Evidence Details for C15orf2
Basic Information Top
Gene Symbol: | C15orf2 ( - ) |
---|---|
Gene Full Name: | chromosome 15 open reading frame 2 |
Band: | 15q11-q13 |
Quick Links | Entrez ID:23742; OMIM: 610922; Uniprot ID:CO002_HUMAN; ENSEMBL ID: ENSG00000185823; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C15orf2|23742|nucleotide
ATGGGCAATTTACTTAGTAAATTTAGACCCGGGTGCCGCCGCCGGCCCCTGCCAGGGCCAGGGCGTGGCGCCCCCGCTCCCCTGTCCCGGGACGCCTCCCCGCCC
GGTCGGGCTCACTCTGTACCCACCCCGCGCCCTTTCCGCGGCCTGTTCCGCCGGAACGCCCGTCGCAGGCCTTCAGCAGCCAGCATCTTCGTCGCCCCTAAGAGG
CCGTGTCCTCTCCCTCGGGCTGCGGCCGCCCCTCTGGGGGTCCTGCCGGCTGTGGGTTGGGGGCTGGCCATCAGGAAGACACCCATGCTGCCTGCTCGGAACCCC
CCGAGGTTTGGACACCCCAGTTCCGTAAGGATCCCTCCTCCCAGCCGCATGTTCACTCTCCTGCTGCCTTCACCACGTGAGCCGGCGGTCAAGGCCAGGAAGCCC
ATCCCAGCCACTCTCCTGGAGGAGACCGAGGTGTGGGCCCAAGAAGGGCCCAGAAGAGTGAAGAAGGATGAGGATCCGGTGCAGATCGAAGGGGAGGATGACGAG
AAAAGGACCCCCCTTAGCAGCGGAGAAGCATCGTCCACATCCAGGTCCCAGGGCACCCAGGGAGACGTGGCCTCCTTCAGATGCAGCCCTGGGCCTCTGGAGGGA
AATGTCTACCACAAGTTCTCAGAAAACAGCATGAGTGAGAAGGCCCAGGCGTCTCCAGCGAGCTCCTGCTTGGAAGGCCCTGCCATGCCCAGCACACACAGCCAG
GCCGGATGTGCCCGGCATCTTGGAAAGCCTGATCCGGATGCAACAGCGCCCCCTGAGCCAGCCGTTGGCTGCTCCCTGCTGCAGCAGAAGTTGGCTGCGGAAGTG
CTGAATGAAGAGCCACCGCCCAGCTCCCTAGGCTTGCCGATTCCGCTGATGTCCGGAAAGAGGATGCCTGATGAGAAGCCTTTCTGTATTCCTCCAAGGAGCGCT
GCTCCTCCCAGAGCTGCCCGCAACAGGCCCTGCAAAAGGAAAATGTCGATTCCATTGCTGCTGCCGCTGCCCCCTTCACTGCCATTGCTGTGGGATCGAGGTGAG
CTTCCCCCACCTGCTAAGCTCCCCTGCCTGTCTGTTGAGGGAGACCTACACACCTTGGAGAAGAGCCCTGAGTATAAAAGGAATAGCAGAATCTTGGAGGATAAA
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ATGGGCAATTTACTTAGTAAATTTAGACCCGGGTGCCGCCGCCGGCCCCTGCCAGGGCCAGGGCGTGGCGCCCCCGCTCCCCTGTCCCGGGACGCCTCCCCGCCC
GGTCGGGCTCACTCTGTACCCACCCCGCGCCCTTTCCGCGGCCTGTTCCGCCGGAACGCCCGTCGCAGGCCTTCAGCAGCCAGCATCTTCGTCGCCCCTAAGAGG
CCGTGTCCTCTCCCTCGGGCTGCGGCCGCCCCTCTGGGGGTCCTGCCGGCTGTGGGTTGGGGGCTGGCCATCAGGAAGACACCCATGCTGCCTGCTCGGAACCCC
CCGAGGTTTGGACACCCCAGTTCCGTAAGGATCCCTCCTCCCAGCCGCATGTTCACTCTCCTGCTGCCTTCACCACGTGAGCCGGCGGTCAAGGCCAGGAAGCCC
ATCCCAGCCACTCTCCTGGAGGAGACCGAGGTGTGGGCCCAAGAAGGGCCCAGAAGAGTGAAGAAGGATGAGGATCCGGTGCAGATCGAAGGGGAGGATGACGAG
AAAAGGACCCCCCTTAGCAGCGGAGAAGCATCGTCCACATCCAGGTCCCAGGGCACCCAGGGAGACGTGGCCTCCTTCAGATGCAGCCCTGGGCCTCTGGAGGGA
AATGTCTACCACAAGTTCTCAGAAAACAGCATGAGTGAGAAGGCCCAGGCGTCTCCAGCGAGCTCCTGCTTGGAAGGCCCTGCCATGCCCAGCACACACAGCCAG
GCCGGATGTGCCCGGCATCTTGGAAAGCCTGATCCGGATGCAACAGCGCCCCCTGAGCCAGCCGTTGGCTGCTCCCTGCTGCAGCAGAAGTTGGCTGCGGAAGTG
CTGAATGAAGAGCCACCGCCCAGCTCCCTAGGCTTGCCGATTCCGCTGATGTCCGGAAAGAGGATGCCTGATGAGAAGCCTTTCTGTATTCCTCCAAGGAGCGCT
GCTCCTCCCAGAGCTGCCCGCAACAGGCCCTGCAAAAGGAAAATGTCGATTCCATTGCTGCTGCCGCTGCCCCCTTCACTGCCATTGCTGTGGGATCGAGGTGAG
CTTCCCCCACCTGCTAAGCTCCCCTGCCTGTCTGTTGAGGGAGACCTACACACCTTGGAGAAGAGCCCTGAGTATAAAAGGAATAGCAGAATCTTGGAGGATAAA
