PAH Chromosome 12

Phenylalanine hydroxylase
675 variants 675 Health Risk

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What This Gene Does
This gene encodes a member of the biopterin-dependent aromatic amino acid hydroxylase protein family. The encoded phenylalanine hydroxylase enzyme hydroxylates phenylalanine to tyrosine and is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria. [provided by RefSeq, Aug 2017]
Gene Info
Gene Group
Aromatic amino acid hydroxylase family
Locus Type
gene with protein product
Location
12q23.2
Ensembl
ENSG00000171759
Associated Conditions (25)
Phenylketonuria
Inborn genetic diseases
Hyperphenylalaninemia
See cases
PAH-related disorder
RASopathy
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency
Hepatocellular carcinoma
Pituitary hormone deficiency
combined
2
Clear cell carcinoma of kidney
Malignant tumor of esophagus
Polymicrogyria
perisylvian
with cerebellar hypoplasia and arthrogryposis
Mild non-PKU hyperphenylalanemia
Malignant tumor of breast
Propionic acidemia
Pulmonary hypertension
+5 more conditions
Key Variants
All Variants (675)
RSID Category Clinical Significance Conditions
RS62642094 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642095 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, PAH-related disorder
RS62642906 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS62642907 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642908 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642910 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642915 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS62642920 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642921 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642926 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Inborn genetic diseases
RS62642928 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642932 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642933 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Phenylketonuria
RS62642934 Health Risk Pathogenic Hyperphenylalaninemia, Phenylketonuria, Hyperphenylalaninemia
RS62642935 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Phenylketonuria
RS62642936 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642937 Health Risk Pathogenic Hyperphenylalaninemia, Phenylketonuria, Marfanoid habitus and intellectual disability
RS62642940 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62642941 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62644465 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62644467 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62644477 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS62644499 Health Risk Pathogenic Hyperphenylalaninemia, Phenylketonuria, PAH-related disorder
RS62644501 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62651568 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS62895363 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS63102461 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS63581460 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS63749676 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS63749677 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS672601294 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS74486803 Health Risk Pathogenic Hyperphenylalaninemia, Phenylketonuria, 6-Pyruvoyl-tetrahydrobiopterin synthase deficiency
RS74503222 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS748337823 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS751203209 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS75166491 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS75193786 Health Risk Pathogenic Phenylketonuria, See cases, Inborn genetic diseases
RS752255985 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS760830761 Health Risk Pathogenic Phenylketonuria, Phenylketonuria, Phenylketonuria
RS76212747 Health Risk Pathogenic Hyperphenylalaninemia, Phenylketonuria, Inborn genetic diseases
RS762949770 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS76296470 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS76394784 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Phenylketonuria
RS76542238 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Phenylketonuria
RS765552494 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS766107583 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS778154939 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS78655458 Health Risk Pathogenic Phenylketonuria, PAH-related disorder, Phenylketonuria
RS79635844 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
RS886042078 Health Risk Pathogenic Phenylketonuria, Phenylketonuria
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