Evidence Details for FOXI3
Basic Information Top
Gene Symbol: | FOXI3 ( - ) |
---|---|
Gene Full Name: | forkhead box I3 |
Band: | 2p11.2 |
Quick Links | Entrez ID:344167; OMIM: 612351; Uniprot ID:FOXI3_HUMAN; ENSEMBL ID: ; HGNC ID: 35123 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FOXI3|344167|nucleotide
ATGGCCCTCTACTGCGGCGACAACTTCGGAGTGTATTCGCAGCCCGGCCTGCCCCCGCCCGCCGCCACCGCCGCCGCCCCGGGCGCCCCCCCGGCAGCCAGGGCG
CCTTACGGGCTGGCCGACTACGCCGCGCCGCCGGCCGCCGCCGCCAACCCCTACCTGTGGCTCAACGGGCCCGGCGTGGGAGGCCCGCCCTCCGCCGCCGCCGCA
GCCGCCGCCGCGTACCTGGGCGCTCCGCCGCCGCCGCCGCCCCCCGGGGCCGCGGCCGGGCCCTTTCTGCAGCCACCGCCTGCCGCCGGCACCTTCGGCTGCTCT
CAGCGGCCCTTCGCGCAGCCCGCGCCCGCCGCGCCCGCCTCGCCCGCCGCGCCCGCGGGGCCCGGGGAGCTGGGCTGGCTGTCCATGGCCAGCCGCGAGGACCTG
ATGAAGATGGTGCGGCCGCCCTACTCGTATTCGGCGCTCATCGCCATGGCCATTCAGAGCGCGCCCGAGCGCAAACTCACTCTCAGCCACATCTACCAGTTCGTC
GCCGATAGCTTCCCCTTCTACCAGCGCAGCAAGGCCGGCTGGCAGAACTCCATCCGCCACAACCTGTCGCTCAACGACTGCTTCAAGAAGGTGCCCCGCGACGAG
GACGACCCAGGAAAGGGTAATTATTGGACTCTTGATCCGAACTGCGAGAAAATGTTTGACAATGGGAACTTCCGTCGGAAGCGAAAGCGCCGCTCTGAGGCCAGC
AATGGCTCCACAGTGGCTGCTGGGACATCAAAGTCCGAAGAAGGGCTCTCCTCAGGATTGGGGTCTGGAGTGGGTGGGAAGCCAGAAGAAGAGAGCCCCTCCACT
CTGCTGAGGCCTTCCCACTCCCCAGAGCCTCCGGAGGGCACCAAGAGTACTGCCTCATCTCCTGGAGGACCCATGCTCACCTCCACCCCTTGTCTCAACACTTTC
TTCAGCAGCCTCAGCTCCTTGAGTGTCAGCAGCAGTGTGAGTACCCAGCGGGCTCTCCCTGGCAGCCGCCACCTAGGGATCCAGGGGGCCCAGCTGCCCTCCAGC
GGCGTGTTCTCCCCGACCTCCATCTCAGAGGCCTCAGCAGACACCTTGCAACTGAGCAATAGCACCAGCAATAGCACCGGCCAGAGATCTTCCTATTACAGCCCT
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ATGGCCCTCTACTGCGGCGACAACTTCGGAGTGTATTCGCAGCCCGGCCTGCCCCCGCCCGCCGCCACCGCCGCCGCCCCGGGCGCCCCCCCGGCAGCCAGGGCG
CCTTACGGGCTGGCCGACTACGCCGCGCCGCCGGCCGCCGCCGCCAACCCCTACCTGTGGCTCAACGGGCCCGGCGTGGGAGGCCCGCCCTCCGCCGCCGCCGCA
GCCGCCGCCGCGTACCTGGGCGCTCCGCCGCCGCCGCCGCCCCCCGGGGCCGCGGCCGGGCCCTTTCTGCAGCCACCGCCTGCCGCCGGCACCTTCGGCTGCTCT
CAGCGGCCCTTCGCGCAGCCCGCGCCCGCCGCGCCCGCCTCGCCCGCCGCGCCCGCGGGGCCCGGGGAGCTGGGCTGGCTGTCCATGGCCAGCCGCGAGGACCTG
