Evidence Details for MAP6D1
Basic Information Top
| Gene Symbol: | MAP6D1 ( FLJ12748,MAPO6D1,SL21 ) |
|---|---|
| Gene Full Name: | MAP6 domain containing 1 |
| Band: | 3q27.1 |
| Quick Links | Entrez ID:79929; OMIM: 610593; Uniprot ID:MA6D1_HUMAN; ENSEMBL ID: ENSG00000180834; HGNC ID: 25753 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>MAP6D1|79929|nucleotide
ATGGCGTGGCCCTGTATCAGCCGCCTGTGCTGCCTGGCGCGGCGCTGGAACCAGCTGGACCGCTCCGACGTGGCGGTGCCGCTCACTCTGCACGGCTACTCGGAC
CTCGACAGCGAGGAGCCGGGCACGGGCGGCGCCGCCTCGCGCAGGGGCCAGCCTCCCGCGGGCGCCCGGGATTCCGGCCGGGACGTGCCGCTCACTCAGTACCAG
CGGGACTTCGGCTTGTGGACCACGCCCGCCGGGCCCAAGGATCCGCCGCCGGGGCGCGGACCGGGGGCGGGCGGCCGCAGGGGCAAATCCTCCGCGCAGTCCTCC
GCGCCACCTGCGCCCGGCGCCCGCGGGGTCTACGTGCTGCCCATCGGCGACGCGGACGCGGCTGCAGCAGTGACCACGTCGTACAGACAGGAATTCCAGGCTTGG
ACTGGAGTGAAGCCCTCAAGATCCACAAAGACAAAACCAGCCCGAGTCATCACAACCCACACTTCGGGATGGGACAGCAGCCCTGGGGCCGGCTTCCAGGTCCCA
GAGGTGAGGAAGAAGTTCACTCCTAACCCCTCCGCCATCTTTCAGGCCTCAGCTCCCCGGATTCTCAACGTGTGA
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ATGGCGTGGCCCTGTATCAGCCGCCTGTGCTGCCTGGCGCGGCGCTGGAACCAGCTGGACCGCTCCGACGTGGCGGTGCCGCTCACTCTGCACGGCTACTCGGAC
CTCGACAGCGAGGAGCCGGGCACGGGCGGCGCCGCCTCGCGCAGGGGCCAGCCTCCCGCGGGCGCCCGGGATTCCGGCCGGGACGTGCCGCTCACTCAGTACCAG
CGGGACTTCGGCTTGTGGACCACGCCCGCCGGGCCCAAGGATCCGCCGCCGGGGCGCGGACCGGGGGCGGGCGGCCGCAGGGGCAAATCCTCCGCGCAGTCCTCC
GCGCCACCTGCGCCCGGCGCCCGCGGGGTCTACGTGCTGCCCATCGGCGACGCGGACGCGGCTGCAGCAGTGACCACGTCGTACAGACAGGAATTCCAGGCTTGG
ACTGGAGTGAAGCCCTCAAGATCCACAAAGACAAAACCAGCCCGAGTCATCACAACCCACACTTCGGGATGGGACAGCAGCCCTGGGGCCGGCTTCCAGGTCCCA
GAGGTGAGGAAGAAGTTCACTCCTAACCCCTCCGCCATCTTTCAGGCCTCAGCTCCCCGGATTCTCAACGTGTGA
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>MAP6D1|79929|protein
MAWPCISRLCCLARRWNQLDRSDVAVPLTLHGYSDLDSEEPGTGGAASRRGQPPAGARDSGRDVPLTQYQRDFGLWTTPAGPKDPPPGRGPGAGGRRGKSSAQSS
APPAPGARGVYVLPIGDADAAAAVTTSYRQEFQAWTGVKPSRSTKTKPARVITTHTSGWDSSPGAGFQVPEVRKKFTPNPSAIFQASAPRILNV
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MAWPCISRLCCLARRWNQLDRSDVAVPLTLHGYSDLDSEEPGTGGAASRRGQPPAGARDSGRDVPLTQYQRDFGLWTTPAGPKDPPPGRGPGAGGRRGKSSAQSS
APPAPGARGVYVLPIGDADAAAAVTTSYRQEFQAWTGVKPSRSTKTKPARVITTHTSGWDSSPGAGFQVPEVRKKFTPNPSAIFQASAPRILNV
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Evidence summary TopClick 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) | 1 (1) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 12 (2) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies TopLinkage Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Allen-Brady, 2008 | - | SNP-based genomic screen |  | | ASD | 1 | - | 1 | - | 7 | 22 | 29 |
Low Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS 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 TopNGS Other Studies Top Low Scale Gene Studies TopContact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.