Evidence Details for GPS1
Basic Information Top
Gene Symbol: | GPS1 ( COPS1,CSN1,MGC71287 ) |
---|---|
Gene Full Name: | G protein pathway suppressor 1 |
Band: | 17q25.3 |
Quick Links | Entrez ID:2873; OMIM: 601934; Uniprot ID:CSN1_HUMAN; ENSEMBL ID: ENSG00000169727; HGNC ID: 4549 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>GPS1|2873|nucleotide
ATGCCGCTGCCGGTTCAGGTGTTTAACTTGCAGGGGGCCGTGGAGCCCATGCAGATCGACGTGGACCCCCAGGAAGACCCGCAGAATGCACCTGACGTCAACTAC
GTGGTGGAGAACCCCAGCCTGGATCTGGAACAGTACGCGGCCAGCTACAGCGGCCTGATGCGCATCGAACGGCTGCAGTTCATTGCTGATCACTGCCCCACGCTG
CGGGTGGAGGCCCTGAAGATGGCCCTCTCCTTCGTGCAGAGAACCTTTAACGTGGACATGTACGAGGAGATCCACCGCAAGCTCTCAGAGGCCACCAGGTCCTCT
CTCAGGGAGCTGCAGAACGCACCCGACGCCATCCCTGAGAGCGGCGTGGAGCCCCCAGCCCTGGACACGGCCTGGGTGGAGGCCACGCGGAAGAAGGCGCTGCTG
AAGCTGGAGAAGCTGGACACAGACCTGAAGAACTACAAGGGCAACTCCATCAAAGAGAGCATCCGGCGCGGCCACGACGACCTGGGCGACCACTACCTGGACTGT
GGGGACCTCAGCAACGCCCTCAAGTGCTATTCCCGGGCCCGGGACTACTGCACCAGCGCCAAACACGTCATCAACATGTGCCTCAATGTCATCAAGGTCAGCGTC
TACTTGCAGAATTGGTCTCATGTGCTCAGCTACGTCAGCAAGGCTGAGTCCACCCCAGAGATTGCCGAGCAGCGAGGAGAGCGTGACAGCCAGACCCAGGCCATC
CTCACCAAGCTCAAGTGTGCCGCAGGCTTGGCAGAGCTGGCCGCCAGGAAGTACAAGCAGGCTGCCAAGTGCCTCCTGCTGGCTTCCTTTGATCACTGTGACTTC
CCTGAGCTGCTGTCCCCCAGCAACGTGGCCATCTACGGTGGCCTGTGCGCCTTGGCTACCTTTGACCGGCAGGAGCTGCAGCGCAATGTCATCTCCAGCAGCTCC
TTCAAGTTGTTCTTGGAGCTGGAGCCACAGGTCCGAGACATCATCTTCAAATTCTACGAGTCCAAGTACGCCTCATGTCTCAAGATGCTGGACGAGATGAAGGAC
AACCTGCTCCTGGACATGTATCTGGCCCCCCATGTCAGGACCCTGTACACCCAGATTCGCAACCGTGCCCTCATCCAGTATTTCAGCCCCTACGTGTCAGCCGAC
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ATGCCGCTGCCGGTTCAGGTGTTTAACTTGCAGGGGGCCGTGGAGCCCATGCAGATCGACGTGGACCCCCAGGAAGACCCGCAGAATGCACCTGACGTCAACTAC
GTGGTGGAGAACCCCAGCCTGGATCTGGAACAGTACGCGGCCAGCTACAGCGGCCTGATGCGCATCGAACGGCTGCAGTTCATTGCTGATCACTGCCCCACGCTG
CGGGTGGAGGCCCTGAAGATGGCCCTCTCCTTCGTGCAGAGAACCTTTAACGTGGACATGTACGAGGAGATCCACCGCAAGCTCTCAGAGGCCACCAGGTCCTCT
CTCAGGGAGCTGCAGAACGCACCCGACGCCATCCCTGAGAGCGGCGTGGAGCCCCCAGCCCTGGACACGGCCTGGGTGGAGGCCACGCGGAAGAAGGCGCTGCTG
AAGCTGGAGAAGCTGGACACAGACCTGAAGAACTACAAGGGCAACTCCATCAAAGAGAGCATCCGGCGCGGCCACGACGACCTGGGCGACCACTACCTGGACTGT
GGGGACCTCAGCAACGCCCTCAAGTGCTATTCCCGGGCCCGGGACTACTGCACCAGCGCCAAACACGTCATCAACATGTGCCTCAATGTCATCAAGGTCAGCGTC
TACTTGCAGAATTGGTCTCATGTGCTCAGCTACGTCAGCAAGGCTGAGTCCACCCCAGAGATTGCCGAGCAGCGAGGAGAGCGTGACAGCCAGACCCAGGCCATC
