Evidence Details for C9orf172
Basic Information Top
| Gene Symbol: | C9orf172 ( - ) |
|---|---|
| Gene Full Name: | chromosome 9 open reading frame 172 |
| Band: | 9q34.3 |
| Quick Links | Entrez ID:389813; OMIM: NA; Uniprot ID:CI172_HUMAN; ENSEMBL ID: ENSG00000232434; HGNC ID: 37284 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C9orf172|389813|nucleotide
ATGACCCGTACGGACCCTCCGGACCTGCTGGTGTCGACCGTGTACCAGGACATCAAGGTGGCGACCCCGGGACCCGCGTCCAAGTGCTCGCCATGTGAGCGATCC
GTGGCCCGGCCTGCTGAGCCCGCGCCTTTCAACAAGCGCCACTGCCGCAGCTTCGACTTCCTGGAGGCGCTGGACGGGCCGGCCATGGAGACCCTGCCGGAGCCA
CCGCCGCCGGAGTCCGCTGTGCCGCGCGCCCGGACCCGCGAAGCCGAGCCACGCCGCCGCGCCCGCTCCAAGAGTGCGCCCCGCGCGCCCCCGGGCCTGACGCCC
GCGCCCGCCTCGCCGCCGGTGTTGCCCCGCCGAGGGCGGGAGGCCCAGCGTGCGGCGCGGGCCGAGGCATCGCCGCGCCGGGAGCCCGCGTACCCGGCGCTCCGC
GCCCTTGCCAACGAGCTGCATCCCATCAAGTTGCAGCCGCAGCGGGGCGGCCCCGGCCGCGTCGCGCCCCTGTGCGCCGCCGCGGGCCGCTGCGCACCGCCCGAG
CCACCCGCGGGTCCCGCCCCCCACGTGCGCTGCCGCCTGGACATCAAGCCAGACGACGCAGTGCTCCAGCACGCCACCCGGGGCTCGCGGTCCTGCGGGCCCACC
GAGGCCGCGCACTGGGCCCGCCCCGCCCCGCAGTTCCACGGCCTCACGGTGCCCGGGCCCCGCCACATGGCGCTGTCGCGCACCCCGACGCCCAGCGACTCATAC
TGTGCGGATCCCCGGGCGTTCTACTGCGACGGGCCCCTGCCTGGGCCCCGGGACTACGCCGAGCGCCGCAGTCTGCCCTTCACCACCCCGCCGGGCCCCACCCAG
TTCTTCTATACAGAGGAGCCCCAAGGCTTCCGGGGCAGCTTTGCAGCCAGTCCCGGCCCAACCTTCGACGCCTACTACCCCAGGCCCTATCCGTCCGAGGAGCTC
TCGGGGCCCAGTCCAAGGCGCATGGGCGGCTACTACGCAGGAGAGGTGCGCACCTTCCCAATCCAGGAACCGCCCTCCCGCTCCTACTATGGGGAGGCTCCACGA
GCCTACGGCCTGCCCTACGGGCCCCGCTATGTCCCCGAGGAGCCCCGGGCCCACTCCACCGCCCGCCCCTTTTACACGGAGGACTTCGGAAGGTACCGCGAGCGT
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ATGACCCGTACGGACCCTCCGGACCTGCTGGTGTCGACCGTGTACCAGGACATCAAGGTGGCGACCCCGGGACCCGCGTCCAAGTGCTCGCCATGTGAGCGATCC
GTGGCCCGGCCTGCTGAGCCCGCGCCTTTCAACAAGCGCCACTGCCGCAGCTTCGACTTCCTGGAGGCGCTGGACGGGCCGGCCATGGAGACCCTGCCGGAGCCA
CCGCCGCCGGAGTCCGCTGTGCCGCGCGCCCGGACCCGCGAAGCCGAGCCACGCCGCCGCGCCCGCTCCAAGAGTGCGCCCCGCGCGCCCCCGGGCCTGACGCCC
GCGCCCGCCTCGCCGCCGGTGTTGCCCCGCCGAGGGCGGGAGGCCCAGCGTGCGGCGCGGGCCGAGGCATCGCCGCGCCGGGAGCCCGCGTACCCGGCGCTCCGC
GCCCTTGCCAACGAGCTGCATCCCATCAAGTTGCAGCCGCAGCGGGGCGGCCCCGGCCGCGTCGCGCCCCTGTGCGCCGCCGCGGGCCGCTGCGCACCGCCCGAG
CCACCCGCGGGTCCCGCCCCCCACGTGCGCTGCCGCCTGGACATCAAGCCAGACGACGCAGTGCTCCAGCACGCCACCCGGGGCTCGCGGTCCTGCGGGCCCACC
GAGGCCGCGCACTGGGCCCGCCCCGCCCCGCAGTTCCACGGCCTCACGGTGCCCGGGCCCCGCCACATGGCGCTGTCGCGCACCCCGACGCCCAGCGACTCATAC
TGTGCGGATCCCCGGGCGTTCTACTGCGACGGGCCCCTGCCTGGGCCCCGGGACTACGCCGAGCGCCGCAGTCTGCCCTTCACCACCCCGCCGGGCCCCACCCAG
