Evidence Details for C15orf62
Basic Information Top
Gene Symbol: | C15orf62 ( - ) |
---|---|
Gene Full Name: | chromosome 15 open reading frame 62 |
Band: | 15q15.1 |
Quick Links | Entrez ID:643338; OMIM: NA; Uniprot ID:CO062_HUMAN; ENSEMBL ID: ENSG00000188277; HGNC ID: 34489 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C15orf62|643338|nucleotide
ATGGAGACCTGGCGGAAAGGCTCCTTCCGCAACGCCTCCTTCTTCAAGCAGCTGAGCCTGGGGCGGCCACGGCGGCTCCGGCGACAGAGTAGTGTGCTTAGCCAG
GCCAGCACAGCAGGTGGGGACCACGAGGAGTACAGCAACCGAGAAGTCATCCGGGAGCTACAAGGGAGGCCAGATGGCCGGCGCCTGCCACTGTGGGGGGACGAG
CAGCCCCGGGCCACCCTGCTGGCCCCACCCAAGCCCCCACGCCTCTACCGAGAGAGCTCAAGCTGCCCCAACATCCTGGAGCCCCCACCTGCCTACACAGCAGCC
TACTCTGCCACCCTGCCATCGGCGCTCTCTCTGTCGAGTGCCCTCCACCAGCACTCAGAGAAGGGCCTTGTGGACACTCCCTGCTTCCAGAGGACACCTACCCCA
GACCTCAGTGATCCCTTCCTCTCCTTCAAAGTGGACCTGGGGATTTCACTTCTTGAGGAAGTTCTGCAGATGCTAAGGGAGCAGTTTCCTAGCGAGCCCAGCTTC
TAA
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ATGGAGACCTGGCGGAAAGGCTCCTTCCGCAACGCCTCCTTCTTCAAGCAGCTGAGCCTGGGGCGGCCACGGCGGCTCCGGCGACAGAGTAGTGTGCTTAGCCAG
GCCAGCACAGCAGGTGGGGACCACGAGGAGTACAGCAACCGAGAAGTCATCCGGGAGCTACAAGGGAGGCCAGATGGCCGGCGCCTGCCACTGTGGGGGGACGAG
CAGCCCCGGGCCACCCTGCTGGCCCCACCCAAGCCCCCACGCCTCTACCGAGAGAGCTCAAGCTGCCCCAACATCCTGGAGCCCCCACCTGCCTACACAGCAGCC
TACTCTGCCACCCTGCCATCGGCGCTCTCTCTGTCGAGTGCCCTCCACCAGCACTCAGAGAAGGGCCTTGTGGACACTCCCTGCTTCCAGAGGACACCTACCCCA
GACCTCAGTGATCCCTTCCTCTCCTTCAAAGTGGACCTGGGGATTTCACTTCTTGAGGAAGTTCTGCAGATGCTAAGGGAGCAGTTTCCTAGCGAGCCCAGCTTC
TAA
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>C15orf62|643338|protein
METWRKGSFRNASFFKQLSLGRPRRLRRQSSVLSQASTAGGDHEEYSNREVIRELQGRPDGRRLPLWGDEQPRATLLAPPKPPRLYRESSSCPNILEPPPAYTAA
YSATLPSALSLSSALHQHSEKGLVDTPCFQRTPTPDLSDPFLSFKVDLGISLLEEVLQMLREQFPSEPSF
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METWRKGSFRNASFFKQLSLGRPRRLRRQSSVLSQASTAGGDHEEYSNREVIRELQGRPDGRRLPLWGDEQPRATLLAPPKPPRLYRESSSCPNILEPPPAYTAA
YSATLPSALSLSSALHQHSEKGLVDTPCFQRTPTPDLSDPFLSFKVDLGISLLEEVLQMLREQFPSEPSF
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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 (1) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 4 (3) |
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 | ||||||
Bucan, 2009 | USA | SNP microarray | autism, ASD | 912 | - | 912 | - | - | 1488 | 1488 |
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Allen-Brady, 2010 | USA | SNP-based genomic screen | ASD | 40 | - | 40 | - | 192 | 461 | 653 |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
O'Roak BJ, 2012 | 1703 | 209 | 242 | Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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