AutismKB 2.0

Evidence Details for C13orf16


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Basic Information Top
Gene Symbol:C13orf16 ( MGC35169,bA474D23.1 )
Gene Full Name: chromosome 13 open reading frame 16
Band: 13q34
Quick LinksEntrez ID:121793; OMIM: NA; Uniprot ID:CM016_HUMAN; ENSEMBL ID: ENSG00000153495; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>C13orf16|121793|nucleotide
ATGGAATACGTGCTGGAAGTGAAGAACTCTCCGCGGCACCTCCTGAAGCAATTCACAGTGTGTGATGTTCCTCTGTATGACATTTGTGACTACAACGTCTCCAGG
GACCGATGCCAGGAGCTCGGGTGCTGCTTCTACGAAGGCGTCTGCTACAAGAAAGCGGTTCCCATTTACATCCACGTGTTCTCTGCCTTGATTGTGATCATCGCT
GGGGCCTTCGTCATCACCATCATCTACAGAGTCATTCAGGAGAGCAGGAAAGAAAAGGCCATCCCTGTGGATGTCGCGCTGCCACAGAAGTCCAGCGAAAAGGCG
GAGTTGGCCTCATCCAGCAGCAAGTTAGGGCTGAAGCCTGCGAGTCCTGGGCCTCCAAGTGCTGGGCCCTCGATGAAGAGTGACGAGGATAAGGATGATGTAACA
GGGACAATAACAGAAGCCGAAGAAACTGAGGACTGA






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>C13orf16|121793|protein
MEYVLEVKNSPRHLLKQFTVCDVPLYDICDYNVSRDRCQELGCCFYEGVCYKKAVPIYIHVFSALIVIIAGAFVITIIYRVIQESRKEKAIPVDVALPQKSSEKA
ELASSSSKLGLKPASPGPPSAGPSMKSDEDKDDVTGTITEAEETED



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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