Evidence Details for C16orf11
Basic Information Top
| Gene Symbol: | C16orf11 ( - ) |
|---|---|
| Gene Full Name: | chromosome 16 open reading frame 11 |
| Band: | 16p13.3 |
| Quick Links | Entrez ID:146325; OMIM: NA; Uniprot ID:CP011_HUMAN; ENSEMBL ID: ENSG00000161992; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C16orf11|146325|nucleotide
ATGTCGCGGGAGGCGGGCTCATGCCGCGTGGGCACAGGGGCGAGGGCGCGGTCTCGGAAGCCCAAGAAGCCACACTACATCCCGCGGCCCTGGGGCAAACCCTAC
AACTACAAATGCTTCCAGTGCCCCTTCACCTGCCTGGAGAAGTCACACCTCTACAACCACATGAAGTACAGCCTCTGCAAGGACTCCCTGTCCCTGCTGCTAGAC
TCCCCAGACTGGGCGTGCCGCCGTGGCTCCACCACGCCTAGGCCCCACGCACCCACCCCAGACCGCCCTGGGGAGTCCGACCCCGGCAGGCAACCCCAGGGAGCA
CGGCCCACAGGTGCTGCCCCCGCGCCTGACCTCGTGGTCGCCGACATCCACTCCCTGCACTGTGGCGGAGGCCCCAAGTCCAGGGCCAAGGGGTCCCCAGGGCCA
CCACCCCCTGTGGCTAGGGCCACCCGGAAGGGTCCCGGCCCCAGTGGGCTCCTGCCTGAGTCGTGGAAGCCGGGGATGGGAGGGGACCCAAGGGGCGTGGGTGCG
GGGGACATGGCCTCAGCAGGCCCTGAGGGCAGCGTCCCCTGCTATCCCCCGCCTGCCCCAGGGGAGTTCCCTGAGGCCCACAGCCTCCACCTGTCTCTGCTGGGC
GTCAACTACCCGCTCAGCCCCGGCCTCTTCTCCTACTTGGGGCCCTCACTGGCCGCTGCAGCCCATGTGCCCTTCCTGGCCTCGGCCAGCCCCCTGCTGCCCCCG
GCCACGGCCTTCCCAGCCGTGCAGCCCCCTCAGCGCCCCACCCCGGCCCCCCGCCTGTACTACCCGCTGCTTCTGGAGCACACTCTGGGGCTGCCAGCAGGCAAA
GCTGCCCTTGCCAAGGCCCCTGTCTCCCCCAGGAGCCCCTCTGGGACTCCGGCTCCTGGCCTGCTGAAGGTGCCAGTTCCAGGGCTGGGGCCCTGGCCCCGAGTC
ACCCCCAGGGACCCAGGGCAGGAGGGGGAGCTGGAGCGGGCAGCCCAGAGTGACCCCAGGAGGAGGCTGTCCCTGGGAAGCAGGCTGGAGCTTCCGAAGGCATCC
CCCAGCCTGACAAGGTTCTGTTCCCGGAGCAGCCTGCCCACCGGCTCCTCTGTGATGCTGTGGCCTGAGGACGGGGATCCAGGCGGCCCTGAGACCCCCGGCCCT
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ATGTCGCGGGAGGCGGGCTCATGCCGCGTGGGCACAGGGGCGAGGGCGCGGTCTCGGAAGCCCAAGAAGCCACACTACATCCCGCGGCCCTGGGGCAAACCCTAC
AACTACAAATGCTTCCAGTGCCCCTTCACCTGCCTGGAGAAGTCACACCTCTACAACCACATGAAGTACAGCCTCTGCAAGGACTCCCTGTCCCTGCTGCTAGAC
TCCCCAGACTGGGCGTGCCGCCGTGGCTCCACCACGCCTAGGCCCCACGCACCCACCCCAGACCGCCCTGGGGAGTCCGACCCCGGCAGGCAACCCCAGGGAGCA
CGGCCCACAGGTGCTGCCCCCGCGCCTGACCTCGTGGTCGCCGACATCCACTCCCTGCACTGTGGCGGAGGCCCCAAGTCCAGGGCCAAGGGGTCCCCAGGGCCA
CCACCCCCTGTGGCTAGGGCCACCCGGAAGGGTCCCGGCCCCAGTGGGCTCCTGCCTGAGTCGTGGAAGCCGGGGATGGGAGGGGACCCAAGGGGCGTGGGTGCG
