Evidence Details for FRMD4A
Basic Information Top
Gene Symbol: | FRMD4A ( FLJ10210,FRMD4,KIAA1294,bA295P9.4 ) |
---|---|
Gene Full Name: | FERM domain containing 4A |
Band: | 10p13 |
Quick Links | Entrez ID:55691; OMIM: NA; Uniprot ID:FRM4A_HUMAN; ENSEMBL ID: ENSG00000151474; HGNC ID: 25491 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FRMD4A|55691|nucleotide
ATGGCAGTGCAGCTGGTGCCCGACTCAGCTCTCGGCCTGCTGATGATGACGGAGGGCCGCCGATGTCAAGTACATCTTCTTGATGACAGGAAGCTGGAACTCCTA
GTACAGCCCAAGCTGTTGGCCAAGGAGCTTCTTGACCTTGTGGCTTCTCACTTCAATCTGAAGGAAAAGGAGTACTTTGGAATAGCATTCACAGATGAAACGGGA
CACTTAAACTGGCTTCAGCTAGATCGAAGAGTATTGGAACATGACTTCCCTAAAAAGTCAGGACCCGTGGTTTTATACTTTTGTGTCAGGTTCTATATAGAAAGC
ATTTCATACCTGAAGGATAATGCTACCATTGAGCTTTTCTTTCTGAACGCGAAGTCCTGCATCTACAAGGAGCTTATTGACGTTGACAGCGAAGTGGTGTTTGAA
TTAGCTTCCTATATTTTACAGGAGGCAAAGGGAGATTTTTCTAGCAATGAAGTTGTGAGGAGTGACTTGAAGAAGCTGCCAGCCCTTCCCACCCAAGCCCTGAAG
GAGCACCCTTCCCTGGCCTACTGTGAAGACAGAGTCATTGAGCACTACAAGAAACTGAACGGTCAGACAAGAGGTCAAGCAATCGTAAACTACATGAGCATCGTG
GAGTCTCTCCCAACCTACGGGGTTCACTATTATGCAGTGAAGGACAAGCAGGGCATACCATGGTGGCTGGGCCTGAGCTACAAAGGGATCTTCCAGTATGACTAC
CATGATAAAGTGAAGCCAAGAAAGATATTCCAATGGAGACAGTTGGAAAACCTGTACTTCAGAGAAAAGAAGTTTTCCGTGGAAGTTCATGACCCACGCAGGGCT
TCAGTGACAAGGAGGACGTTTGGGCACAGCGGCATTGCAGTGCACACGTGGTATGCATGTCCGGCATTGATCAAGTCCATCTGGGCTATGGCCATAAGCCAACAC
CAGTTCTATCTGGACAGAAAGCAGAGTAAGTCCAAAATCCATGCAGCACGCAGCCTGAGTGAGATCGCCATCGACCTGACCGAGACGGGGACGCTGAAGACCTCG
AAGCTGGCCAACATGGGTAGCAAGGGGAAGATCATCAGCGGCAGCAGCGGCAGCCTGCTGTCTTCAGGTTCTCAGGAATCAGATAGCTCGCAGTCGGCCAAGAAG
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ATGGCAGTGCAGCTGGTGCCCGACTCAGCTCTCGGCCTGCTGATGATGACGGAGGGCCGCCGATGTCAAGTACATCTTCTTGATGACAGGAAGCTGGAACTCCTA
GTACAGCCCAAGCTGTTGGCCAAGGAGCTTCTTGACCTTGTGGCTTCTCACTTCAATCTGAAGGAAAAGGAGTACTTTGGAATAGCATTCACAGATGAAACGGGA
CACTTAAACTGGCTTCAGCTAGATCGAAGAGTATTGGAACATGACTTCCCTAAAAAGTCAGGACCCGTGGTTTTATACTTTTGTGTCAGGTTCTATATAGAAAGC
ATTTCATACCTGAAGGATAATGCTACCATTGAGCTTTTCTTTCTGAACGCGAAGTCCTGCATCTACAAGGAGCTTATTGACGTTGACAGCGAAGTGGTGTTTGAA