TTCTTCTATACAGAGGAGCCCCAAGGCTTCCGGGGCAGCTTTGCAGCCAGTCCCGGCCCAACCTTCGACGCCTACTACCCCAGGCCCTATCCGTCCGAGGAGCTC
TCGGGGCCCAGTCCAAGGCGCATGGGCGGCTACTACGCAGGAGAGGTGCGCACCTTCCCAATCCAGGAACCGCCCTCCCGCTCCTACTATGGGGAGGCTCCACGA
GCCTACGGCCTGCCCTACGGGCCCCGCTATGTCCCCGAGGAGCCCCGGGCCCACTCCACCGCCCGCCCCTTTTACACGGAGGACTTCGGAAGGTACCGCGAGCGT
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>C9orf172|389813|protein
MTRTDPPDLLVSTVYQDIKVATPGPASKCSPCERSVARPAEPAPFNKRHCRSFDFLEALDGPAMETLPEPPPPESAVPRARTREAEPRRRARSKSAPRAPPGLTP
APASPPVLPRRGREAQRAARAEASPRREPAYPALRALANELHPIKLQPQRGGPGRVAPLCAAAGRCAPPEPPAGPAPHVRCRLDIKPDDAVLQHATRGSRSCGPT
EAAHWARPAPQFHGLTVPGPRHMALSRTPTPSDSYCADPRAFYCDGPLPGPRDYAERRSLPFTTPPGPTQFFYTEEPQGFRGSFAASPGPTFDAYYPRPYPSEEL
SGPSPRRMGGYYAGEVRTFPIQEPPSRSYYGEAPRAYGLPYGPRYVPEEPRAHSTARPFYTEDFGRYRERDVLARTYPHPRSSPAWADWGPRPYRTLQVVPPSDP
DPLLASWHGGTGTSPPRLATDSRHYSRSWDNILAPGPRREDPLGRGRSYENLLGREVREPRGVSPEGRRPPVVVNLSTSPRRYAALSLSETSLTEKGRAGEGLGR
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MTRTDPPDLLVSTVYQDIKVATPGPASKCSPCERSVARPAEPAPFNKRHCRSFDFLEALDGPAMETLPEPPPPESAVPRARTREAEPRRRARSKSAPRAPPGLTP
APASPPVLPRRGREAQRAARAEASPRREPAYPALRALANELHPIKLQPQRGGPGRVAPLCAAAGRCAPPEPPAGPAPHVRCRLDIKPDDAVLQHATRGSRSCGPT
EAAHWARPAPQFHGLTVPGPRHMALSRTPTPSDSYCADPRAFYCDGPLPGPRDYAERRSLPFTTPPGPTQFFYTEEPQGFRGSFAASPGPTFDAYYPRPYPSEEL
SGPSPRRMGGYYAGEVRTFPIQEPPSRSYYGEAPRAYGLPYGPRYVPEEPRAHSTARPFYTEDFGRYRERDVLARTYPHPRSSPAWADWGPRPYRTLQVVPPSDP
DPLLASWHGGTGTSPPRLATDSRHYSRSWDNILAPGPRREDPLGRGRSYENLLGREVREPRGVSPEGRRPPVVVNLSTSPRRYAALSLSETSLTEKGRAGEGLGR
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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 (3) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (5) |
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 | ||||||
| Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |
| Pinto, 2010 | - | SNP microarray, qPCR | ![]() | ![]() | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Monaco, 2001 | - | microsatellite-based genomic screen | ![]() | ![]() | PDD | 152 | - | 152 | - | - | - | - |
| Buxbaum, 2001 | USA | microsatellite-based genomic screen | ![]() | ![]() | autism, PDD, Asperger syndrome | 35 | - | 35 | - | - | - | - |
| Lamb, 2005 | - | microsatellite-based genomic screen | ![]() | ![]() | autism | 207 | - | 207 | - | 420 | - | - |
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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