Evidence Details for C22orf9
Basic Information Top
| Gene Symbol: | C22orf9 ( - ) |
|---|---|
| Gene Full Name: | chromosome 22 open reading frame 9 |
| Band: | 22q13.31 |
| Quick Links | Entrez ID:23313; OMIM: NA; Uniprot ID:CV009_HUMAN; ENSEMBL ID: ENSG00000100364; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C22orf9|23313|nucleotide
ATGCTGCGTGCCATAGCGGAGGAGCGCGGCCGTCTTAGCCTGCGCCGCGAGGTCTGCGGCCTCGGGTGCTTCAAGGATGACCGCATCGTCTTCTGGACTTGGATG
TTCTCCACCTACTTCATGGAGAAATGGGCTCCCCGGCAGGACGACATGCTTTTCTATGTGCGCCGGAAGCTGGCGTACTCCGGCAGCGAAAGCGGTGCAGACGGG
AGGAAGGCAGCTGAGCCTGAGGTGGAGGTGGAGGTGTACCGGCGGGACTCCAAGAAGCTGCCAGGCCTGGGAGACCCTGACATCGACTGGGAGGAGAGCGTCTGC
CTGAATCTCATCCTGCAGAAGCTGGACTACATGGTGACCTGTGCGGTGTGCACACGTGCTGACGGCGGGGACATTCACATCCATAAGAAGAAATCTCAGCAAGTG
TTCGCGTCCCCCAGTAAACACCCCATGGACAGCAAGGGGGAGGAGTCCAAGATCAGCTACCCCAACATCTTCTTCATGATTGACAGCTTCGAGGAGGTGTTCAGC
GACATGACCGTAGGGGAAGGAGAGATGGTCTGTGTGGAGCTGGTGGCTAGTGACAAAACCAACACGTTCCAGGGGGTCATCTTTCAGGGCTCCATCCGCTACGAG
GCGCTCAAGAAGGTGTATGACAACCGGGTGAGCGTGGCCGCCCGCATGGCACAGAAGATGTCGTTTGGCTTCTACAAGTACAGCAACATGGAGTTTGTGCGCATG
AAGGGCCCCCAGGGCAAGGGCCACGCCGAGATGGCGGTCAGCCGAGTGTCTACAGGTGACACATCCCCCTGTGGGACTGAAGAGGACTCCAGCCCAGCTTCGCCC
ATGCACGAGCGGGTGACCTCCTTCAGCACACCCCCCACCCCAGAACGGAACAACCGGCCTGCCTTCTTCTCCCCATCCCTCAAGAGGAAGGTGCCCCGGAACCGG
ATCGCTGAGATGAAGAAGTCGCACTCGGCCAACGACAGCGAGGAGTTCTTCCGGGAGGACGACGGTGGAGCCGATCTGCACAATGCAACCAACCTGCGGTCTCGG
TCCCTGTCGGGCACAGGACGGTCCCTGGTCGGGTCCTGGCTGAAGCTGAACAGAGCAGATGGAAACTTCCTTCTCTATGCACACTTAACCTACGTCACGTTGCCG
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ATGCTGCGTGCCATAGCGGAGGAGCGCGGCCGTCTTAGCCTGCGCCGCGAGGTCTGCGGCCTCGGGTGCTTCAAGGATGACCGCATCGTCTTCTGGACTTGGATG
TTCTCCACCTACTTCATGGAGAAATGGGCTCCCCGGCAGGACGACATGCTTTTCTATGTGCGCCGGAAGCTGGCGTACTCCGGCAGCGAAAGCGGTGCAGACGGG
AGGAAGGCAGCTGAGCCTGAGGTGGAGGTGGAGGTGTACCGGCGGGACTCCAAGAAGCTGCCAGGCCTGGGAGACCCTGACATCGACTGGGAGGAGAGCGTCTGC
CTGAATCTCATCCTGCAGAAGCTGGACTACATGGTGACCTGTGCGGTGTGCACACGTGCTGACGGCGGGGACATTCACATCCATAAGAAGAAATCTCAGCAAGTG
TTCGCGTCCCCCAGTAAACACCCCATGGACAGCAAGGGGGAGGAGTCCAAGATCAGCTACCCCAACATCTTCTTCATGATTGACAGCTTCGAGGAGGTGTTCAGC
