Evidence Details for DDX24
Basic Information Top
Gene Symbol: | DDX24 ( - ) |
---|---|
Gene Full Name: | DEAD (Asp-Glu-Ala-Asp) box polypeptide 24 |
Band: | 14q32.12 |
Quick Links | Entrez ID:57062; OMIM: 606181; Uniprot ID:DDX24_HUMAN; ENSEMBL ID: ENSG00000089737; HGNC ID: 13266 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>DDX24|57062|nucleotide
ATGAAGTTGAAGGACACAAAATCAAGGCCAAAGCAGTCAAGCTGTGGCAAATTTCAGACAAAGGGAATCAAAGTTGTGGGAAAATGGAAGGAAGTGAAGATTGAC
CCAAATATGTTTGCAGATGGACAGATGGATGACTTGGTGTGCTTTGAGGAATTGACAGATTACCAGTTGGTCTCCCCTGCCAAGAATCCCTCCAGTCTCTTCTCA
AAGGAAGCACCCAAGAGAAAGGCACAAGCTGTTTCAGAAGAAGAGGAGGAGGAGGAGGGAAAGTCTAGCTCACCAAAGAAAAAGATCAAGTTGAAGAAAAGTAAA
AATGTAGCAACTGAAGGAACCAGTACCCAGAAAGAATTTGAAGTGAAAGATCCTGAGCTGGAGGCCCAGGGAGATGACATGGTTTGTGATGATCCGGAGGCTGGG
GAGATGACATCAGAAAACCTGGTCCAAACTGCTCCAAAAAAGAAGAAAAATAAAGGGAAAAAAGGGTTGGAGCCTTCTCAGAGCACTGCTGCCAAGGTGCCCAAA
AAAGCGAAGACATGGATTCCTGAAGTTCATGATCAGAAAGCAGATGTGTCAGCTTGGAAGGACCTGTTTGTTCCCAGGCCGGTTCTCCGAGCACTCAGCTTTCTA
GGCTTCTCTGCACCCACACCAATCCAAGCCCTGACCTTGGCACCTGCCATCCGTGACAAACTGGACATCCTTGGGGCTGCTGAGACAGGAAGTGGGAAAACTCTT
GCCTTTGCCATCCCAATGATTCATGCGGTGTTGCAGTGGCAGAAGAGGAATGCTGCCCCTCCTCCAAGTAACACCGAAGCACCACCTGGAGAGACCAGAACTGAG
GCCGGAGCTGAGACTAGATCACCAGGCAAGGCTGAAGCTGAGTCTGATGCATTGCCTGACGATACTGTAATTGAGAGTGAAGCACTGCCCAGTGATATTGCAGCC
GAGGCCAGAGCCAAGACTGGAGGCACTGTCTCAGACCAGGCGTTGCTCTTTGGTGACGATGATGCTGGTGAAGGGCCTTCTTCCCTGATCAGGGAGAAACCTGTT
CCCAAACAGAATGAGAATGAGGAGGAAAATCTTGATAAAGAGCAGACTGGAAATCTAAAACAGGAGTTGGATGACAAAAGCGCCACCTGTAAGGCATATCCAAAG
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ATGAAGTTGAAGGACACAAAATCAAGGCCAAAGCAGTCAAGCTGTGGCAAATTTCAGACAAAGGGAATCAAAGTTGTGGGAAAATGGAAGGAAGTGAAGATTGAC
CCAAATATGTTTGCAGATGGACAGATGGATGACTTGGTGTGCTTTGAGGAATTGACAGATTACCAGTTGGTCTCCCCTGCCAAGAATCCCTCCAGTCTCTTCTCA
AAGGAAGCACCCAAGAGAAAGGCACAAGCTGTTTCAGAAGAAGAGGAGGAGGAGGAGGGAAAGTCTAGCTCACCAAAGAAAAAGATCAAGTTGAAGAAAAGTAAA
AATGTAGCAACTGAAGGAACCAGTACCCAGAAAGAATTTGAAGTGAAAGATCCTGAGCTGGAGGCCCAGGGAGATGACATGGTTTGTGATGATCCGGAGGCTGGG
GAGATGACATCAGAAAACCTGGTCCAAACTGCTCCAAAAAAGAAGAAAAATAAAGGGAAAAAAGGGTTGGAGCCTTCTCAGAGCACTGCTGCCAAGGTGCCCAAA
