Evidence Details for C16orf13
Basic Information Top
| Gene Symbol: | C16orf13 ( MGC13114 ) |
|---|---|
| Gene Full Name: | chromosome 16 open reading frame 13 |
| Band: | 16p13.3 |
| Quick Links | Entrez ID:84326; OMIM: NA; Uniprot ID:CP013_HUMAN; ENSEMBL ID: ENSG00000130731,ENSG00000248465,ENSG00000249124,EN; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C16orf13|84326|nucleotide
ATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACGTGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCC
TCGGGCTCCGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTGGACCAGCGCTGCCTGGACAGCATCGCGGCCACC
ACGCAAGCCCAGGGCCTGACCAACGTGAAGGCCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCTGGACCTGTTG
CTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTCATCACCTACGGG
GAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATG
CCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAG
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ATGCTGGTGGCGGCGGCCGCGGAGCGGAACAAGGATCCCATCTTGCACGTGCTGCGGCAGTACCTGGATCCGGCCCAGCGTGGCGTCCGCGTCCTCGAGGTGGCC
TCGGGCTCCGGCCAGCACGCAGCGCACTTCGCGCGGGCCTTCCCCCTGGCCGAGTGGCAGCCGTCGGACGTGGACCAGCGCTGCCTGGACAGCATCGCGGCCACC
ACGCAAGCCCAGGGCCTGACCAACGTGAAGGCCCCGCTACACCTGGACGTGACGTGGGGCTGGGAGCACTGGGGCGGGATCCTGCCACAGTCGCTGGACCTGTTG
CTCTGCATCAACATGGCCCATGTCAGCCCCCTGCGCTGCACGGAGGGGCTCTTCAGAGCAGCAGGACACCTGCTCAAACCCAGGGCCCTGCTCATCACCTACGGG
GAACCCAGAATGGGGGCTTCGGGACACAGCCCTCCTGGAGGACCTGGGAAAGGCCAGTGGCCTGCTCCTGGAGAGGATGGTGGACATGCCAGCCAACAACAAATG
CCTGATCTTCCGGAAAAACTAAGCCCCTCCTTCACCCCCGCACACCTGCATCCCTGCCGGAGGCTCTGTGAGGCACGAACCCTGCCTCCCTAG
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>C16orf13|84326|protein
MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCLDSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLL
LCINMAHVSPLRCTEGLFRAAGHLLKPRALLITYGEPRMGASGHSPPGGPGKGQWPAPGEDGGHASQQQMPDLPEKLSPSFTPAHLHPCRRLCEARTLPP
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MLVAAAAERNKDPILHVLRQYLDPAQRGVRVLEVASGSGQHAAHFARAFPLAEWQPSDVDQRCLDSIAATTQAQGLTNVKAPLHLDVTWGWEHWGGILPQSLDLL
LCINMAHVSPLRCTEGLFRAAGHLLKPRALLITYGEPRMGASGHSPPGGPGKGQWPAPGEDGGHASQQQMPDLPEKLSPSFTPAHLHPCRRLCEARTLPP
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Evidence summary TopClick 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 (2) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (4) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
| Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Buxbaum, 2004 | USA | microsatellite-based genomic screen |  |  | autism | 115 | - | 115 | - | - | - | - |
| Lauritsen, 2006 | Faroe Islands | microsatellite-based genomic screen | | | autism | - | - | - | - | 12 | 44 | 56 |
Low Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS de novo Mutation Studies TopNGS Mosaic SNV Studies TopNGS Other Studies Top Low Scale Gene Studies TopContact 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.