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. 2022 Sep 13;14:939793. doi: 10.3389/fnsyn.2022.939793

TABLE 1.

Scaffold proteins that have been reported to be associated with neurological or psychiatric disorders from human genetics studies.

Genes Reported disorders and references
SHANK1 Autism (Sato et al., 2012)
SHANK2 Autism, ID (intellectual disability) (Berkel et al., 2010; Satterstrom et al., 2020)
SHANK3 Autism (Durand et al., 2007; Moessner et al., 2007; Satterstrom et al., 2020)
SYNGAP1 ID (Intellectual disability) (Hamdan et al., 2009; Rauch et al., 2012; Deciphering Developmental Disorders Study., 2015, 2017), autism (Hamdan et al., 2011; Satterstrom et al., 2020)
GRIP1 Autism (Mejias et al., 2011)
HOMER1 Autism (Kelleher<suffix>III</suffix>, Geigenmuller et al., 2012), schizophrenia (Norton et al., 2003), depression (Rao et al., 2016)
PSD95 Schizophrenia, ID, autism (Coley and Gao, 2018)
CASK ID (Hayashi et al., 2008; Najm et al., 2008), brain malformation (Najm et al., 2008)
PICCOLO Major depressive disorder (Sullivan et al., 2009), bipolar disorder (Choi et al., 2011; Chen et al., 2021), schizophrenia (Chen et al., 2021)
BASSOON Bipolar disorder, schizophrenia (Chen et al., 2021)
STXBP1/MUNC18-1 Dravet Syndrome (Carvill et al., 2014), Infantile epileptic encephalopathy (Saitsu et al., 2008)