Evidence Details for C9orf140
 Basic Information Top
| Gene Symbol: | C9orf140 ( p42.3 ) | 
|---|---|
| Gene Full Name: | chromosome 9 open reading frame 140 | 
| Band: | 9q34.3 | 
| Quick Links | Entrez ID:89958; OMIM: 612057; Uniprot ID:CI140_HUMAN; ENSEMBL ID: ENSG00000186193; HGNC ID: | 
| Relate to Another Database: | SFARIGene; denovo-db | 
 Sequences Top
>C9orf140|89958|nucleotide
ATGGCCGGGGCCGCCATGGCCGAGCGGGGCCGCGTGCCTCCCCCCGCACCCGCGCCCAGCACGGAGGGGCTGCCGCGCGCCTTCCTGCAGAGCCTGCGCACCCTG
TTCGACATCCTGGACGACCGGCGGCGCGGCTGCGTGCACCTGCGCGAGATCGAGTCCCGCTGGCAGGGCACCGACGCGCGGGAGCTGCCCCGCGGGGTGCTGGAG
GGCTTGCGCCAGGTGGCCCCGGCCAGCGGCTACCTGACCTTCGAGCGCTTCGTGGCCGGCCTGCGCACCTCCCTGCTGAGCGCCGACGGCGGCCCCCGGGACCCC
ACGCGCGCCCCGGCCCGGCCCGGGGATCAGCCGCCGCCGCCGCCGCAGCGCCTGGTGTTCGCTCCGGCCGACGAGCCGCGGACGGTCCTGGAGAGGAAGCCCCTG
CCCCTGGGCGTGCGCGCCCCTCTGGCCGGTCCCAGCGCCGCCGCCCGCAGCCCGGAGCAGCTGTGCGCCCCGGCTGAGGCGGCGCCCTGCCCCGCGGAGCCCGAG
CGGTCCCAGAGCGCGGCGCTGGAACCGAGCTCCAGCGCGGACGCAGGTGCAGTGGCGTGCAGGGCCCTGGAGGCGGACTCAGGGGATGCCCGGCGGGCTCCCCGT
GCCCGAGGGGAACGTCGGAGGCACACCATCGCCAGCGGCGTGGACTGCGGCCTGCTGAAGCAGATGAAGGAGCTGGAGCAGGAGAAGGAGGTGCTGCTGCAGGGT
TTGGAGATGATGGCGCGGGGCCGCGACTGGTACCAGCAGCAGCTGCAACGAGTGCAGGAGCGCCAGCGCCGCCTGGGCCAGAGCAGAGCCAGCGCCGACTTTGGG
GCTGCAGGGAGCCCCCGCCCACTGGGGCGGCTACTGCCCAAGGTACAAGAGGTGGCCCGGTGCCTGGGGGAGCTGCTGGCTGCAGCCTGTGCCAGCCGGGCCCTG
CCCCCGTCCTCCTCCGGGCCCCCCTGCCCTGCCCTGACGTCCACCTCACCCCCGGTCTGGCAGCAGCAGACCATCCTCATGCTGAAGGAGCAGAACCGACTCCTC
ACCCAGGAGGTGACCGAGAAGAGTGAGCGCATCACGCAGCTGGAGCAGGAGAAGTCGGCGCTCATTAAGCAGCTGTTTGAGGCCCGCGCCCTGAGCCAGCAGGAC
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ATGGCCGGGGCCGCCATGGCCGAGCGGGGCCGCGTGCCTCCCCCCGCACCCGCGCCCAGCACGGAGGGGCTGCCGCGCGCCTTCCTGCAGAGCCTGCGCACCCTG
TTCGACATCCTGGACGACCGGCGGCGCGGCTGCGTGCACCTGCGCGAGATCGAGTCCCGCTGGCAGGGCACCGACGCGCGGGAGCTGCCCCGCGGGGTGCTGGAG
GGCTTGCGCCAGGTGGCCCCGGCCAGCGGCTACCTGACCTTCGAGCGCTTCGTGGCCGGCCTGCGCACCTCCCTGCTGAGCGCCGACGGCGGCCCCCGGGACCCC
