PDE2A

On this page, you will find information about a genetic change that was identified in a UDN participant. We are trying to find others with the same or similar condition.

Sharing information on this website is not a requirement of UDN participation. Only descriptions about participants who give explicit consent will appear here.

A change in this gene was identified in a female, age 3, with global developmental delay, failure to thrive, absent speech, and low muscle tone (hypotonia) (read full description).

Date of Report

Jun 24, 2019

Full Name

phosphodiesterase 2A

Location

Chromosome 11 (11q13.4)

Function

The PDE2A gene plays an important role in the regulation of ATP production inside the mitochondria (Monterisi et al., 2017).

Database Links

GeneCards: PDE2A

NCBI Gene: 5138

OMIM: 602658

UniProtKB/Swiss-Prot: O00408

Clinical Significance

A change in this gene was identified in a UDN participant. Research is underway to see if this change is causing symptoms in this participant.

Gene PDE2A

Inheritance Pattern Unknown

Position (hg19) chr11:g.72296600A>C

Transcript NM_002599.4

DNA Change c.1220T>G

Protein Change p.Leu407Arg

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