Evidence Details for C3orf18
Basic Information Top
| Gene Symbol: | C3orf18 ( G20 ) |
|---|---|
| Gene Full Name: | chromosome 3 open reading frame 18 |
| Band: | 3p21.31 |
| Quick Links | Entrez ID:51161; OMIM: NA; Uniprot ID:CC018_HUMAN; ENSEMBL ID: ENSG00000088543; HGNC ID: 24837 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C3orf18|51161|nucleotide
ATGAACTCCAGGACCGCATCTGCTAGGGGCTGGTTCAGCAGCCGCCCACCCACCTCTGAGTCTGACCTGGAACCTGCCACAGATGGGCCAGCCTCCGAGACCACT
ACCCTCAGCCCAGAGGCCACCACCTTTAATGACACCAGAATCCCTGATGCAGCTGGTGGCACGGCCGGCGTGGGTACCATGCTTCTGTCCTTTGGGATCATCACG
GTGATAGGCCTGGCTGTGGCCTTGGTTTTGTACATCAGGAAGAAGAAGAGGCTGGAGAAGCTACGCCACCAGCTCATGCCCATGTACAACTTCGACCCCACGGAG
GAACAAGATGAGTTGGAGCAGGAGCTGCTGGAGCATGGGCGGGACGCCGCCTCTGTACAGGCTGCTACTTCTGTGCAGGCCATGCAGGGCAAGACTACTCTGCCC
TCCCAGGGCCCACTGCAGAGACCCAGCCGGCTGGTGTTTACCGATGTGGCCAATGCCATCCATGCGTGA
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ATGAACTCCAGGACCGCATCTGCTAGGGGCTGGTTCAGCAGCCGCCCACCCACCTCTGAGTCTGACCTGGAACCTGCCACAGATGGGCCAGCCTCCGAGACCACT
ACCCTCAGCCCAGAGGCCACCACCTTTAATGACACCAGAATCCCTGATGCAGCTGGTGGCACGGCCGGCGTGGGTACCATGCTTCTGTCCTTTGGGATCATCACG
GTGATAGGCCTGGCTGTGGCCTTGGTTTTGTACATCAGGAAGAAGAAGAGGCTGGAGAAGCTACGCCACCAGCTCATGCCCATGTACAACTTCGACCCCACGGAG
GAACAAGATGAGTTGGAGCAGGAGCTGCTGGAGCATGGGCGGGACGCCGCCTCTGTACAGGCTGCTACTTCTGTGCAGGCCATGCAGGGCAAGACTACTCTGCCC
TCCCAGGGCCCACTGCAGAGACCCAGCCGGCTGGTGTTTACCGATGTGGCCAATGCCATCCATGCGTGA
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>C3orf18|51161|protein
MNSRTASARGWFSSRPPTSESDLEPATDGPASETTTLSPEATTFNDTRIPDAAGGTAGVGTMLLSFGIITVIGLAVALVLYIRKKKRLEKLRHQLMPMYNFDPTE
EQDELEQELLEHGRDAASVQAATSVQAMQGKTTLPSQGPLQRPSRLVFTDVANAIHA
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MNSRTASARGWFSSRPPTSESDLEPATDGPASETTTLSPEATTFNDTRIPDAAGGTAGVGTMLLSFGIITVIGLAVALVLYIRKKKRLEKLRHQLMPMYNFDPTE
EQDELEQELLEHGRDAASVQAATSVQAMQGKTTLPSQGPLQRPSRLVFTDVANAIHA
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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 (0) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 1 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
| Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Voineagu, 2011_1 | Unknown | 16 frontal cortex(BA9) and 13 temporal cortex(BA41 | 16 (25.00%) | ![]() | ![]() | - | autism | 16 (6.25%) |
0.933374 | Down | 10.35 | |
| ||||||||||||
Proteomics Studies:0
| Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
|---|---|---|---|---|---|---|---|---|---|
| No Evidence. | |||||||||
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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