Evidence Details for GPC5
 Basic Information Top
| Gene Symbol: | GPC5 ( - ) | 
|---|---|
| Gene Full Name: | glypican 5 | 
| Band: | 13q31.3 | 
| Quick Links | Entrez ID:2262; OMIM: 602446; Uniprot ID:GPC5_HUMAN; ENSEMBL ID: ENSG00000179399; HGNC ID: 4453 | 
| Relate to Another Database: | SFARIGene; denovo-db | 
 Sequences Top
>GPC5|2262|nucleotide
ATGGACGCACAGACCTGGCCCGTGGGCTTTCGCTGCCTCCTCCTTCTGGCCCTGGTTGGGTCCGCCCGCAGCGAGGGCGTGCAGACCTGCGAAGAAGTTCGGAAA
CTTTTCCAGTGGCGGCTGCTGGGAGCTGTCAGGGGGCTGCCGGATTCGCCGCGGGCAGGACCTGATCTTCAGGTTTGCATATCCAAAAAGCCTACATGTTGCACC
AGGAAGATGGAGGAGAGATATCAGATTGCGGCTCGCCAGGATATGCAGCAGTTTCTTCAAACGTCCAGCTCTACATTAAAGTTTCTAATATCTCGAAATGCGGCT
GCTTTTCAAGAAACCCTTGAAACTCTCATCAAACAAGCAGAAAATTACACCAGTATACTTTTTTGCAGTACCTACAGGAACATGGCCTTGGAGGCTGCTGCTTCG
GTTCAGGAGTTCTTCACTGATGTGGGGCTGTATTTATTTGGTGCGGATGTTAATCCTGAAGAATTTGTAAACAGATTTTTTGACAGTCTTTTTCCTCTGGTCTAC
AACCACCTCATTAACCCTGGTGTGACTGACAGTTCCCTGGAATACTCAGAATGCATCCGGATGGCTCGCCGGGATGTGAGTCCATTTGGTAATATTCCCCAAAGA
GTAATGGGACAGATGGGGAGGTCCCTGCTGCCCAGCCGCACTTTTCTGCAGGCACTCAATCTGGGCATTGAAGTCATCAACACCACAGACTATCTGCACTTCTCC
AAAGAGTGCAGCAGAGCCCTCCTGAAGATGCAATACTGCCCGCACTGCCAAGGCCTGGCGCTCACTAAGCCTTGTATGGGATACTGCCTCAATGTCATGCGAGGC
TGCCTGGCGCACATGGCGGAGCTTAATCCACACTGGCATGCATATATCCGGTCGTTGGAAGAACTCTCGGATGCAATGCATGGAACATACGACATTGGACACGTG
CTGCTGAACTTTCACTTGCTTGTTAATGATGCTGTGTTACAGGCTCACCTCAATGGACAAAAATTATTGGAACAGGTAAATAGGATTTGTGGCCGCCCTGTAAGA
ACACCCACACAAAGCCCCCGTTGTTCTTTTGATCAGAGCAAAGAGAAGCATGGAATGAAGACCACCACAAGGAACAGTGAAGAGACGCTTGCCAACAGAAGAAAA
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ATGGACGCACAGACCTGGCCCGTGGGCTTTCGCTGCCTCCTCCTTCTGGCCCTGGTTGGGTCCGCCCGCAGCGAGGGCGTGCAGACCTGCGAAGAAGTTCGGAAA
CTTTTCCAGTGGCGGCTGCTGGGAGCTGTCAGGGGGCTGCCGGATTCGCCGCGGGCAGGACCTGATCTTCAGGTTTGCATATCCAAAAAGCCTACATGTTGCACC
AGGAAGATGGAGGAGAGATATCAGATTGCGGCTCGCCAGGATATGCAGCAGTTTCTTCAAACGTCCAGCTCTACATTAAAGTTTCTAATATCTCGAAATGCGGCT
GCTTTTCAAGAAACCCTTGAAACTCTCATCAAACAAGCAGAAAATTACACCAGTATACTTTTTTGCAGTACCTACAGGAACATGGCCTTGGAGGCTGCTGCTTCG
GTTCAGGAGTTCTTCACTGATGTGGGGCTGTATTTATTTGGTGCGGATGTTAATCCTGAAGAATTTGTAAACAGATTTTTTGACAGTCTTTTTCCTCTGGTCTAC
AACCACCTCATTAACCCTGGTGTGACTGACAGTTCCCTGGAATACTCAGAATGCATCCGGATGGCTCGCCGGGATGTGAGTCCATTTGGTAATATTCCCCAAAGA
GTAATGGGACAGATGGGGAGGTCCCTGCTGCCCAGCCGCACTTTTCTGCAGGCACTCAATCTGGGCATTGAAGTCATCAACACCACAGACTATCTGCACTTCTCC
AAAGAGTGCAGCAGAGCCCTCCTGAAGATGCAATACTGCCCGCACTGCCAAGGCCTGGCGCTCACTAAGCCTTGTATGGGATACTGCCTCAATGTCATGCGAGGC
TGCCTGGCGCACATGGCGGAGCTTAATCCACACTGGCATGCATATATCCGGTCGTTGGAAGAACTCTCGGATGCAATGCATGGAACATACGACATTGGACACGTG
CTGCTGAACTTTCACTTGCTTGTTAATGATGCTGTGTTACAGGCTCACCTCAATGGACAAAAATTATTGGAACAGGTAAATAGGATTTGTGGCCGCCCTGTAAGA
ACACCCACACAAAGCCCCCGTTGTTCTTTTGATCAGAGCAAAGAGAAGCATGGAATGAAGACCACCACAAGGAACAGTGAAGAGACGCTTGCCAACAGAAGAAAA
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>GPC5|2262|protein
MDAQTWPVGFRCLLLLALVGSARSEGVQTCEEVRKLFQWRLLGAVRGLPDSPRAGPDLQVCISKKPTCCTRKMEERYQIAARQDMQQFLQTSSSTLKFLISRNAA
