Evidence Details for C17orf65
Basic Information Top
| 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 |
Sequences Top
>C17orf65|339201|nucleotide
ATGTCAGGGCCTCCCAGCGCACCTCAGGGCGCACTGGCTGCGCCCCGTAGTCCAGCAGTGCGGCGAAAAGGACTTCAGGCTCCCAGTTGGGGGAGTCCTGGACGG
CCTGCAGCGCACAGTCCATGGGCGTGTGGCCCGCCCCATTGGGGACCTCAGCGCGGGCCCCGTAACGCAGCAGCAGCTCGGCCAGGCCCCCGCAGCCGTTGGCAC
AAGCGTTGTGCAGCGGCGTGTGGCGCTTGCGCCCGGCCGCCCGGGCATCAGCTCCAGCCTCCAGGAGCCGGCGCGCCGCAGCCTGGTGTCGCCTGCAGCTACCTG
GGCCCTCGGCCCCAGCGCACGCCGTGTTCAGCGCAGTCTCGCCCTGGCTGGTGCGCAGGCCCACGTCGGCGCCATGCTCCAGGTACAGAGCCACATGTTGCTCCA
GGCCGCGCGCCGCCGCCACGTGCAGGGGCGTCTCCTGGCTCTCGCCTGCTGCCAGGTTCACCGTCGCTCCTGCTTCCAGCAGCAACTTGGCGCACCTGGGGACAA
GAGAGCAAGGTCCTGAGGAAAATCCTGAAGGCTTGGGACCCCTTCAGCTTGCTGTGA
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ATGTCAGGGCCTCCCAGCGCACCTCAGGGCGCACTGGCTGCGCCCCGTAGTCCAGCAGTGCGGCGAAAAGGACTTCAGGCTCCCAGTTGGGGGAGTCCTGGACGG
CCTGCAGCGCACAGTCCATGGGCGTGTGGCCCGCCCCATTGGGGACCTCAGCGCGGGCCCCGTAACGCAGCAGCAGCTCGGCCAGGCCCCCGCAGCCGTTGGCAC
AAGCGTTGTGCAGCGGCGTGTGGCGCTTGCGCCCGGCCGCCCGGGCATCAGCTCCAGCCTCCAGGAGCCGGCGCGCCGCAGCCTGGTGTCGCCTGCAGCTACCTG
GGCCCTCGGCCCCAGCGCACGCCGTGTTCAGCGCAGTCTCGCCCTGGCTGGTGCGCAGGCCCACGTCGGCGCCATGCTCCAGGTACAGAGCCACATGTTGCTCCA
GGCCGCGCGCCGCCGCCACGTGCAGGGGCGTCTCCTGGCTCTCGCCTGCTGCCAGGTTCACCGTCGCTCCTGCTTCCAGCAGCAACTTGGCGCACCTGGGGACAA
GAGAGCAAGGTCCTGAGGAAAATCCTGAAGGCTTGGGACCCCTTCAGCTTGCTGTGA
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>C17orf65|339201|protein
MSGPPSAPQGALAAPRSPAVRRKGLQAPSWGSPGRPAAHSPWACGPPHWGPQRGPRNAAAARPGPRSRWHKRCAAACGACARPPGHQLQPPGAGAPQPGVACSYL
GPRPQRTPCSAQSRPGWCAGPRRRHAPGTEPHVAPGRAPPPRAGASPGSRLLPGSPSLLLPAATWRTWGQESKVLRKILKAWDPFSLL
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MSGPPSAPQGALAAPRSPAVRRKGLQAPSWGSPGRPAAHSPWACGPPHWGPQRGPRNAAAARPGPRSRWHKRCAAACGACARPPGHQLQPPGAGAPQPGVACSYL
GPRPQRTPCSAQSRPGWCAGPRRRHAPGTEPHVAPGRAPPPRAGASPGSRLLPGSPSLLLPAATWRTWGQESKVLRKILKAWDPFSLL
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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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 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 | ||||||
| Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |
| Egger G, 2014 | Austria | Microarray | - | - | ASD | 73 | - | - | - | 245 | 2357 | - |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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