AutismKB 2.0

Evidence Details for ANO8


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Basic Information Top
Gene Symbol:ANO8 ( KIAA1623,TMEM16H )
Gene Full Name: anoctamin 8
Band: 19p13.11
Quick LinksEntrez 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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>ANO8|57719|protein
MAEAASGAGGTSLEGERGKRPPPEGEPAAPASGVLDKLFGKRLLQAGRYLVSHKAWMKTVPTENCDVLMTFPDTTDDHTLLWLLNHIRVGIPELIVQVRHHRHTR
AYAFFVTATYESLLRGADELGLRKAVKAEFGGGTRGFSCEEDFIYENVESELRFFTSQERQSIIRFWLQNLRAKQGEALHNVRFLEDQPIIPELAARGIIQQVFP
VHEQRILNRLMKSWVQAVCENQPLDDICDYFGVKIAMYFAWLGFYTSAMVYPAVFGSVLYTFTEADQTSRDVSCVVFALFNVIWSTLFLEEWKRRGAELAYKWGT
LDSPGEAVEEPRPQFRGVRRISPITRAEEFYYPPWKRLLFQLLVSLPLCLACLVCVFLLMLGCFQLQELVLSVKGLPRLARFLPKVMLALLVSVSAEGYKKLAIW
LNDMENYRLESAYEKHLIIKVVLFQFVNSYLSLFYIGFYLKDMERLKEMLATLLITRQFLQNVREVLQPHLYRRLGRGELGLRAVWELARALLGLLSLRRPAPRR
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Evidence summary Top

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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 screenautism 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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Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018