Evidence Details for DCAF4L2
Basic Information Top
Gene Symbol: | DCAF4L2 ( FLJ35775,MGC133227,WDR21C ) |
---|---|
Gene Full Name: | DDB1 and CUL4 associated factor 4-like 2 |
Band: | 8q21.3 |
Quick Links | Entrez ID:138009; OMIM: NA; Uniprot ID:DC4L2_HUMAN; ENSEMBL ID: ENSG00000176566; HGNC ID: 26657 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>DCAF4L2|138009|nucleotide
ATGGAGAGCAAAAGACCGCGACTGCTCGAGGAAGCAGACAAGCAGAAAAAGACAGTCAGAGTGGGACTCAATGCACCTTCCATGCTACGAAAGAACCAGCTAGGT
TTCCTCAGATTCGCCAACTATTGCCGTATAGCTCGCGAGCTGCGTGTAAGCTGCATGCAGAGGAAAAAGGTCCAGATTCATAGCTGGGATCCCTCCTCTTTGGCA
AGCGACCGATTTAACCGCATACTGGCGAATACCAACACTGACCAGCTCTTCACAGTGAACCAAGTCGAAGCTGGAGGCTCCAAGTACGGCATCATCACCATGCGA
GGCCTGACGACCCCTGAGCTCCGGGTATACCCGCACAAAACCCTCTACGTCCCTAATCGGAAGGTGAATTCTATGTGCTGGGCCTCACTGAATCACTTGGATTCC
CACCTTCTGCTGTGCTTCGTGGGACTTGCAGATACTCCAAGCTGTGCCGTGCTGCTCCCAGCGTCGCTGTTCATAGGTAGCTTCCCAGGAATGCGTCGGCCTGGC
ATGCTTTGCAGTTTCCAGATCCCTGATGCCTGGTCCTGTGCCTGGTCCCTGAGCATCCACGCGTATCACTCTTTCAGTACAGGCTTGTCTCAGCAGGTCCTGTTG
ACCAACGTGGTGACGGGACACCAGCAGTCATTTGGGACTAGCAGTGATGTCTTGGCCCAGCAGTTTGCAATCATGACTCCTTTGCTGTTTAATGGCTGTCGCTCT
GGGGAGATCTTTGGCATTGATCTGCGCTGTGGAAATCAAGGCAGCGGGTGGAAGGCCATTTGCCTGTCCCATGATTCAGCAGTGACTTCTCTGCAAATCCTCCAA
GATGGCCAATTCCTGGTGTCATCAGACATGACTGGAACTATCAAGCTGTGGGACTTGAGGGCCACTAAATGTGTAACACAGTACGAAGGTCATGTGAATAACTCC
GCCTACCTACCCGTGCATGTGAACGAAGAAGAAGGAGTCGTGGCGGCCGTGGGCCAGGACTGCTACACGAGAATCTGGAGCCTCCGTCATGGCCACCTGCTCACA
ACCATACCCTCCCCATACCCCGCCTCGGAGAACGACATTCCCAGTGTGGCCTTCTCTTCTCGCCTCGGGGGCTTCCGAGGAGCACCAGGGCTGCTCATGGCTGTC
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ATGGAGAGCAAAAGACCGCGACTGCTCGAGGAAGCAGACAAGCAGAAAAAGACAGTCAGAGTGGGACTCAATGCACCTTCCATGCTACGAAAGAACCAGCTAGGT
TTCCTCAGATTCGCCAACTATTGCCGTATAGCTCGCGAGCTGCGTGTAAGCTGCATGCAGAGGAAAAAGGTCCAGATTCATAGCTGGGATCCCTCCTCTTTGGCA
AGCGACCGATTTAACCGCATACTGGCGAATACCAACACTGACCAGCTCTTCACAGTGAACCAAGTCGAAGCTGGAGGCTCCAAGTACGGCATCATCACCATGCGA
GGCCTGACGACCCCTGAGCTCCGGGTATACCCGCACAAAACCCTCTACGTCCCTAATCGGAAGGTGAATTCTATGTGCTGGGCCTCACTGAATCACTTGGATTCC