ATGAAGATGGTGCGGCCGCCCTACTCGTATTCGGCGCTCATCGCCATGGCCATTCAGAGCGCGCCCGAGCGCAAACTCACTCTCAGCCACATCTACCAGTTCGTC
GCCGATAGCTTCCCCTTCTACCAGCGCAGCAAGGCCGGCTGGCAGAACTCCATCCGCCACAACCTGTCGCTCAACGACTGCTTCAAGAAGGTGCCCCGCGACGAG
GACGACCCAGGAAAGGGTAATTATTGGACTCTTGATCCGAACTGCGAGAAAATGTTTGACAATGGGAACTTCCGTCGGAAGCGAAAGCGCCGCTCTGAGGCCAGC
AATGGCTCCACAGTGGCTGCTGGGACATCAAAGTCCGAAGAAGGGCTCTCCTCAGGATTGGGGTCTGGAGTGGGTGGGAAGCCAGAAGAAGAGAGCCCCTCCACT
CTGCTGAGGCCTTCCCACTCCCCAGAGCCTCCGGAGGGCACCAAGAGTACTGCCTCATCTCCTGGAGGACCCATGCTCACCTCCACCCCTTGTCTCAACACTTTC
TTCAGCAGCCTCAGCTCCTTGAGTGTCAGCAGCAGTGTGAGTACCCAGCGGGCTCTCCCTGGCAGCCGCCACCTAGGGATCCAGGGGGCCCAGCTGCCCTCCAGC
GGCGTGTTCTCCCCGACCTCCATCTCAGAGGCCTCAGCAGACACCTTGCAACTGAGCAATAGCACCAGCAATAGCACCGGCCAGAGATCTTCCTATTACAGCCCT
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>FOXI3|344167|protein
MALYCGDNFGVYSQPGLPPPAATAAAPGAPPAARAPYGLADYAAPPAAAANPYLWLNGPGVGGPPSAAAAAAAAYLGAPPPPPPPGAAAGPFLQPPPAAGTFGCS
QRPFAQPAPAAPASPAAPAGPGELGWLSMASREDLMKMVRPPYSYSALIAMAIQSAPERKLTLSHIYQFVADSFPFYQRSKAGWQNSIRHNLSLNDCFKKVPRDE
DDPGKGNYWTLDPNCEKMFDNGNFRRKRKRRSEASNGSTVAAGTSKSEEGLSSGLGSGVGGKPEEESPSTLLRPSHSPEPPEGTKSTASSPGGPMLTSTPCLNTF
FSSLSSLSVSSSVSTQRALPGSRHLGIQGAQLPSSGVFSPTSISEASADTLQLSNSTSNSTGQRSSYYSPFPASTSGGQSSPFSSPFHNFSMVNSLIYPREGSEV
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MALYCGDNFGVYSQPGLPPPAATAAAPGAPPAARAPYGLADYAAPPAAAANPYLWLNGPGVGGPPSAAAAAAAAYLGAPPPPPPPGAAAGPFLQPPPAAGTFGCS
QRPFAQPAPAAPASPAAPAGPGELGWLSMASREDLMKMVRPPYSYSALIAMAIQSAPERKLTLSHIYQFVADSFPFYQRSKAGWQNSIRHNLSLNDCFKKVPRDE
DDPGKGNYWTLDPNCEKMFDNGNFRRKRKRRSEASNGSTVAAGTSKSEEGLSSGLGSGVGGKPEEESPSTLLRPSHSPEPPEGTKSTASSPGGPMLTSTPCLNTF
FSSLSSLSVSSSVSTQRALPGSRHLGIQGAQLPSSGVFSPTSISEASADTLQLSNSTSNSTGQRSSYYSPFPASTSGGQSSPFSSPFHNFSMVNSLIYPREGSEV
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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 |
---|---|---|---|---|
Krumm N, 2015 | 2377 | 1373 | 77 | Excess of rare, inherited truncating mutations in autism |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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