GACATGACCGTAGGGGAAGGAGAGATGGTCTGTGTGGAGCTGGTGGCTAGTGACAAAACCAACACGTTCCAGGGGGTCATCTTTCAGGGCTCCATCCGCTACGAG
GCGCTCAAGAAGGTGTATGACAACCGGGTGAGCGTGGCCGCCCGCATGGCACAGAAGATGTCGTTTGGCTTCTACAAGTACAGCAACATGGAGTTTGTGCGCATG
AAGGGCCCCCAGGGCAAGGGCCACGCCGAGATGGCGGTCAGCCGAGTGTCTACAGGTGACACATCCCCCTGTGGGACTGAAGAGGACTCCAGCCCAGCTTCGCCC
ATGCACGAGCGGGTGACCTCCTTCAGCACACCCCCCACCCCAGAACGGAACAACCGGCCTGCCTTCTTCTCCCCATCCCTCAAGAGGAAGGTGCCCCGGAACCGG
ATCGCTGAGATGAAGAAGTCGCACTCGGCCAACGACAGCGAGGAGTTCTTCCGGGAGGACGACGGTGGAGCCGATCTGCACAATGCAACCAACCTGCGGTCTCGG
TCCCTGTCGGGCACAGGACGGTCCCTGGTCGGGTCCTGGCTGAAGCTGAACAGAGCAGATGGAAACTTCCTTCTCTATGCACACTTAACCTACGTCACGTTGCCG
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>C22orf9|23313|protein
MLRAIAEERGRLSLRREVCGLGCFKDDRIVFWTWMFSTYFMEKWAPRQDDMLFYVRRKLAYSGSESGADGRKAAEPEVEVEVYRRDSKKLPGLGDPDIDWEESVC
LNLILQKLDYMVTCAVCTRADGGDIHIHKKKSQQVFASPSKHPMDSKGEESKISYPNIFFMIDSFEEVFSDMTVGEGEMVCVELVASDKTNTFQGVIFQGSIRYE
ALKKVYDNRVSVAARMAQKMSFGFYKYSNMEFVRMKGPQGKGHAEMAVSRVSTGDTSPCGTEEDSSPASPMHERVTSFSTPPTPERNNRPAFFSPSLKRKVPRNR
IAEMKKSHSANDSEEFFREDDGGADLHNATNLRSRSLSGTGRSLVGSWLKLNRADGNFLLYAHLTYVTLPLHRILTDILEVRQKPILMT
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MLRAIAEERGRLSLRREVCGLGCFKDDRIVFWTWMFSTYFMEKWAPRQDDMLFYVRRKLAYSGSESGADGRKAAEPEVEVEVYRRDSKKLPGLGDPDIDWEESVC
LNLILQKLDYMVTCAVCTRADGGDIHIHKKKSQQVFASPSKHPMDSKGEESKISYPNIFFMIDSFEEVFSDMTVGEGEMVCVELVASDKTNTFQGVIFQGSIRYE
ALKKVYDNRVSVAARMAQKMSFGFYKYSNMEFVRMKGPQGKGHAEMAVSRVSTGDTSPCGTEEDSSPASPMHERVTSFSTPPTPERNNRPAFFSPSLKRKVPRNR
IAEMKKSHSANDSEEFFREDDGGADLHNATNLRSRSLSGTGRSLVGSWLKLNRADGNFLLYAHLTYVTLPLHRILTDILEVRQKPILMT
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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) | 1 (4) | 0 (0) | 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 | ||||||
| Goizet, 2000 | - | FISH |  | | autism | - | - | - | - | 1 | - | 1 |
| Prasad, 2000 | - | FISH | | | autism | - | - | - | - | 1 | - | 1 |
| Wassink, 2001 | USA | Chromosomal analysis of G-band | | | autism | - | - | - | - | 278 | - | 278 |
| Chen, 2011 | - | FISH, aCGH | - | - | autism | - | - | - | - | 1 | - | 1 |
Linkage Studies TopLow 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.