Evidence Details for ANO8
Basic Information Top
Gene Symbol: | ANO8 ( KIAA1623,TMEM16H ) |
---|---|
Gene Full Name: | anoctamin 8 |
Band: | 19p13.11 |
Quick Links | Entrez ID:57719; OMIM: 610216; Uniprot ID:ANO8_HUMAN; ENSEMBL ID: ENSG00000074855; HGNC ID: 29329 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ANO8|57719|nucleotide
ATGGCCGAGGCCGCCTCCGGCGCCGGGGGCACGTCCCTGGAGGGCGAGCGTGGCAAGAGGCCCCCGCCGGAGGGCGAGCCTGCAGCCCCGGCGTCCGGAGTTCTG
GATAAGCTTTTCGGAAAGCGGCTCCTGCAGGCTGGTCGCTACCTGGTGTCCCACAAGGCGTGGATGAAGACGGTGCCTACAGAGAACTGCGACGTGCTGATGACC
TTCCCAGACACGACCGATGACCACACGCTGCTATGGCTGCTGAACCACATCCGCGTGGGCATTCCCGAGCTCATCGTGCAAGTCCGCCACCACCGCCACACGCGT
GCCTACGCCTTCTTTGTCACCGCCACGTATGAGAGCCTACTCCGAGGGGCCGACGAGCTGGGTCTGCGCAAAGCAGTGAAGGCCGAGTTTGGCGGGGGCACCCGC
GGCTTCTCCTGCGAGGAGGACTTTATCTATGAGAATGTGGAGAGCGAGCTACGCTTCTTCACCTCCCAGGAACGCCAGAGCATCATCCGCTTCTGGCTGCAGAAT
TTGCGTGCCAAGCAGGGAGAAGCACTCCACAACGTGCGCTTCCTGGAGGACCAGCCAATCATCCCGGAGCTGGCAGCACGTGGGATCATCCAGCAGGTGTTCCCT
GTCCACGAGCAGCGTATTCTGAACCGCCTCATGAAGTCATGGGTGCAGGCCGTGTGTGAAAACCAGCCTCTAGATGACATCTGTGATTACTTTGGTGTGAAAATT
GCCATGTACTTCGCCTGGCTGGGCTTCTACACGTCGGCTATGGTATACCCAGCTGTCTTCGGGTCTGTCCTGTACACATTCACAGAGGCTGATCAGACAAGCCGG
GATGTTTCCTGCGTGGTCTTTGCCCTCTTCAACGTGATCTGGTCGACGCTGTTCCTAGAGGAATGGAAGCGGAGAGGGGCTGAGCTGGCATATAAGTGGGGGACG
CTGGACTCACCTGGGGAAGCCGTGGAGGAGCCACGCCCCCAGTTCAGGGGCGTGCGACGTATCAGCCCCATCACGCGGGCCGAGGAGTTCTACTACCCGCCCTGG
AAGCGGCTGCTCTTCCAGCTGCTTGTGAGCCTCCCCCTGTGCCTGGCGTGCCTCGTCTGTGTCTTCTTGCTCATGCTTGGCTGCTTCCAGCTGCAGGAGCTGGTG
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ATGGCCGAGGCCGCCTCCGGCGCCGGGGGCACGTCCCTGGAGGGCGAGCGTGGCAAGAGGCCCCCGCCGGAGGGCGAGCCTGCAGCCCCGGCGTCCGGAGTTCTG
GATAAGCTTTTCGGAAAGCGGCTCCTGCAGGCTGGTCGCTACCTGGTGTCCCACAAGGCGTGGATGAAGACGGTGCCTACAGAGAACTGCGACGTGCTGATGACC
TTCCCAGACACGACCGATGACCACACGCTGCTATGGCTGCTGAACCACATCCGCGTGGGCATTCCCGAGCTCATCGTGCAAGTCCGCCACCACCGCCACACGCGT
GCCTACGCCTTCTTTGTCACCGCCACGTATGAGAGCCTACTCCGAGGGGCCGACGAGCTGGGTCTGCGCAAAGCAGTGAAGGCCGAGTTTGGCGGGGGCACCCGC
GGCTTCTCCTGCGAGGAGGACTTTATCTATGAGAATGTGGAGAGCGAGCTACGCTTCTTCACCTCCCAGGAACGCCAGAGCATCATCCGCTTCTGGCTGCAGAAT
TTGCGTGCCAAGCAGGGAGAAGCACTCCACAACGTGCGCTTCCTGGAGGACCAGCCAATCATCCCGGAGCTGGCAGCACGTGGGATCATCCAGCAGGTGTTCCCT
GTCCACGAGCAGCGTATTCTGAACCGCCTCATGAAGTCATGGGTGCAGGCCGTGTGTGAAAACCAGCCTCTAGATGACATCTGTGATTACTTTGGTGTGAAAATT
