Evidence Details for AKNA


Gene Symbol: | AKNA ( FLJ31001,FLJ33184,KIAA1968,RP11-82I1.4 ) |
---|---|
Gene Full Name: | AT-hook transcription factor |
Band: | 9q32 |
Quick Links | Entrez ID:80709; OMIM: 605729; Uniprot ID:AKNA_HUMAN; ENSEMBL ID: ENSG00000106948; HGNC ID: 24108 |
Relate to Another Database: | SFARIGene; denovo-db |


>AKNA|80709|nucleotide
ATGGCCAGCTCGGAGACTGAGATCCGCTGGGCTGAGCCTGGCCTGGGGAAGGGCCCCCAGCGGCGGCGCTGGGCCTGGGCCGAGGACAAGAGGGATGTGGATAGA
AGTAGTTCACAAAGCTGGGAAGAAGAGAGACTCTTTCCCAATGCCACCAGCCCCGAGCTCCTAGAGGACTTCCGCCTGGCCCAGCAGCACCTGCCGCCCCTGGAG
TGGGACCCACACCCGCAGCCCGATGGGCATCAGGATTCCGAGTCAGGAGAGACTTCGGGAGAAGAGGCTGAAGCAGAGGATGTGGACAGCCCAGCAAGTTCCCAT
GAGCCTCTTGCCTGGCTCCCCCAGCAGGGCCGTCAGCTGGACATGACTGAAGAGGAGCCAGATGGGACCCTCGGAAGTCTGGAGGTTGAGGAGGCTGGAGAGAGC
TCCTCAAGGTTGGGGTATGAGGCTGGTCTCAGCTTGGAAGGCCATGGAAACACCAGCCCCATGGCTCTTGGGCATGGTCAGGCCAGGGGCTGGGTGGCTTCTGGC
GAACAAGCCAGTGGGGACAAACTTTCTGAACATTCCGAGGTCAACCCATCCGTTGAACTCAGCCCGGCAAGGTCCTGGAGCAGTGGGACAGTGAGCCTCGACCAC
CCTAGTGACAGCCTTGATTCTACCTGGGAAGGAGAGACCGATGGCCCCCAGCCCACTGCCCTGGCAGAAACCTTGCCAGAGGGCCCCAGCCACCACCTCCTAAGC
CCAGATGGCAGAACTGGAGGCAGTGTTGCTCGGGCAACCCCCATGGAATTCCAGGACTCCTCAGCTCCCCCAGCCCAGAGTCCGCAGCATGCCACAGATAGATGG
AGGAGAGAAACGACCAGATTCTTCTGCCCTCAGCCCAAGGAACACATCTGGAAGCAGACAAAGACGTCACCTAAGCCACTCCCTTCCCGATTCATTGGCTCCATC
AGCCCCCTGAATCCCCAGCCCAGGCCAACGCGGCAGGGCAGGCCGCTGCCCAGACAGGGAGCCACTCTGGCTGGCCGCTCCTCTTCTAATGCCCCCAAGTATGGC
CGGGGGCAGTTGAACTACCCACTCCCTGATTTCTCCAAGGTAGGGCCCCGGGTGAGATTCCCCAAAGATGAGAGCTACCGTCCCCCCAAGTCCAGAAGCCACAAC
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ATGGCCAGCTCGGAGACTGAGATCCGCTGGGCTGAGCCTGGCCTGGGGAAGGGCCCCCAGCGGCGGCGCTGGGCCTGGGCCGAGGACAAGAGGGATGTGGATAGA
AGTAGTTCACAAAGCTGGGAAGAAGAGAGACTCTTTCCCAATGCCACCAGCCCCGAGCTCCTAGAGGACTTCCGCCTGGCCCAGCAGCACCTGCCGCCCCTGGAG
TGGGACCCACACCCGCAGCCCGATGGGCATCAGGATTCCGAGTCAGGAGAGACTTCGGGAGAAGAGGCTGAAGCAGAGGATGTGGACAGCCCAGCAAGTTCCCAT
GAGCCTCTTGCCTGGCTCCCCCAGCAGGGCCGTCAGCTGGACATGACTGAAGAGGAGCCAGATGGGACCCTCGGAAGTCTGGAGGTTGAGGAGGCTGGAGAGAGC
TCCTCAAGGTTGGGGTATGAGGCTGGTCTCAGCTTGGAAGGCCATGGAAACACCAGCCCCATGGCTCTTGGGCATGGTCAGGCCAGGGGCTGGGTGGCTTCTGGC
