Evidence Details for C17orf65


Gene Symbol: | C17orf65 ( DKFZp762C2414,MGC119234 ) |
---|---|
Gene Full Name: | chromosome 17 open reading frame 65 |
Band: | 17q21.31 |
Quick Links | Entrez ID:339201; OMIM: NA; Uniprot ID:CQ065_HUMAN; ENSEMBL ID: ENSG00000168597; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |


>C17orf65|339201|nucleotide
ATGTCAGGGCCTCCCAGCGCACCTCAGGGCGCACTGGCTGCGCCCCGTAGTCCAGCAGTGCGGCGAAAAGGACTTCAGGCTCCCAGTTGGGGGAGTCCTGGACGG
CCTGCAGCGCACAGTCCATGGGCGTGTGGCCCGCCCCATTGGGGACCTCAGCGCGGGCCCCGTAACGCAGCAGCAGCTCGGCCAGGCCCCCGCAGCCGTTGGCAC
AAGCGTTGTGCAGCGGCGTGTGGCGCTTGCGCCCGGCCGCCCGGGCATCAGCTCCAGCCTCCAGGAGCCGGCGCGCCGCAGCCTGGTGTCGCCTGCAGCTACCTG
GGCCCTCGGCCCCAGCGCACGCCGTGTTCAGCGCAGTCTCGCCCTGGCTGGTGCGCAGGCCCACGTCGGCGCCATGCTCCAGGTACAGAGCCACATGTTGCTCCA
GGCCGCGCGCCGCCGCCACGTGCAGGGGCGTCTCCTGGCTCTCGCCTGCTGCCAGGTTCACCGTCGCTCCTGCTTCCAGCAGCAACTTGGCGCACCTGGGGACAA
GAGAGCAAGGTCCTGAGGAAAATCCTGAAGGCTTGGGACCCCTTCAGCTTGCTGTGA
Show »
ATGTCAGGGCCTCCCAGCGCACCTCAGGGCGCACTGGCTGCGCCCCGTAGTCCAGCAGTGCGGCGAAAAGGACTTCAGGCTCCCAGTTGGGGGAGTCCTGGACGG
CCTGCAGCGCACAGTCCATGGGCGTGTGGCCCGCCCCATTGGGGACCTCAGCGCGGGCCCCGTAACGCAGCAGCAGCTCGGCCAGGCCCCCGCAGCCGTTGGCAC
AAGCGTTGTGCAGCGGCGTGTGGCGCTTGCGCCCGGCCGCCCGGGCATCAGCTCCAGCCTCCAGGAGCCGGCGCGCCGCAGCCTGGTGTCGCCTGCAGCTACCTG
GGCCCTCGGCCCCAGCGCACGCCGTGTTCAGCGCAGTCTCGCCCTGGCTGGTGCGCAGGCCCACGTCGGCGCCATGCTCCAGGTACAGAGCCACATGTTGCTCCA
GGCCGCGCGCCGCCGCCACGTGCAGGGGCGTCTCCTGGCTCTCGCCTGCTGCCAGGTTCACCGTCGCTCCTGCTTCCAGCAGCAACTTGGCGCACCTGGGGACAA
GAGAGCAAGGTCCTGAGGAAAATCCTGAAGGCTTGGGACCCCTTCAGCTTGCTGTGA
Show »
>C17orf65|339201|protein
MSGPPSAPQGALAAPRSPAVRRKGLQAPSWGSPGRPAAHSPWACGPPHWGPQRGPRNAAAARPGPRSRWHKRCAAACGACARPPGHQLQPPGAGAPQPGVACSYL
GPRPQRTPCSAQSRPGWCAGPRRRHAPGTEPHVAPGRAPPPRAGASPGSRLLPGSPSLLLPAATWRTWGQESKVLRKILKAWDPFSLL
Show »
MSGPPSAPQGALAAPRSPAVRRKGLQAPSWGSPGRPAAHSPWACGPPHWGPQRGPRNAAAARPGPRSRWHKRCAAACGACARPPGHQLQPPGAGAPQPGVACSYL
GPRPQRTPCSAQSRPGWCAGPRRRHAPGTEPHVAPGRAPPPRAGASPGSRLLPGSPSLLLPAATWRTWGQESKVLRKILKAWDPFSLL
Show »


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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (2) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |
Egger G, 2014 | Austria | Microarray | - | - | ASD | 73 | - | - | - | 245 | 2357 | - |














Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.