Evidence Details for C22orf29
Basic Information Top
| Gene Symbol: | C22orf29 ( FLJ21125 ) |
|---|---|
| Gene Full Name: | chromosome 22 open reading frame 29 |
| Band: | 22q11.21 |
| Quick Links | Entrez ID:79680; OMIM: NA; Uniprot ID:CV029_HUMAN; ENSEMBL ID: ENSG00000215012; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C22orf29|79680|nucleotide
ATGCCTCGTGGCCGGTGCCGTCAGCAGGGCCCTCGCATTCCCATCTGGGCAGCCGCCAATTATGCCAACGCACATCCATGGCAGCAGATGGACAAGGCGTCTCCT
GGGGTGGCATACACCCCCCTTGTGGATCCCTGGATTGAGCGGCCCTGCTGTGGGGACACCGTGTGTGTGCGAACGACCATGGAGCAGAAGAGCACAGCTAGTGGC
ACTTGTGGCGGTAAACCTGCAGAAAGGGGTCCCCTAGCTGGGCACATGCCCAGCTCCCGACCCCACAGGGTGGACTTCTGCTGGGTACCAGGCTCAGACCCAGGC
ACCTTTGATGGCTCCCCGTGGCTACTGGACCGCTTCTTGGCCCAGCTGGGCGATTACATGTCCTTCCACTTTGAGCACTATCAGGACAACATCAGCCGTGTCTGC
GAGATCCTCAGGCGCCTAACAGGCCGAGCCCAGGCCTGGGCAGCCCCCTACCTTGATGGGGACCTGCCCCTGCCTGACGATTACGAGCTCTTCTGCCAGGATCTC
AAGGAAGTTGTTCAAGACCCGAACAGTTTTGCTGAGTACCATGCTGTGGTTACCTGTCCCCTGCCCCTGGCCTCCAGCCAGCTGCCAGTGGCCCCTCAGCTGCCT
GTGGTGAGGCAATACTTAGCTAGGTTCTTAGAGGGCCTGGCACTCGACATGGGTACTGCCCCCAGGTCTTTACCAGCCGCCATGGCCACCCCTGCTGTGTCTGGG
TCCAACTCTGTATCTAGAAGTGCTCTGTTCGAGCAGCAGCTGACCAAGGAGAGCACCCCTGGGCCCAAGGAGCCCCCAGTCCTGCCCAGTTCTACATGTAGCTCC
AAGCCTGGTCCTGTGGAACCAGCCTCTTCCCAGCCAGAGGAGGCAGCCCCCACACCTGTCCCTAGACTGTCGGAGTCAGCTAATCCTCCTGCCCAGAGACCAGAC
CCAGCTCATCCAGGAGGTCCAAAACCCCAGAAAACAGAGGAGGAGGTTTTGGAGACAGAGGGAGACCAGGAGGTGTCCTTAGGTACCCCACAGGAGGTGGTGGAG
GCCCCGGAGACCCCAGGAGAGCCACCACTTTCTCCTGGGTTCTGA
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ATGCCTCGTGGCCGGTGCCGTCAGCAGGGCCCTCGCATTCCCATCTGGGCAGCCGCCAATTATGCCAACGCACATCCATGGCAGCAGATGGACAAGGCGTCTCCT
GGGGTGGCATACACCCCCCTTGTGGATCCCTGGATTGAGCGGCCCTGCTGTGGGGACACCGTGTGTGTGCGAACGACCATGGAGCAGAAGAGCACAGCTAGTGGC
ACTTGTGGCGGTAAACCTGCAGAAAGGGGTCCCCTAGCTGGGCACATGCCCAGCTCCCGACCCCACAGGGTGGACTTCTGCTGGGTACCAGGCTCAGACCCAGGC
ACCTTTGATGGCTCCCCGTGGCTACTGGACCGCTTCTTGGCCCAGCTGGGCGATTACATGTCCTTCCACTTTGAGCACTATCAGGACAACATCAGCCGTGTCTGC
GAGATCCTCAGGCGCCTAACAGGCCGAGCCCAGGCCTGGGCAGCCCCCTACCTTGATGGGGACCTGCCCCTGCCTGACGATTACGAGCTCTTCTGCCAGGATCTC
AAGGAAGTTGTTCAAGACCCGAACAGTTTTGCTGAGTACCATGCTGTGGTTACCTGTCCCCTGCCCCTGGCCTCCAGCCAGCTGCCAGTGGCCCCTCAGCTGCCT
GTGGTGAGGCAATACTTAGCTAGGTTCTTAGAGGGCCTGGCACTCGACATGGGTACTGCCCCCAGGTCTTTACCAGCCGCCATGGCCACCCCTGCTGTGTCTGGG
TCCAACTCTGTATCTAGAAGTGCTCTGTTCGAGCAGCAGCTGACCAAGGAGAGCACCCCTGGGCCCAAGGAGCCCCCAGTCCTGCCCAGTTCTACATGTAGCTCC
