AutismKB 2.0

Evidence Details for C16orf82


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Basic Information Top
Gene Symbol:C16orf82 ( FLJ18616,TNT )
Gene Full Name: chromosome 16 open reading frame 82
Band: 16p12.1
Quick LinksEntrez ID:162083; OMIM: NA; Uniprot ID:TNT_HUMAN; ENSEMBL ID: ENSG00000234186; HGNC ID: 30755
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C16orf82|162083|nucleotide
CTGGATAAACCACTTCAGCTGCCCCCCATTTTTCTCGAGGGAGAAAAAGGGGAATCCTCTGTCCAGAATGAGCAGGAAGGAGAGCCAAGCCTACAGTCACCCAGC
TTAGAGCTCCAGTCCCCTGCGTGGCCACGCCATGCAGGAGTGGCTCAGGAGCCCCTGAAAGTGTCCAGCAGCTACCTCAGTGACACCCAGAGCAGCGAGAGTCAT
GTTTCCAGCGTGCAGCACCCGAGGCCAGAGGAGGGCAGCCATGCCAGCCTGAGCAGCGGGTACGCAGGGGACAAGGAGGGCAGCGACATCAGCTTGGTGGGCAGC
CACCGGAGAGTGCGGCTGAACAGAAGGCTCAACACCCAGGCGGCCAGTAACCAAACCAGCCAGCTGGGCTCCATAGACCCTCCCAGCTCTCTAAAGAGCCGGCTG
ACTGGCCCCGCCCACAGCACCAAGCAGACTGGAGGGAAAGAGTGA






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>C16orf82|162083|protein
MDKPLQLPPIFLEGEKGESSVQNEQEGEPSLQSPSLELQSPAWPRHAGVAQEPLKVSSSYLSDTQSSESHVSSVQHPRPEEGSHASLSSGYAGDKEGSDISLVGS
HRRVRLNRRLNTQAASNQTSQLGSIDPPSSLKSRLTGPAHSTKQTGGKE



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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) 1 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (0) 0 (0) 2 (2)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Yuen RK, 2016 - WGSASD 200 - - - 200 - -
Linkage Studies Top