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Relevance to Autism

Five SNPs within PCDHA7 (rs251379, rs1119032, rs17119271, rs155806, and rs17119346) showed significant association with autism in a family-based association study using 14 SNPs within the PCDHA gene cluster in 841 ASD families (574 of which were multiplex) obtained from the Autism Genetic Resource Exchange (AGRE) (Anitha et al., 2012).

Molecular Function

This gene is a member of the protocadherin alpha gene cluster, one of three related gene clusters tandemly linked on chromosome five that demonstrate an unusual genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 cadherin superfamily genes related to the mouse CNR genes and consists of 13 highly similar and 2 more distantly related coding sequences. The tandem array of 15 N-terminal exons, or variable exons, are followed by downstream C-terminal exons, or constant exons, which are shared by all genes in the cluster. The large, uninterrupted N-terminal exons each encode six cadherin ectodomains while the C-terminal exons encode the cytoplasmic domain. These neural cadherin-like cell adhesion proteins are integral plasma membrane proteins that most likely play a critical role in the establishment and function of specific cell-cell connections in the brain.

External Links

        

References

Type
Title
Type of Disorder
Associated Disorders
Author, Year
Primary
Protocadherin (PCDHA) as a novel susceptibility gene for autism.
ASD
Support
Phenotype-to-genotype approach reveals head-circumference-associated genes in an autism spectrum disorder cohort.
ASD
Macrocephaly
Support
Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks.
ASD
Support
De novo gene disruptions in children on the autistic spectrum.
ASD
Support
Integrating de novo and inherited variants in 42
ASD
Support
Mutational Landscape of Autism Spectrum Disorder Brain Tissue
ASD
Recent Recommendation
Identification of CTCF as a master regulator of the clustered protocadherin genes.

Rare

Variant ID
Variant Type
Allele Change
Residue Change
Inheritance Pattern
Inheritance Association
Family Type
Author, Year
 GEN447R001 
 intron_variant 
 c.2355+47565del 
  
 De novo 
  
 Simplex 
 GEN447R002 
 stop_gained 
 c.21C>A 
 p.Tyr7Ter 
 Familial 
 Maternal 
 Multiplex 
 GEN447R003 
 stop_gained 
 c.21C>A 
 p.Tyr7Ter 
 Familial 
 Paternal 
 Simplex 
 GEN447R004 
 synonymous_variant 
 c.45G>T 
 p.Leu15%3D 
 Unknown 
  
  
 GEN447R005 
 missense_variant 
 c.1206G>C 
 p.Lys402Asn 
 De novo 
  
  

Common

Variant ID
Polymorphism
SNP ID
Allele Change
Residue Change
Population Origin
Population Stage
Author, Year
 GEN447C001 
 intron_variant 
 rs251379 
 c.2355+42599G>A 
 T/C 
 AGRE: 1467 patients from 841 total families (574 of which were multiplex) 
 Discovery 
 GEN447C002 
 intron_variant 
 rs1119032 
 c.2355+66108A>G 
  
 AGRE: 1467 patients from 841 total families (574 of which were multiplex) 
 Discovery 
 GEN447C003 
 intron_variant 
 rs17119271 
 c.2356-48828T>C 
  
 AGRE: 1467 patients from 841 total families (574 of which were multiplex) 
 Discovery 
 GEN447C004 
 intron_variant 
 rs155806 
 c.2356-8694A>G 
 T/C 
 AGRE: 1467 patients from 841 total families (574 of which were multiplex) 
 Discovery 
 GEN447C005 
 intron_variant 
 rs17119346 
 c.2503+11686G>A 
  
 AGRE: 1467 patients from 841 total families (574 of which were multiplex) 
 Discovery 
Chromosome
CNV Locus
CNV Type
# of studies
Animal Model
5
Duplication
 1
 
5
Deletion
 1
 
5
Duplication
 1
 
5
Duplication
 3
 
5
Deletion
 1
 
5
Deletion-Duplication
 9
 

No Animal Model Data Available

No PIN Data Available
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