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>C15orf2|23742|protein
MGNLLSKFRPGCRRRPLPGPGRGAPAPLSRDASPPGRAHSVPTPRPFRGLFRRNARRRPSAASIFVAPKRPCPLPRAAAAPLGVLPAVGWGLAIRKTPMLPARNP
PRFGHPSSVRIPPPSRMFTLLLPSPREPAVKARKPIPATLLEETEVWAQEGPRRVKKDEDPVQIEGEDDEKRTPLSSGEASSTSRSQGTQGDVASFRCSPGPLEG
NVYHKFSENSMSEKAQASPASSCLEGPAMPSTHSQAGCARHLGKPDPDATAPPEPAVGCSLLQQKLAAEVLNEEPPPSSLGLPIPLMSGKRMPDEKPFCIPPRSA
APPRAARNRPCKRKMSIPLLLPLPPSLPLLWDRGELPPPAKLPCLSVEGDLHTLEKSPEYKRNSRILEDKTETMTNSSITQPAPSFSQPVQTTDSLPLTTYTSQV
SAPLPIPDLADLATGPLILPIPPLSTTPKMDEKIAFTIPNSPLALPADLVPILGDQSNEKGGSYNSVVGAAPLTSDPPTPPSSTPSFKPPVTRESPISMCVDSPP
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MGNLLSKFRPGCRRRPLPGPGRGAPAPLSRDASPPGRAHSVPTPRPFRGLFRRNARRRPSAASIFVAPKRPCPLPRAAAAPLGVLPAVGWGLAIRKTPMLPARNP
PRFGHPSSVRIPPPSRMFTLLLPSPREPAVKARKPIPATLLEETEVWAQEGPRRVKKDEDPVQIEGEDDEKRTPLSSGEASSTSRSQGTQGDVASFRCSPGPLEG
NVYHKFSENSMSEKAQASPASSCLEGPAMPSTHSQAGCARHLGKPDPDATAPPEPAVGCSLLQQKLAAEVLNEEPPPSSLGLPIPLMSGKRMPDEKPFCIPPRSA
APPRAARNRPCKRKMSIPLLLPLPPSLPLLWDRGELPPPAKLPCLSVEGDLHTLEKSPEYKRNSRILEDKTETMTNSSITQPAPSFSQPVQTTDSLPLTTYTSQV
SAPLPIPDLADLATGPLILPIPPLSTTPKMDEKIAFTIPNSPLALPADLVPILGDQSNEKGGSYNSVVGAAPLTSDPPTPPSSTPSFKPPVTRESPISMCVDSPP
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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) | 2 (17) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 4 (17) |
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 | ||||||
Wolpert, 2000 | - | STS mapping | autism | 3 | - | 3 | - | 3 | - | 3 | ||
Wassink, 2001 | USA | Chromosomal analysis of G-band | autism | - | - | - | - | 278 | - | 278 | ||
Silva, 2002 | - | FISH | autism | - | - | - | - | 1 | - | 1 | ||
Keller, 2003 | USA | FISH | ASD | - | - | - | - | 2 | - | 2 | ||
Sahoo, 2005 | USA | aCGH | autism | - | - | - | - | 9 | - | 9 | ||
Wassink, 2007 | USA | FISH | PDD | - | - | - | - | 104 | - | 104 | ||
Sebat, 2007 | USA | aCGH | autism | 165 | 118 | 47 | 99 | 195 | 196 | 391 | ||
Szatmari, 2007 | Europe, North America | SNP microarray | ASD | 1491 | - | - | - | - | - | 0 | ||
Weiss, 2008 | USA, Ireland | aCGH, SNP microarray | ASD | 751 | - | - | - | 2252 | 23502 | 25754 | ||
Marshall, 2008 | - | SNP microarray | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 | ||
Christian, 2008 | USA | aCGH | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 | ||
Bucan, 2009 | USA | SNP microarray | autism, ASD | 912 | - | 912 | - | - | 1488 | 1488 | ||
Gregory, 2009 | USA | aCGH | ASD | - | - | - | - | 119 | 54 | 173 | ||
Bremer, 2009 | - | aCGH | ASD | - | - | - | - | 148 | - | 148 | ||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 | ||
Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top
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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