AutismKB 2.0

Evidence Details for C8orf31


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Basic Information Top
Gene Symbol:C8orf31 ( FLJ37131,MGC90155 )
Gene Full Name: chromosome 8 open reading frame 31
Band: 8q24.3
Quick LinksEntrez ID:286122; OMIM: NA; Uniprot ID:CH031_HUMAN; ENSEMBL ID: ENSG00000177335; HGNC ID: 26731
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C8orf31|286122|nucleotide
ATGGCTGAAAAGCCACACCAGAATTCCTGCAATTCAGTGAGGCAGCTCTTCAAAACCAAGCAGCTGGTGACGCACAGGGACAGAGGGAGCTGTACGCACAGGGCC
CAGGGGCTGCTGGCTGCCAGGACCACCGCATTGCAGAGGTCTCCCTTGCAGCAAGAGATCTGGGAGTCCACAACGGCACTTAACCTGCCCTCTGCCCTGGCACCC
CAGGGACTCACTGCCAAAGACGCTCACTTTCTGGGAGACACAGACCCCATCCAGGAAGGGGCACGAGACCACGCTGCAGGAGGCCCCTTCCAAGACCGCCAAGCA
TCTGTAGCAGCGCAGACCCTGAGCTGGGAGAGAGGGCAAGGATTCTCTCGGCACCACGGGAACCACCTTCTCTACTCTCACTGA







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>C8orf31|286122|protein
MAEKPHQNSCNSVRQLFKTKQLVTHRDRGSCTHRAQGLLAARTTALQRSPLQQEIWESTTALNLPSALAPQGLTAKDAHFLGDTDPIQEGARDHAAGGPFQDRQA
SVAAQTLSWERGQGFSRHHGNHLLYSH



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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