PHYH Chromosome 10

Phytanoyl-CoA 2-hydroxylase
83 variants 83 Health Risk

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

What This Gene Does
This gene is a member of the PhyH family and encodes a peroxisomal protein that is involved in the alpha-oxidation of 3-methyl branched fatty acids. Specifically, this protein converts phytanoyl-CoA to 2-hydroxyphytanoyl-CoA. Mutations in this gene have been associated with Refsum disease (RD) and deficient protein activity has been associated with Zellweger syndrome and rhizomelic chondrodysplasia punctata. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Associated Conditions (30)
Phytanic acid storage disease
Nonsyndromic cleft lip palate
Inborn genetic diseases
Retinal dystrophy
Retinitis pigmentosa
PHYH-related disorder
Phytanoyl-CoA hydroxylase deficiency
Colon adenocarcinoma
Thymoma
Sarcoma
Acute myeloid leukemia
Malignant tumor of esophagus
Nonpapillary renal cell carcinoma
Familial cancer of breast
Intellectual disability
Optic atrophy
Vitamin D-dependent rickets type II with alopecia
Gastric cancer
Melanoma
Adrenocortical carcinoma
+10 more conditions
Key Variants
RS115198308
Conflicting classifications of pathogenicity
Phytanic acid storage disease, Phytanic acid storage disease
Health Risk
RS143734330
Conflicting classifications of pathogenicity
Phytanic acid storage disease, Phytanic acid storage disease
Health Risk
RS143957922
Conflicting classifications of pathogenicity
Phytanic acid storage disease, Phytanic acid storage disease
Health Risk
RS145404396
Conflicting classifications of pathogenicity
Nonsyndromic cleft lip palate, Phytanic acid storage disease, Nonsyndromic cleft lip palate
Health Risk
RS146190978
Conflicting classifications of pathogenicity
Health Risk
RS148951882
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1835617888
Conflicting classifications of pathogenicity
Retinal dystrophy, Retinal dystrophy
Health Risk
RS201499815
Conflicting classifications of pathogenicity
Retinitis pigmentosa, Phytanic acid storage disease, Retinal dystrophy
Health Risk
RS201936962
Conflicting classifications of pathogenicity
Phytanic acid storage disease, Inborn genetic diseases, Intellectual disability
Health Risk
RS201979258
Conflicting classifications of pathogenicity
Phytanic acid storage disease, Inborn genetic diseases, Retinal dystrophy
Health Risk
RS34571629
Conflicting classifications of pathogenicity
Phytanic acid storage disease, PHYH-related disorder, Retinal dystrophy
Health Risk
RS368542152
Conflicting classifications of pathogenicity
Phytanic acid storage disease, PHYH-related disorder, Phytanic acid storage disease
Health Risk
All Variants (83)
RSID Category Clinical Significance Conditions
RS115198308 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Phytanic acid storage disease
RS143734330 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Phytanic acid storage disease
RS143957922 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Phytanic acid storage disease
RS145404396 Health Risk Conflicting classifications of pathogenicity Nonsyndromic cleft lip palate, Phytanic acid storage disease, Nonsyndromic cleft lip palate
RS146190978 Health Risk Conflicting classifications of pathogenicity
RS148951882 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1835617888 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS201499815 Health Risk Conflicting classifications of pathogenicity Retinitis pigmentosa, Phytanic acid storage disease, Retinal dystrophy
RS201936962 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Inborn genetic diseases, Intellectual disability
RS201979258 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Inborn genetic diseases, Retinal dystrophy
RS34571629 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, PHYH-related disorder, Retinal dystrophy
RS368542152 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, PHYH-related disorder, Phytanic acid storage disease
RS372047384 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, PHYH-related disorder, Phytanic acid storage disease
RS375508574 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual disability, Inborn genetic diseases
RS566116760 Health Risk Conflicting classifications of pathogenicity Nonsyndromic cleft lip palate, Optic atrophy, Nonsyndromic cleft lip palate
RS62619919 Health Risk Conflicting classifications of pathogenicity Phytanic acid storage disease, Nonsyndromic cleft lip palate, Vitamin D-dependent rickets type II with alopecia
RS750819521 Health Risk Conflicting classifications of pathogenicity
RS770262329 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Phytanic acid storage disease, Retinal dystrophy
RS104894173 Health Risk Likely pathogenic REFSUM DISEASE, ADULT, 1
RS1448778830 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS1554784939 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS1835618953 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS1835721943 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS1835789883 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2131630730 Health Risk Likely pathogenic
RS2131640861 Health Risk Likely pathogenic
RS2131661125 Health Risk Likely pathogenic
RS2538635253 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538635262 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538635317 Health Risk Likely pathogenic
RS2538635322 Health Risk Likely pathogenic
RS2538643445 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538643520 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538650629 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538655957 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538656489 Health Risk Likely pathogenic
RS2538658717 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538664377 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS2538670229 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS747271385 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS751766259 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS752028596 Health Risk Likely pathogenic
RS753115080 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS759970314 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS761927136 Health Risk Likely pathogenic Phytanic acid storage disease, Hepatocellular carcinoma, Phytanic acid storage disease
RS769744387 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS770682604 Health Risk Likely pathogenic
RS774386869 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS797045100 Health Risk Likely pathogenic Phytanic acid storage disease, Phytanic acid storage disease
RS970229634 Health Risk Likely pathogenic PHYH-related disorder, PHYH-related disorder
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