CACCTTCTGCTGTGCTTCGTGGGACTTGCAGATACTCCAAGCTGTGCCGTGCTGCTCCCAGCGTCGCTGTTCATAGGTAGCTTCCCAGGAATGCGTCGGCCTGGC
ATGCTTTGCAGTTTCCAGATCCCTGATGCCTGGTCCTGTGCCTGGTCCCTGAGCATCCACGCGTATCACTCTTTCAGTACAGGCTTGTCTCAGCAGGTCCTGTTG
ACCAACGTGGTGACGGGACACCAGCAGTCATTTGGGACTAGCAGTGATGTCTTGGCCCAGCAGTTTGCAATCATGACTCCTTTGCTGTTTAATGGCTGTCGCTCT
GGGGAGATCTTTGGCATTGATCTGCGCTGTGGAAATCAAGGCAGCGGGTGGAAGGCCATTTGCCTGTCCCATGATTCAGCAGTGACTTCTCTGCAAATCCTCCAA
GATGGCCAATTCCTGGTGTCATCAGACATGACTGGAACTATCAAGCTGTGGGACTTGAGGGCCACTAAATGTGTAACACAGTACGAAGGTCATGTGAATAACTCC
GCCTACCTACCCGTGCATGTGAACGAAGAAGAAGGAGTCGTGGCGGCCGTGGGCCAGGACTGCTACACGAGAATCTGGAGCCTCCGTCATGGCCACCTGCTCACA
ACCATACCCTCCCCATACCCCGCCTCGGAGAACGACATTCCCAGTGTGGCCTTCTCTTCTCGCCTCGGGGGCTTCCGAGGAGCACCAGGGCTGCTCATGGCTGTC
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>DCAF4L2|138009|protein
MESKRPRLLEEADKQKKTVRVGLNAPSMLRKNQLGFLRFANYCRIARELRVSCMQRKKVQIHSWDPSSLASDRFNRILANTNTDQLFTVNQVEAGGSKYGIITMR
GLTTPELRVYPHKTLYVPNRKVNSMCWASLNHLDSHLLLCFVGLADTPSCAVLLPASLFIGSFPGMRRPGMLCSFQIPDAWSCAWSLSIHAYHSFSTGLSQQVLL
TNVVTGHQQSFGTSSDVLAQQFAIMTPLLFNGCRSGEIFGIDLRCGNQGSGWKAICLSHDSAVTSLQILQDGQFLVSSDMTGTIKLWDLRATKCVTQYEGHVNNS
AYLPVHVNEEEGVVAAVGQDCYTRIWSLRHGHLLTTIPSPYPASENDIPSVAFSSRLGGFRGAPGLLMAVREDLYCFSYG
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MESKRPRLLEEADKQKKTVRVGLNAPSMLRKNQLGFLRFANYCRIARELRVSCMQRKKVQIHSWDPSSLASDRFNRILANTNTDQLFTVNQVEAGGSKYGIITMR
GLTTPELRVYPHKTLYVPNRKVNSMCWASLNHLDSHLLLCFVGLADTPSCAVLLPASLFIGSFPGMRRPGMLCSFQIPDAWSCAWSLSIHAYHSFSTGLSQQVLL
TNVVTGHQQSFGTSSDVLAQQFAIMTPLLFNGCRSGEIFGIDLRCGNQGSGWKAICLSHDSAVTSLQILQDGQFLVSSDMTGTIKLWDLRATKCVTQYEGHVNNS
AYLPVHVNEEEGVVAAVGQDCYTRIWSLRHGHLLTTIPSPYPASENDIPSVAFSSRLGGFRGAPGLLMAVREDLYCFSYG
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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 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |
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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