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Relevance to Autism

Integration of familial whole-exome datasets of 3,531 individuals from 1,704 simplex ASD families and 50 multiplex ASD families and expression data from the BrainSpan Atlas of the Developmental Human Brain in Luo et al., 2020 identified a neurodevelopmentally co-regulated, sex-differentially expressed cluster of exons enriched with ASD-segregating deleterious variants in the TMEM134 gene (Bonferroni-corrected cluster P-value of 1.17E-02).

Molecular Function

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References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
A multidimensional precision medicine approach identifies an autism subtype characterized by dyslipidemia
ASD
Support
Mutational Landscape of Autism Spectrum Disorder Brain Tissue
ASD

Rare

Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
 GEN1217R001 
 stop_gained 
 c.250C>T 
 p.Arg84Ter 
 Familial 
  
  
 GEN1217R002 
 missense_variant 
 c.531C>G 
 p.Cys177Trp 
 De novo 
  
  
 GEN1217R003 
 frameshift_variant 
 c.485del 
 p.Phe162SerfsTer11 
 Familial 
 Paternal 
 Multiplex 

Common

No Common Variants Available
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
11
Deletion-Duplication
 1
 
11
Deletion
 1
 

No Animal Model Data Available

No PIN Data Available
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