Gene: PTCHD1
Alternate names for this Gene: AUTSX4
Gene Summary: This gene encodes a membrane protein with a patched domain. The encoded protein is similar to Drosophila proteins which act as receptors for the morphogen sonic hedgehog. Deletions in this gene, which is located on the X chromosome, are associated with intellectual disability and autism (PMID: 21091464, PMID: 20844286).
Gene is located in Chromosome: X
Location in Chromosome : Xp22.11
Description of this Gene: patched domain containing 1
Type of Gene: protein-coding
rs5925760 in
PTCHD1 gene and
Cytokine Measurement
PMID 22610502 2012 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.
rs1555912049 in
PTCHD1 gene and
Movement Disorders
PMID 25782667 2015 Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.
PMID 25131214 2015 Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
PMID 20844286 2010 Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
PMID 23871722 2013 XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
PMID 21091464 2011 Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.
rs1555912049 in
PTCHD1 gene and
Muscle hypotonia
PMID 23871722 2013 XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing.
PMID 25131214 2015 Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder.
PMID 21091464 2011 Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism.
PMID 20844286 2010 Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.
PMID 25782667 2015 Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.