AAGCCTGGTCCTGTGGAACCAGCCTCTTCCCAGCCAGAGGAGGCAGCCCCCACACCTGTCCCTAGACTGTCGGAGTCAGCTAATCCTCCTGCCCAGAGACCAGAC
CCAGCTCATCCAGGAGGTCCAAAACCCCAGAAAACAGAGGAGGAGGTTTTGGAGACAGAGGGAGACCAGGAGGTGTCCTTAGGTACCCCACAGGAGGTGGTGGAG
GCCCCGGAGACCCCAGGAGAGCCACCACTTTCTCCTGGGTTCTGA
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>C22orf29|79680|protein
MPRGRCRQQGPRIPIWAAANYANAHPWQQMDKASPGVAYTPLVDPWIERPCCGDTVCVRTTMEQKSTASGTCGGKPAERGPLAGHMPSSRPHRVDFCWVPGSDPG
TFDGSPWLLDRFLAQLGDYMSFHFEHYQDNISRVCEILRRLTGRAQAWAAPYLDGDLPLPDDYELFCQDLKEVVQDPNSFAEYHAVVTCPLPLASSQLPVAPQLP
VVRQYLARFLEGLALDMGTAPRSLPAAMATPAVSGSNSVSRSALFEQQLTKESTPGPKEPPVLPSSTCSSKPGPVEPASSQPEEAAPTPVPRLSESANPPAQRPD
PAHPGGPKPQKTEEEVLETEGDQEVSLGTPQEVVEAPETPGEPPLSPGF
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MPRGRCRQQGPRIPIWAAANYANAHPWQQMDKASPGVAYTPLVDPWIERPCCGDTVCVRTTMEQKSTASGTCGGKPAERGPLAGHMPSSRPHRVDFCWVPGSDPG
TFDGSPWLLDRFLAQLGDYMSFHFEHYQDNISRVCEILRRLTGRAQAWAAPYLDGDLPLPDDYELFCQDLKEVVQDPNSFAEYHAVVTCPLPLASSQLPVAPQLP
VVRQYLARFLEGLALDMGTAPRSLPAAMATPAVSGSNSVSRSALFEQQLTKESTPGPKEPPVLPSSTCSSKPGPVEPASSQPEEAAPTPVPRLSESANPPAQRPD
PAHPGGPKPQKTEEEVLETEGDQEVSLGTPQEVVEAPETPGEPPLSPGF
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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) | 2 (11) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 6 (12) |
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 | ||||||
| Roubertie, 2001 | - | FISH |  | | autism | - | - | - | - | 1 | - | 1 |
| Niklasson, 2002 | Sweden | FISH | | | autism | - | - | - | - | 1 | - | 1 |
| Szatmari, 2007 | Europe, North America | SNP microarray |  | | ASD | 1491 | - | - | - | - | - | 0 |
| Christian, 2008 | USA | aCGH | | | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 |
| Ramelli, 2008 | - | FISH | | | ASD | - | - | - | - | 1 | - | 1 |
| Marshall, 2008 | - | SNP microarray | | | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 |
| Bucan, 2009 | USA | SNP microarray | | | autism, ASD | 912 | - | 912 | - | - | 1488 | 1488 |
| Pinto, 2010 | - | SNP microarray, qPCR | | | ASD | - | - | - | - | 996 | 1287 | 2283 |
| Bremer, 2011 | - | aCGH | | | ASD | - | - | - | - | 223 | - | 223 |
| 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 | ||||||
| Bailey, 1998 | - | microsatellite-based genomic screen | | | PDD | 99 | - | 99 | - | - | - | - |
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.