Evidence Details for C15orf32
Basic Information Top
| Gene Symbol: | C15orf32 ( FLJ32831,MGC129836,MGC129837 ) |
|---|---|
| Gene Full Name: | chromosome 15 open reading frame 32 |
| Band: | 15q26.1 |
| Quick Links | Entrez ID:145858; OMIM: NA; Uniprot ID:CO032_HUMAN; ENSEMBL ID: ENSG00000183643; HGNC ID: 26549 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C15orf32|145858|nucleotide
ATGAACAAAAGAACAAGTGTGGATGCTTCAAAGGAAGACTTGCACCCGGCTGACCCCCAGAGTGGGGAAGGGGTCCCACCTAATAGGAAGAACACCAAGACTTCC
CCAAGAGGAGAAGGAACGGCTCCCCCTTTCTCGGCGAGGCCATGTGTCTGGACCCTGTGTGAGATGCTTTCTATACTAGCCCTTGTTGGGGTGTTGCACCCATTT
TACAGATCAAACAACCAAGTTTATCAGAAATTAAAGACTCATTTAAGATGCCAAAGCTCACGAGTGGATGGTTTGATGCTGAAGCCAACATTGTTAACACCATCT
CAGCTCAAAAGCCCTGAAGGCCACTTAATTCTACCAACCTTCAACCATCTTGTCATAAGACACATCCTCGACCCAAAGCAGATATTCTGTGTAGCTGATGTGTGT
ACAGATTGCAAATTCAATTGCGGAAGCATAGAGAGGCACCAGAAGAGGCATCTTATGAGAGTCAGCCAGGACTGGGAACATTTAATAAGATACAGAAACCAGATT
TGCTTGAGCTGA
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ATGAACAAAAGAACAAGTGTGGATGCTTCAAAGGAAGACTTGCACCCGGCTGACCCCCAGAGTGGGGAAGGGGTCCCACCTAATAGGAAGAACACCAAGACTTCC
CCAAGAGGAGAAGGAACGGCTCCCCCTTTCTCGGCGAGGCCATGTGTCTGGACCCTGTGTGAGATGCTTTCTATACTAGCCCTTGTTGGGGTGTTGCACCCATTT
TACAGATCAAACAACCAAGTTTATCAGAAATTAAAGACTCATTTAAGATGCCAAAGCTCACGAGTGGATGGTTTGATGCTGAAGCCAACATTGTTAACACCATCT
CAGCTCAAAAGCCCTGAAGGCCACTTAATTCTACCAACCTTCAACCATCTTGTCATAAGACACATCCTCGACCCAAAGCAGATATTCTGTGTAGCTGATGTGTGT
ACAGATTGCAAATTCAATTGCGGAAGCATAGAGAGGCACCAGAAGAGGCATCTTATGAGAGTCAGCCAGGACTGGGAACATTTAATAAGATACAGAAACCAGATT
TGCTTGAGCTGA
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>C15orf32|145858|protein
MNKRTSVDASKEDLHPADPQSGEGVPPNRKNTKTSPRGEGTAPPFSARPCVWTLCEMLSILALVGVLHPFYRSNNQVYQKLKTHLRCQSSRVDGLMLKPTLLTPS
QLKSPEGHLILPTFNHLVIRHILDPKQIFCVADVCTDCKFNCGSIERHQKRHLMRVSQDWEHLIRYRNQICLS
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MNKRTSVDASKEDLHPADPQSGEGVPPNRKNTKTSPRGEGTAPPFSARPCVWTLCEMLSILALVGVLHPFYRSNNQVYQKLKTHLRCQSSRVDGLMLKPTLLTPS
QLKSPEGHLILPTFNHLVIRHILDPKQIFCVADVCTDCKFNCGSIERHQKRHLMRVSQDWEHLIRYRNQICLS
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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 (3) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 4 (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 | ||||||
| Bonati, 2005 | - | FISH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Szatmari, 2007 | Europe, North America | SNP microarray | ![]() | ![]() | ASD | 1491 | - | - | - | - | - | 0 |
| Kamien B, 2014 | - | aCGH | ![]() | ![]() | autism | 1 | - | - | - | 1 | - | 1 |
Linkage Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Risch, 1999 | USA | microsatellite-based genomic screen | ![]() | ![]() | PDD | 90 | - | 90 | - | - | - | - |
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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