAAGTGCCAAAGAGCAGCGCGTTGCCAAGAACAGCAACCCTGGCCACATTG
GCCACACGTGCTCAGACTGTAGCGACCACAGCAAACACAAGCAGCCCCATGAGCACTCGTCCAAGTCCTTCCAAGCACATGCCCAGTGACACCGCGGCAAGCCCT
GTACCCCCTATGCGTCCCCAAGCACAAGGTCCCATTAGCCAGGTGTCAGTGGACCAGCCTGTGGTTAACACAACAAATAAATCCACACCCATGCCCTCAAACACA
ACCCCAGAGCCCGCCCCCACCCCCACAGTGGTGACCACCACCAAGGCACAAGCCAGGGAGCCAACTGCCAGCCCAGTGCCAGTACCTCACACCAGCCCAATCCCT
GAGATGGAGGCCATGTCCCCCACGACACAGCCAAGCCCCATGCCATATACCCAGAGGGCCGCTGGGCCAGGCACATCCCAGGCACCGGAGCAGGTAGAGACTGAA
GCCACACCAGGTACTGATTCCACTGGGCCAACACCCAGGAGCTCAGGGGGCACTAAGATGCCAGCCACGGACTCGTGCCAGCCCAGCACCCAAGGCCAGTACATG
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ATGTGGACAGCTCTTGTGCTCATTTGGATTTTCTCCTTGTCCTTATCTGAAAGCCATGCGGCATCCAACGATCCACGCAACTTTGTCCCTAACAAAATGTGGAAG
GGATTAGTCAAGAGGAATGCATCTGTGGAAACAGTTGATAATAAAACGTCTGAGGATGTAACCATGGCAGCAGCTTCTCCTGTCACATTGACCAAAGGGACTTCG
GCAGCCCACCTCAACTCTATGGAAGTCACAACAGAGGACACAAGCAGGACAGATGTGAGTGAACCAGCAACTTCAGGAGGTGCAGCTGATGGTGTGACCTCCATT
GCTCCCACGGCTGTGGCCTCCAGTACGACTGCGGCCTCCATTACGACTGCGGCCTCCAGTATGACTGTGGCCTCCAGTGCTCCCACGACTGCAGCCTCCAGTACA
ACTGTGGCCTCCATTGCTCCCACGACTGCAGCCTCCAGTATGACTGCGGCCTCCAGCACTCCCATGACACTTGCACTCCCCGCGCCCACGTCCACTTCCACAGGG
CGGACCCCGTCCACTACCGCCACTGGGCATCCATCTCTCAGCACAGCCCTCGCACAAGTGCCAAAGAGCAGCGCGTTGCCAAGAACAGCAACCCTGGCCACATTG
GCCACACGTGCTCAGACTGTAGCGACCACAGCAAACACAAGCAGCCCCATGAGCACTCGTCCAAGTCCTTCCAAGCACATGCCCAGTGACACCGCGGCAAGCCCT
GTACCCCCTATGCGTCCCCAAGCACAAGGTCCCATTAGCCAGGTGTCAGTGGACCAGCCTGTGGTTAACACAACAAATAAATCCACACCCATGCCCTCAAACACA
ACCCCAGAGCCCGCCCCCACCCCCACAGTGGTGACCACCACCAAGGCACAAGCCAGGGAGCCAACTGCCAGCCCAGTGCCAGTACCTCACACCAGCCCAATCCCT
GAGATGGAGGCCATGTCCCCCACGACACAGCCAAGCCCCATGCCATATACCCAGAGGGCCGCTGGGCCAGGCACATCCCAGGCACCGGAGCAGGTAGAGACTGAA
GCCACACCAGGTACTGATTCCACTGGGCCAACACCCAGGAGCTCAGGGGGCACTAAGATGCCAGCCACGGACTCGTGCCAGCCCAGCACCCAAGGCCAGTACATG
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>C11orf24|53838|protein
MWTALVLIWIFSLSLSESHAASNDPRNFVPNKMWKGLVKRNASVETVDNKTSEDVTMAAASPVTLTKGTSAAHLNSMEVTTEDTSRTDVSEPATSGGAADGVTSI
APTAVASSTTAASITTAASSMTVASSAPTTAASSTTVASIAPTTAASSMTAASSTPMTLALPAPTSTSTGRTPSTTATGHPSLSTALAQVPKSSALPRTATLATL
ATRAQTVATTANTSSPMSTRPSPSKHMPSDTAASPVPPMRPQAQGPISQVSVDQPVVNTTNKSTPMPSNTTPEPAPTPTVVTTTKAQAREPTASPVPVPHTSPIP
EMEAMSPTTQPSPMPYTQRAAGPGTSQAPEQVETEATPGTDSTGPTPRSSGGTKMPATDSCQPSTQGQYMVVTTEPLTQAVVDKTLLLVVLLLGVTLFITVLVLF
ALQAYESYKKKDYTQVDYLINGMYADSEM
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MWTALVLIWIFSLSLSESHAASNDPRNFVPNKMWKGLVKRNASVETVDNKTSEDVTMAAASPVTLTKGTSAAHLNSMEVTTEDTSRTDVSEPATSGGAADGVTSI
APTAVASSTTAASITTAASSMTVASSAPTTAASSTTVASIAPTTAASSMTAASSTPMTLALPAPTSTSTGRTPSTTATGHPSLSTALAQVPKSSALPRTATLATL
ATRAQTVATTANTSSPMSTRPSPSKHMPSDTAASPVPPMRPQAQGPISQVSVDQPVVNTTNKSTPMPSNTTPEPAPTPTVVTTTKAQAREPTASPVPVPHTSPIP
EMEAMSPTTQPSPMPYTQRAAGPGTSQAPEQVETEATPGTDSTGPTPRSSGGTKMPATDSCQPSTQGQYMVVTTEPLTQAVVDKTLLLVVLLLGVTLFITVLVLF
ALQAYESYKKKDYTQVDYLINGMYADSEM
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
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 |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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