AFQETLETLIKQAENYTSILFCSTYRNMALEAAASVQEFFTDVGLYLFGADVNPEEFVNRFFDSLFPLVYNHLINPGVTDSSLEYSECIRMARRDVSPFGNIPQR
VMGQMGRSLLPSRTFLQALNLGIEVINTTDYLHFSKECSRALLKMQYCPHCQGLALTKPCMGYCLNVMRGCLAHMAELNPHWHAYIRSLEELSDAMHGTYDIGHV
LLNFHLLVNDAVLQAHLNGQKLLEQVNRICGRPVRTPTQSPRCSFDQSKEKHGMKTTTRNSEETLANRRKEFINSLRLYRSFYGGLADQLCANELAAADGLPCWN
GEDIVKSYTQRVVGNGIKAQSGNPEVKVKGIDPVINQIIDKLKHVVQLLQGRSPKPDKWELLQLGSGGGMVEQVSGDCDDEDGCGGSGSGEVKRTLKITDWMPDD
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MDAQTWPVGFRCLLLLALVGSARSEGVQTCEEVRKLFQWRLLGAVRGLPDSPRAGPDLQVCISKKPTCCTRKMEERYQIAARQDMQQFLQTSSSTLKFLISRNAA
AFQETLETLIKQAENYTSILFCSTYRNMALEAAASVQEFFTDVGLYLFGADVNPEEFVNRFFDSLFPLVYNHLINPGVTDSSLEYSECIRMARRDVSPFGNIPQR
VMGQMGRSLLPSRTFLQALNLGIEVINTTDYLHFSKECSRALLKMQYCPHCQGLALTKPCMGYCLNVMRGCLAHMAELNPHWHAYIRSLEELSDAMHGTYDIGHV
LLNFHLLVNDAVLQAHLNGQKLLEQVNRICGRPVRTPTQSPRCSFDQSKEKHGMKTTTRNSEETLANRRKEFINSLRLYRSFYGGLADQLCANELAAADGLPCWN
GEDIVKSYTQRVVGNGIKAQSGNPEVKVKGIDPVINQIIDKLKHVVQLLQGRSPKPDKWELLQLGSGGGMVEQVSGDCDDEDGCGGSGSGEVKRTLKITDWMPDD
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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 (1) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (2) | 2 (2) | 0 (1) | 0 (0) | 4 (8) | 
Syndromic Autism Gene Top
Genome-Wide Association Studies (By Ethnic Group) Top
 Family Based Association Studies: 1
| Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women)  | 
			ADI-R | ADOS | Diagnosis | Age (range)  | 
			IQ (range)  | 
		||||||
| CAUCASIAN | |||||||||||
| Hussman, 2011_1 | Discovery | Illumina Infinium Human 1 M beadship | 597 | - (-)  | ![]()  | ![]()  | ASD | - -  | 
				- -  | ||
 Case Control Based Association Studies: 0
| Reference | Stage | Platform | ASD Cases | Normal Controls | Result | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women)  | 
			ADI-R | ADOS | Diagnosis | Age (range)  | 
			IQ | #Subjects (% Women)  | 
			Age (range)  | 
		|||||
| No Evidence. | ||||||||||||
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 | 
| Hemmat M, 2014 | - | - | - | - | ASD | - | - | - | - | 1 | - | 1 | 
Linkage Studies Top
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 | 
|---|---|---|---|---|
| De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism | 
| Fromer M, 2014 | - | - | 94 | De novo mutations in schizophrenia implicate synaptic networks. | 
NGS Mosaic SNV Studies Top
| Reference | Case Number | Family Number | Mosaic Number | Title | 
|---|---|---|---|---|
| Lim ET, 2017 | - | 5947 | 376 | Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder | 
| Freed D, 2016 | - | 2388 | 5 | The Contribution of Mosaic Variants to Autism Spectrum Disorder. | 
NGS Other Studies Top
| Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | ||||||||
| Doan RN, 2016 | - | - | - | - | ASD | - | - | - | - | - | 
 Low Scale Gene Studies Top
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