GCCATGTACTTCGCCTGGCTGGGCTTCTACACGTCGGCTATGGTATACCCAGCTGTCTTCGGGTCTGTCCTGTACACATTCACAGAGGCTGATCAGACAAGCCGG
GATGTTTCCTGCGTGGTCTTTGCCCTCTTCAACGTGATCTGGTCGACGCTGTTCCTAGAGGAATGGAAGCGGAGAGGGGCTGAGCTGGCATATAAGTGGGGGACG
CTGGACTCACCTGGGGAAGCCGTGGAGGAGCCACGCCCCCAGTTCAGGGGCGTGCGACGTATCAGCCCCATCACGCGGGCCGAGGAGTTCTACTACCCGCCCTGG
AAGCGGCTGCTCTTCCAGCTGCTTGTGAGCCTCCCCCTGTGCCTGGCGTGCCTCGTCTGTGTCTTCTTGCTCATGCTTGGCTGCTTCCAGCTGCAGGAGCTGGTG
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>ANO8|57719|protein
MAEAASGAGGTSLEGERGKRPPPEGEPAAPASGVLDKLFGKRLLQAGRYLVSHKAWMKTVPTENCDVLMTFPDTTDDHTLLWLLNHIRVGIPELIVQVRHHRHTR
AYAFFVTATYESLLRGADELGLRKAVKAEFGGGTRGFSCEEDFIYENVESELRFFTSQERQSIIRFWLQNLRAKQGEALHNVRFLEDQPIIPELAARGIIQQVFP
VHEQRILNRLMKSWVQAVCENQPLDDICDYFGVKIAMYFAWLGFYTSAMVYPAVFGSVLYTFTEADQTSRDVSCVVFALFNVIWSTLFLEEWKRRGAELAYKWGT
LDSPGEAVEEPRPQFRGVRRISPITRAEEFYYPPWKRLLFQLLVSLPLCLACLVCVFLLMLGCFQLQELVLSVKGLPRLARFLPKVMLALLVSVSAEGYKKLAIW
LNDMENYRLESAYEKHLIIKVVLFQFVNSYLSLFYIGFYLKDMERLKEMLATLLITRQFLQNVREVLQPHLYRRLGRGELGLRAVWELARALLGLLSLRRPAPRR
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MAEAASGAGGTSLEGERGKRPPPEGEPAAPASGVLDKLFGKRLLQAGRYLVSHKAWMKTVPTENCDVLMTFPDTTDDHTLLWLLNHIRVGIPELIVQVRHHRHTR
AYAFFVTATYESLLRGADELGLRKAVKAEFGGGTRGFSCEEDFIYENVESELRFFTSQERQSIIRFWLQNLRAKQGEALHNVRFLEDQPIIPELAARGIIQQVFP
VHEQRILNRLMKSWVQAVCENQPLDDICDYFGVKIAMYFAWLGFYTSAMVYPAVFGSVLYTFTEADQTSRDVSCVVFALFNVIWSTLFLEEWKRRGAELAYKWGT
LDSPGEAVEEPRPQFRGVRRISPITRAEEFYYPPWKRLLFQLLVSLPLCLACLVCVFLLMLGCFQLQELVLSVKGLPRLARFLPKVMLALLVSVSAEGYKKLAIW
LNDMENYRLESAYEKHLIIKVVLFQFVNSYLSLFYIGFYLKDMERLKEMLATLLITRQFLQNVREVLQPHLYRRLGRGELGLRAVWELARALLGLLSLRRPAPRR
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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) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (2) | 0 (0) | 0 (0) | 4 (3) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
McCauley, 2005 | - | microsatellite-based genomic screen | autism | 158 | - | 158 | - | 333 | - | - |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
Reference | Case Number | Family Number | Mosaic Number | Title |
---|---|---|---|---|
Dou Y, 2017 | - | 2361 | 230 | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and |
Krupp DR, 2017 | - | 2264 | 247 | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
NGS Other Studies Top
Low Scale Gene Studies Top
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