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Relevance to Autism

This gene was originally identified as an ASD candidate gene based on its enrichment in an autism-associated protein interaction module. Sequencing of post-mortem brain tissue from 25 ASD cases resulted in the identification of significant non-synonymous variants in this gene with an expected false-positive rate at 0.1, confirming the involvement of this module with autism; this finding was further validated by exome sequencing of an independent cohort of 505 ASD cases and 491 controls (Li et al., 2014).

Molecular Function

Inward rectifying potassium channel that is activated by phosphatidylinositol 4,5-bisphosphate and that probably participates in controlling the resting membrane potential in electrically excitable cells. Probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues.

External Links

        

References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Integrated systems analysis reveals a molecular network underlying autism spectrum disorders.
ASD
Support
Integrating de novo and inherited variants in 42
ASD

Rare

Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
 GEN686R001 
 missense_variant 
 c.433G>A 
 p.Gly145Ser 
 Unknown 
  
 Unknown 
 GEN686R002 
 missense_variant 
 c.1206C>T 
 p.Asp402= 
 Unknown 
  
 Unknown 
 GEN686R003 
 synonymous_variant 
 c.45G>A 
 p.Ser15%3D 
 De novo 
  
  
 GEN686R004 
 synonymous_variant 
 c.687C>T 
 p.Arg229%3D 
 De novo 
  
 Multiplex 

Common

No Common Variants Available
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
17
Deletion-Duplication
 63
  construct
17
Deletion-Duplication
 4
 
17
Duplication
 7
 
17
Duplication
 1
 
17
Duplication
 1
 
17
Duplication
 2
 
17
Duplication
 1
 
17
Duplication
 1
 

No Animal Model Data Available

No PIN Data Available
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