ACGCGCGCCCCGGCCCGGCCCGGGGATCAGCCGCCGCCGCCGCCGCAGCGCCTGGTGTTCGCTCCGGCCGACGAGCCGCGGACGGTCCTGGAGAGGAAGCCCCTG
CCCCTGGGCGTGCGCGCCCCTCTGGCCGGTCCCAGCGCCGCCGCCCGCAGCCCGGAGCAGCTGTGCGCCCCGGCTGAGGCGGCGCCCTGCCCCGCGGAGCCCGAG
CGGTCCCAGAGCGCGGCGCTGGAACCGAGCTCCAGCGCGGACGCAGGTGCAGTGGCGTGCAGGGCCCTGGAGGCGGACTCAGGGGATGCCCGGCGGGCTCCCCGT
GCCCGAGGGGAACGTCGGAGGCACACCATCGCCAGCGGCGTGGACTGCGGCCTGCTGAAGCAGATGAAGGAGCTGGAGCAGGAGAAGGAGGTGCTGCTGCAGGGT
TTGGAGATGATGGCGCGGGGCCGCGACTGGTACCAGCAGCAGCTGCAACGAGTGCAGGAGCGCCAGCGCCGCCTGGGCCAGAGCAGAGCCAGCGCCGACTTTGGG
GCTGCAGGGAGCCCCCGCCCACTGGGGCGGCTACTGCCCAAGGTACAAGAGGTGGCCCGGTGCCTGGGGGAGCTGCTGGCTGCAGCCTGTGCCAGCCGGGCCCTG
CCCCCGTCCTCCTCCGGGCCCCCCTGCCCTGCCCTGACGTCCACCTCACCCCCGGTCTGGCAGCAGCAGACCATCCTCATGCTGAAGGAGCAGAACCGACTCCTC
ACCCAGGAGGTGACCGAGAAGAGTGAGCGCATCACGCAGCTGGAGCAGGAGAAGTCGGCGCTCATTAAGCAGCTGTTTGAGGCCCGCGCCCTGAGCCAGCAGGAC
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>C9orf140|89958|protein
MAGAAMAERGRVPPPAPAPSTEGLPRAFLQSLRTLFDILDDRRRGCVHLREIESRWQGTDARELPRGVLEGLRQVAPASGYLTFERFVAGLRTSLLSADGGPRDP
TRAPARPGDQPPPPPQRLVFAPADEPRTVLERKPLPLGVRAPLAGPSAAARSPEQLCAPAEAAPCPAEPERSQSAALEPSSSADAGAVACRALEADSGDARRAPR
ARGERRRHTIASGVDCGLLKQMKELEQEKEVLLQGLEMMARGRDWYQQQLQRVQERQRRLGQSRASADFGAAGSPRPLGRLLPKVQEVARCLGELLAAACASRAL
PPSSSGPPCPALTSTSPPVWQQQTILMLKEQNRLLTQEVTEKSERITQLEQEKSALIKQLFEARALSQQDGGPLDSTFI
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MAGAAMAERGRVPPPAPAPSTEGLPRAFLQSLRTLFDILDDRRRGCVHLREIESRWQGTDARELPRGVLEGLRQVAPASGYLTFERFVAGLRTSLLSADGGPRDP
TRAPARPGDQPPPPPQRLVFAPADEPRTVLERKPLPLGVRAPLAGPSAAARSPEQLCAPAEAAPCPAEPERSQSAALEPSSSADAGAVACRALEADSGDARRAPR
ARGERRRHTIASGVDCGLLKQMKELEQEKEVLLQGLEMMARGRDWYQQQLQRVQERQRRLGQSRASADFGAAGSPRPLGRLLPKVQEVARCLGELLAAACASRAL
PPSSSGPPCPALTSTSPPVWQQQTILMLKEQNRLLTQEVTEKSERITQLEQEKSALIKQLFEARALSQQDGGPLDSTFI
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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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