GGGGACATGGCCTCAGCAGGCCCTGAGGGCAGCGTCCCCTGCTATCCCCCGCCTGCCCCAGGGGAGTTCCCTGAGGCCCACAGCCTCCACCTGTCTCTGCTGGGC
GTCAACTACCCGCTCAGCCCCGGCCTCTTCTCCTACTTGGGGCCCTCACTGGCCGCTGCAGCCCATGTGCCCTTCCTGGCCTCGGCCAGCCCCCTGCTGCCCCCG
GCCACGGCCTTCCCAGCCGTGCAGCCCCCTCAGCGCCCCACCCCGGCCCCCCGCCTGTACTACCCGCTGCTTCTGGAGCACACTCTGGGGCTGCCAGCAGGCAAA
GCTGCCCTTGCCAAGGCCCCTGTCTCCCCCAGGAGCCCCTCTGGGACTCCGGCTCCTGGCCTGCTGAAGGTGCCAGTTCCAGGGCTGGGGCCCTGGCCCCGAGTC
ACCCCCAGGGACCCAGGGCAGGAGGGGGAGCTGGAGCGGGCAGCCCAGAGTGACCCCAGGAGGAGGCTGTCCCTGGGAAGCAGGCTGGAGCTTCCGAAGGCATCC
CCCAGCCTGACAAGGTTCTGTTCCCGGAGCAGCCTGCCCACCGGCTCCTCTGTGATGCTGTGGCCTGAGGACGGGGATCCAGGCGGCCCTGAGACCCCCGGCCCT
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>C16orf11|146325|protein
MSREAGSCRVGTGARARSRKPKKPHYIPRPWGKPYNYKCFQCPFTCLEKSHLYNHMKYSLCKDSLSLLLDSPDWACRRGSTTPRPHAPTPDRPGESDPGRQPQGA
RPTGAAPAPDLVVADIHSLHCGGGPKSRAKGSPGPPPPVARATRKGPGPSGLLPESWKPGMGGDPRGVGAGDMASAGPEGSVPCYPPPAPGEFPEAHSLHLSLLG
VNYPLSPGLFSYLGPSLAAAAHVPFLASASPLLPPATAFPAVQPPQRPTPAPRLYYPLLLEHTLGLPAGKAALAKAPVSPRSPSGTPAPGLLKVPVPGLGPWPRV
TPRDPGQEGELERAAQSDPRRRLSLGSRLELPKASPSLTRFCSRSSLPTGSSVMLWPEDGDPGGPETPGPEGPLPLQPRGPVPGSPEHVGEDLTRALGDYARVEQ
RLGQLGPAGGLAPRPLREQLGKIRLELLTIHQALEQAVRPPDAPLDLSVKRAPAKGPQALGEAWGRPELGPVLTGGTPEPPGMLGPAAPQPFSGHTTKCEADSSV
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MSREAGSCRVGTGARARSRKPKKPHYIPRPWGKPYNYKCFQCPFTCLEKSHLYNHMKYSLCKDSLSLLLDSPDWACRRGSTTPRPHAPTPDRPGESDPGRQPQGA
RPTGAAPAPDLVVADIHSLHCGGGPKSRAKGSPGPPPPVARATRKGPGPSGLLPESWKPGMGGDPRGVGAGDMASAGPEGSVPCYPPPAPGEFPEAHSLHLSLLG
VNYPLSPGLFSYLGPSLAAAAHVPFLASASPLLPPATAFPAVQPPQRPTPAPRLYYPLLLEHTLGLPAGKAALAKAPVSPRSPSGTPAPGLLKVPVPGLGPWPRV
TPRDPGQEGELERAAQSDPRRRLSLGSRLELPKASPSLTRFCSRSSLPTGSSVMLWPEDGDPGGPETPGPEGPLPLQPRGPVPGSPEHVGEDLTRALGDYARVEQ
RLGQLGPAGGLAPRPLREQLGKIRLELLTIHQALEQAVRPPDAPLDLSVKRAPAKGPQALGEAWGRPELGPVLTGGTPEPPGMLGPAAPQPFSGHTTKCEADSSV
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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 (2) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (4) |
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 | ||||||
| Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
| Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top