TTAGCTTCCTATATTTTACAGGAGGCAAAGGGAGATTTTTCTAGCAATGAAGTTGTGAGGAGTGACTTGAAGAAGCTGCCAGCCCTTCCCACCCAAGCCCTGAAG
GAGCACCCTTCCCTGGCCTACTGTGAAGACAGAGTCATTGAGCACTACAAGAAACTGAACGGTCAGACAAGAGGTCAAGCAATCGTAAACTACATGAGCATCGTG
GAGTCTCTCCCAACCTACGGGGTTCACTATTATGCAGTGAAGGACAAGCAGGGCATACCATGGTGGCTGGGCCTGAGCTACAAAGGGATCTTCCAGTATGACTAC
CATGATAAAGTGAAGCCAAGAAAGATATTCCAATGGAGACAGTTGGAAAACCTGTACTTCAGAGAAAAGAAGTTTTCCGTGGAAGTTCATGACCCACGCAGGGCT
TCAGTGACAAGGAGGACGTTTGGGCACAGCGGCATTGCAGTGCACACGTGGTATGCATGTCCGGCATTGATCAAGTCCATCTGGGCTATGGCCATAAGCCAACAC
CAGTTCTATCTGGACAGAAAGCAGAGTAAGTCCAAAATCCATGCAGCACGCAGCCTGAGTGAGATCGCCATCGACCTGACCGAGACGGGGACGCTGAAGACCTCG
AAGCTGGCCAACATGGGTAGCAAGGGGAAGATCATCAGCGGCAGCAGCGGCAGCCTGCTGTCTTCAGGTTCTCAGGAATCAGATAGCTCGCAGTCGGCCAAGAAG
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>FRMD4A|55691|protein
MAVQLVPDSALGLLMMTEGRRCQVHLLDDRKLELLVQPKLLAKELLDLVASHFNLKEKEYFGIAFTDETGHLNWLQLDRRVLEHDFPKKSGPVVLYFCVRFYIES
ISYLKDNATIELFFLNAKSCIYKELIDVDSEVVFELASYILQEAKGDFSSNEVVRSDLKKLPALPTQALKEHPSLAYCEDRVIEHYKKLNGQTRGQAIVNYMSIV
ESLPTYGVHYYAVKDKQGIPWWLGLSYKGIFQYDYHDKVKPRKIFQWRQLENLYFREKKFSVEVHDPRRASVTRRTFGHSGIAVHTWYACPALIKSIWAMAISQH
QFYLDRKQSKSKIHAARSLSEIAIDLTETGTLKTSKLANMGSKGKIISGSSGSLLSSGSQESDSSQSAKKDMLAALKSRQEALEETLRQRLEELKKLCLREAELT
GKLPVEYPLDPGEEPPIVRRRIGTAFKLDEQKILPKGEEAELERLEREFAIQSQITEAARRLASDPNVSKKLKKQRKTSYLNALKKLQEIENAINENRIKSGKKP
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MAVQLVPDSALGLLMMTEGRRCQVHLLDDRKLELLVQPKLLAKELLDLVASHFNLKEKEYFGIAFTDETGHLNWLQLDRRVLEHDFPKKSGPVVLYFCVRFYIES
ISYLKDNATIELFFLNAKSCIYKELIDVDSEVVFELASYILQEAKGDFSSNEVVRSDLKKLPALPTQALKEHPSLAYCEDRVIEHYKKLNGQTRGQAIVNYMSIV
ESLPTYGVHYYAVKDKQGIPWWLGLSYKGIFQYDYHDKVKPRKIFQWRQLENLYFREKKFSVEVHDPRRASVTRRTFGHSGIAVHTWYACPALIKSIWAMAISQH
QFYLDRKQSKSKIHAARSLSEIAIDLTETGTLKTSKLANMGSKGKIISGSSGSLLSSGSQESDSSQSAKKDMLAALKSRQEALEETLRQRLEELKKLCLREAELT
GKLPVEYPLDPGEEPPIVRRRIGTAFKLDEQKILPKGEEAELERLEREFAIQSQITEAARRLASDPNVSKKLKKQRKTSYLNALKKLQEIENAINENRIKSGKKP
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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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