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Relevance to Autism

JMY was identified as an ASD candidate gene in Wilfert et al., 2021 based on the discovery of private likely gene-disruptive (LGD) variants in this highly constrained (pLI 0.99) gene that were exclusively transmitted to four ASD probands in four independent families.

Molecular Function

Acts both as a nuclear p53/TP53-cofactor and a cytoplasmic regulator of actin dynamics depending on conditions. In nucleus, acts as a cofactor that increases p53/TP53 response via its interaction with p300/EP300. Increases p53/TP53-dependent transcription and apoptosis, suggesting an important role in p53/TP53 stress response such as DNA damage. In cytoplasm, acts as a nucleation-promoting factor for both branched and unbranched actin filaments. Activates the Arp2/3 complex to induce branched actin filament networks. Also catalyzes actin polymerization in the absence of Arp2/3, creating unbranched filaments. Contributes to cell motility by controlling actin dynamics. May promote the rapid formation of a branched actin network by first nucleating new mother filaments and then activating Arp2/3 to branch off these filaments. The p53/TP53-cofactor and actin activator activities are regulated via its subcellular location.

External Links

        

References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Recent ultra-rare inherited variants implicate new autism candidate risk genes
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
 GEN1274R001 
 stop_gained 
 c.454C>T 
 p.Gln152Ter 
 Familial 
  
 Simplex 
 GEN1274R002 
 stop_gained 
 c.1564C>T 
 p.Arg522Ter 
 Familial 
  
 Simplex 
 GEN1274R003 
 frameshift_variant 
 c.2456del 
 p.Pro819LeufsTer69 
 Familial 
  
 Simplex 
 GEN1274R004 
 stop_gained 
 c.1375C>T 
 p.Arg459Ter 
 Familial 
  
 Simplex 
 GEN1274R005 
 missense_variant 
 c.2615G>A 
 p.Arg872Gln 
 De novo 
  
 Simplex 

Common

No Common Variants Available
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
5
Duplication
 1
 
5
Duplication
 4
 
5
Duplication
 1
 
5
Deletion-Duplication
 18
 
5
Duplication
 1
 

No Animal Model Data Available

 

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