AAAGCGAAGACATGGATTCCTGAAGTTCATGATCAGAAAGCAGATGTGTCAGCTTGGAAGGACCTGTTTGTTCCCAGGCCGGTTCTCCGAGCACTCAGCTTTCTA
GGCTTCTCTGCACCCACACCAATCCAAGCCCTGACCTTGGCACCTGCCATCCGTGACAAACTGGACATCCTTGGGGCTGCTGAGACAGGAAGTGGGAAAACTCTT
GCCTTTGCCATCCCAATGATTCATGCGGTGTTGCAGTGGCAGAAGAGGAATGCTGCCCCTCCTCCAAGTAACACCGAAGCACCACCTGGAGAGACCAGAACTGAG
GCCGGAGCTGAGACTAGATCACCAGGCAAGGCTGAAGCTGAGTCTGATGCATTGCCTGACGATACTGTAATTGAGAGTGAAGCACTGCCCAGTGATATTGCAGCC
GAGGCCAGAGCCAAGACTGGAGGCACTGTCTCAGACCAGGCGTTGCTCTTTGGTGACGATGATGCTGGTGAAGGGCCTTCTTCCCTGATCAGGGAGAAACCTGTT
CCCAAACAGAATGAGAATGAGGAGGAAAATCTTGATAAAGAGCAGACTGGAAATCTAAAACAGGAGTTGGATGACAAAAGCGCCACCTGTAAGGCATATCCAAAG
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>DDX24|57062|protein
MKLKDTKSRPKQSSCGKFQTKGIKVVGKWKEVKIDPNMFADGQMDDLVCFEELTDYQLVSPAKNPSSLFSKEAPKRKAQAVSEEEEEEEGKSSSPKKKIKLKKSK
NVATEGTSTQKEFEVKDPELEAQGDDMVCDDPEAGEMTSENLVQTAPKKKKNKGKKGLEPSQSTAAKVPKKAKTWIPEVHDQKADVSAWKDLFVPRPVLRALSFL
GFSAPTPIQALTLAPAIRDKLDILGAAETGSGKTLAFAIPMIHAVLQWQKRNAAPPPSNTEAPPGETRTEAGAETRSPGKAEAESDALPDDTVIESEALPSDIAA
EARAKTGGTVSDQALLFGDDDAGEGPSSLIREKPVPKQNENEEENLDKEQTGNLKQELDDKSATCKAYPKRPLLGLVLTPTRELAVQVKQHIDAVARFTGIKTAI
LVGGMSTQKQQRMLNRRPEIVVATPGRLWELIKEKHYHLRNLRQLRCLVVDEADRMVEKGHFAELSQLLEMLNDSQYNPKRQTLVFSATLTLVHQAPARILHKKH
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MKLKDTKSRPKQSSCGKFQTKGIKVVGKWKEVKIDPNMFADGQMDDLVCFEELTDYQLVSPAKNPSSLFSKEAPKRKAQAVSEEEEEEEGKSSSPKKKIKLKKSK
NVATEGTSTQKEFEVKDPELEAQGDDMVCDDPEAGEMTSENLVQTAPKKKKNKGKKGLEPSQSTAAKVPKKAKTWIPEVHDQKADVSAWKDLFVPRPVLRALSFL
GFSAPTPIQALTLAPAIRDKLDILGAAETGSGKTLAFAIPMIHAVLQWQKRNAAPPPSNTEAPPGETRTEAGAETRSPGKAEAESDALPDDTVIESEALPSDIAA
EARAKTGGTVSDQALLFGDDDAGEGPSSLIREKPVPKQNENEEENLDKEQTGNLKQELDDKSATCKAYPKRPLLGLVLTPTRELAVQVKQHIDAVARFTGIKTAI
LVGGMSTQKQQRMLNRRPEIVVATPGRLWELIKEKHYHLRNLRQLRCLVVDEADRMVEKGHFAELSQLLEMLNDSQYNPKRQTLVFSATLTLVHQAPARILHKKH
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Evidence summary Top
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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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