Curated Information
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Home > Curated Information Page > PubMed Id: 15900227
Lachman HM, Stopkova P, Rafael MA, Saito T (2005) Association of schizophrenia in African Americans to polymorphism in synapsin III gene. Psychiatr Genet 15, 127-32 15900227
This page summarizes selected information from the record referenced above and curated into PhosphoSitePlus®, a comprehensive online resource for the study of protein post-translational modifications (NAR, 2015, 43:D512-20). To learn more about the scope of PhosphoSitePlus®, click here.
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S470-p - SYN3 (human)
Modsite: PQGQQPLsPQsGsPQ SwissProt Entrez-Gene
Orthologous residues
SYN3 (human): S470‑p, SYN3 (mouse): S469‑p, SYN3 (rat): S469‑p
Characterization
Methods used to characterize site in vivo mutation of modification site
Disease tissue studied:  schizophrenia
Relevant cell lines - cell types - tissues:  blood, brain
Cellular systems studied:  primary cells, tissue
Species studied:  human
Comments:  genotyping done through blood sample
Associated Diseases
Diseases Alterations Comments
schizophrenia mutation of site