AutismKB 2.0

Evidence Details for C3orf18


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Basic Information Top
Gene Symbol:C3orf18 ( G20 )
Gene Full Name: chromosome 3 open reading frame 18
Band: 3p21.31
Quick LinksEntrez ID:51161; OMIM: NA; Uniprot ID:CC018_HUMAN; ENSEMBL ID: ENSG00000088543; HGNC ID: 24837
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C3orf18|51161|nucleotide
ATGAACTCCAGGACCGCATCTGCTAGGGGCTGGTTCAGCAGCCGCCCACCCACCTCTGAGTCTGACCTGGAACCTGCCACAGATGGGCCAGCCTCCGAGACCACT
ACCCTCAGCCCAGAGGCCACCACCTTTAATGACACCAGAATCCCTGATGCAGCTGGTGGCACGGCCGGCGTGGGTACCATGCTTCTGTCCTTTGGGATCATCACG
GTGATAGGCCTGGCTGTGGCCTTGGTTTTGTACATCAGGAAGAAGAAGAGGCTGGAGAAGCTACGCCACCAGCTCATGCCCATGTACAACTTCGACCCCACGGAG
GAACAAGATGAGTTGGAGCAGGAGCTGCTGGAGCATGGGCGGGACGCCGCCTCTGTACAGGCTGCTACTTCTGTGCAGGCCATGCAGGGCAAGACTACTCTGCCC
TCCCAGGGCCCACTGCAGAGACCCAGCCGGCTGGTGTTTACCGATGTGGCCAATGCCATCCATGCGTGA






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>C3orf18|51161|protein
MNSRTASARGWFSSRPPTSESDLEPATDGPASETTTLSPEATTFNDTRIPDAAGGTAGVGTMLLSFGIITVIGLAVALVLYIRKKKRLEKLRHQLMPMYNFDPTE
EQDELEQELLEHGRDAASVQAATSVQAMQGKTTLPSQGPLQRPSRLVFTDVANAIHA



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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) 1 (1) 0 (0) 0 (0) 0 (0) 0 (0) 1 (1)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top