CTCACCAAGCTCAAGTGTGCCGCAGGCTTGGCAGAGCTGGCCGCCAGGAAGTACAAGCAGGCTGCCAAGTGCCTCCTGCTGGCTTCCTTTGATCACTGTGACTTC
CCTGAGCTGCTGTCCCCCAGCAACGTGGCCATCTACGGTGGCCTGTGCGCCTTGGCTACCTTTGACCGGCAGGAGCTGCAGCGCAATGTCATCTCCAGCAGCTCC
TTCAAGTTGTTCTTGGAGCTGGAGCCACAGGTCCGAGACATCATCTTCAAATTCTACGAGTCCAAGTACGCCTCATGTCTCAAGATGCTGGACGAGATGAAGGAC
AACCTGCTCCTGGACATGTATCTGGCCCCCCATGTCAGGACCCTGTACACCCAGATTCGCAACCGTGCCCTCATCCAGTATTTCAGCCCCTACGTGTCAGCCGAC
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>GPS1|2873|protein
MPLPVQVFNLQGAVEPMQIDVDPQEDPQNAPDVNYVVENPSLDLEQYAASYSGLMRIERLQFIADHCPTLRVEALKMALSFVQRTFNVDMYEEIHRKLSEATRSS
LRELQNAPDAIPESGVEPPALDTAWVEATRKKALLKLEKLDTDLKNYKGNSIKESIRRGHDDLGDHYLDCGDLSNALKCYSRARDYCTSAKHVINMCLNVIKVSV
YLQNWSHVLSYVSKAESTPEIAEQRGERDSQTQAILTKLKCAAGLAELAARKYKQAAKCLLLASFDHCDFPELLSPSNVAIYGGLCALATFDRQELQRNVISSSS
FKLFLELEPQVRDIIFKFYESKYASCLKMLDEMKDNLLLDMYLAPHVRTLYTQIRNRALIQYFSPYVSADMHRMAAAFNTTVAALEDELTQLILEGLISARVDSH
SKILYARDVDQRSTTFEKSLLMGKEFQRRAKAMMLRAAVLRNQIHVKSPPREGSQGELTPANSQSRMSTNM
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MPLPVQVFNLQGAVEPMQIDVDPQEDPQNAPDVNYVVENPSLDLEQYAASYSGLMRIERLQFIADHCPTLRVEALKMALSFVQRTFNVDMYEEIHRKLSEATRSS
LRELQNAPDAIPESGVEPPALDTAWVEATRKKALLKLEKLDTDLKNYKGNSIKESIRRGHDDLGDHYLDCGDLSNALKCYSRARDYCTSAKHVINMCLNVIKVSV
YLQNWSHVLSYVSKAESTPEIAEQRGERDSQTQAILTKLKCAAGLAELAARKYKQAAKCLLLASFDHCDFPELLSPSNVAIYGGLCALATFDRQELQRNVISSSS
FKLFLELEPQVRDIIFKFYESKYASCLKMLDEMKDNLLLDMYLAPHVRTLYTQIRNRALIQYFSPYVSADMHRMAAAFNTTVAALEDELTQLILEGLISARVDSH
SKILYARDVDQRSTTFEKSLLMGKEFQRRAKAMMLRAAVLRNQIHVKSPPREGSQGELTPANSQSRMSTNM
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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 (1) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 1 (1) | 0 (0) | 20 (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 | ||||||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 | ||
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 | ||||||
Auranen, 2002 | Finland | microsatellite-based genomic screen | autism | 19 | - | 19 | - | 54 | - | - |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
O'Roak BJ, 2012 | 1703 | 209 | 242 | Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
Turner TN, 2017 | - | Illumina X Ten | - | - | - | 476 | 476 | - | 2064 | Sanger sequencing |
Low Scale Gene Studies Top
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