AutismKB 2.0

Evidence Details for GPC5


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Basic Information Top
Gene Symbol:GPC5 ( - )
Gene Full Name: glypican 5
Band: 13q31.3
Quick LinksEntrez 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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>GPC5|2262|protein
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, qPCRASD - - - - 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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  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018