GAACAAGCCAGTGGGGACAAACTTTCTGAACATTCCGAGGTCAACCCATCCGTTGAACTCAGCCCGGCAAGGTCCTGGAGCAGTGGGACAGTGAGCCTCGACCAC
CCTAGTGACAGCCTTGATTCTACCTGGGAAGGAGAGACCGATGGCCCCCAGCCCACTGCCCTGGCAGAAACCTTGCCAGAGGGCCCCAGCCACCACCTCCTAAGC
CCAGATGGCAGAACTGGAGGCAGTGTTGCTCGGGCAACCCCCATGGAATTCCAGGACTCCTCAGCTCCCCCAGCCCAGAGTCCGCAGCATGCCACAGATAGATGG
AGGAGAGAAACGACCAGATTCTTCTGCCCTCAGCCCAAGGAACACATCTGGAAGCAGACAAAGACGTCACCTAAGCCACTCCCTTCCCGATTCATTGGCTCCATC
AGCCCCCTGAATCCCCAGCCCAGGCCAACGCGGCAGGGCAGGCCGCTGCCCAGACAGGGAGCCACTCTGGCTGGCCGCTCCTCTTCTAATGCCCCCAAGTATGGC
CGGGGGCAGTTGAACTACCCACTCCCTGATTTCTCCAAGGTAGGGCCCCGGGTGAGATTCCCCAAAGATGAGAGCTACCGTCCCCCCAAGTCCAGAAGCCACAAC
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>AKNA|80709|protein
MASSETEIRWAEPGLGKGPQRRRWAWAEDKRDVDRSSSQSWEEERLFPNATSPELLEDFRLAQQHLPPLEWDPHPQPDGHQDSESGETSGEEAEAEDVDSPASSH
EPLAWLPQQGRQLDMTEEEPDGTLGSLEVEEAGESSSRLGYEAGLSLEGHGNTSPMALGHGQARGWVASGEQASGDKLSEHSEVNPSVELSPARSWSSGTVSLDH
PSDSLDSTWEGETDGPQPTALAETLPEGPSHHLLSPDGRTGGSVARATPMEFQDSSAPPAQSPQHATDRWRRETTRFFCPQPKEHIWKQTKTSPKPLPSRFIGSI
SPLNPQPRPTRQGRPLPRQGATLAGRSSSNAPKYGRGQLNYPLPDFSKVGPRVRFPKDESYRPPKSRSHNRKPQAPARPLIFKSPAEIVQEVLLSSGEAALAKDT
PPAHPITRVPQEFQTPEQATELVHQLQEDYHRLLTKYAEAENTIDQLRLGAKVNLFSDPPQPNHSIHTGMVPQGTKVLSFTIPQPRSAEWWPGPAEDPQASAASG
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MASSETEIRWAEPGLGKGPQRRRWAWAEDKRDVDRSSSQSWEEERLFPNATSPELLEDFRLAQQHLPPLEWDPHPQPDGHQDSESGETSGEEAEAEDVDSPASSH
EPLAWLPQQGRQLDMTEEEPDGTLGSLEVEEAGESSSRLGYEAGLSLEGHGNTSPMALGHGQARGWVASGEQASGDKLSEHSEVNPSVELSPARSWSSGTVSLDH
PSDSLDSTWEGETDGPQPTALAETLPEGPSHHLLSPDGRTGGSVARATPMEFQDSSAPPAQSPQHATDRWRRETTRFFCPQPKEHIWKQTKTSPKPLPSRFIGSI
SPLNPQPRPTRQGRPLPRQGATLAGRSSSNAPKYGRGQLNYPLPDFSKVGPRVRFPKDESYRPPKSRSHNRKPQAPARPLIFKSPAEIVQEVLLSSGEAALAKDT
PPAHPITRVPQEFQTPEQATELVHQLQEDYHRLLTKYAEAENTIDQLRLGAKVNLFSDPPQPNHSIHTGMVPQGTKVLSFTIPQPRSAEWWPGPAEDPQASAASG
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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) |














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. |






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