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Relevance to Autism

Two de novo missense variants that were predicted to be probably damaging (defined as MPC 2) were identified in the AP2S1 gene in ASD probands from the Simons Simplex Collection and the Autism Sequencing Consortium (Iossifov et al., 2014; Satterstrom et al., 2020), while two additional protein-truncating variants in this gene were observed in case samples from the Danish iPSYCH study (Satterstrom et al., 2020). TADA analysis of de novo variants from the Simons Simplex Collection and the Autism Sequencing Consortium and protein-truncating variants from iPSYCH in Satterstrom et al., 2020 identified AP2S1 as a candidate gene with a false discovery rate (FDR) 0.01.

Molecular Function

One of two major clathrin-associated adaptor complexes, AP-2, is a heterotetramer which is associated with the plasma membrane. This complex is composed of two large chains, a medium chain, and a small chain. This gene encodes the small chain of this complex.

External Links

        

References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
The contribution of de novo coding mutations to autism spectrum disorder
ASD
Support
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Stereotypy
Support
The adaptor protein 2 (AP2) complex modulates habituation and behavioral selection across multiple pathways and time windows
Support
Integrating de novo and inherited variants in 42
ASD
Recent recommendation
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
ASD

Rare

Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
 GEN1148R001 
 missense_variant 
 c.191G>A 
 p.Gly64Asp 
 De novo 
  
 Simplex 
 GEN1148R002 
 missense_variant 
 c.76C>T 
 p.Arg26Trp 
 De novo 
  
 Simplex 
 GEN1148R003 
 missense_variant 
 c.29G>A 
 p.Cys10Tyr 
 De novo 
  
  
 GEN1148R004 
 missense_variant 
 c.187_188delinsAA 
 p.Ala63Asn 
 De novo 
  
 Simplex 

Common

No Common Variants Available
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
19
Deletion-Duplication
 14
 
19
Duplication
 2
 

No Animal Model Data Available

 

No Interactions Available
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