PHOX2A Chromosome 11

Paired like homeobox 2A
2 variants 2 Health Risk

Upload your DNA to see your personal genotypes for variants in PHOX2A.

What This Gene Does
The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system. It regulates the expression of tyrosine hydroxylase and dopamine beta-hydroxylase, two catecholaminergic biosynthetic enzymes essential for the differentiation and maintenance of the noradrenergic neurotransmitter phenotype. The encoded protein has also been shown to regulate transcription of the alpha3 nicotinic acetylcholine receptor gene. Mutations in this gene have been associated with autosomal recessive congenital fibrosis of the extraocular muscles. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
PRD class homeoboxes and pseudogenes
Locus Type
gene with protein product
Location
11q13.4
Ensembl
ENSG00000165462
Associated Conditions (3)
Fibrosis of extraocular muscles
congenital
2
Key Variants
All Variants (2)
RSID Category Clinical Significance Conditions
RS1178102382 Health Risk Pathogenic Fibrosis of extraocular muscles, congenital, 2
RS1590729541 Health Risk Pathogenic Fibrosis of extraocular muscles, congenital, 2
Sign Up to Analyze Your DNA Log In