P4HB Chromosome 17

Prolyl 4-hydroxylase subunit beta
11 variants 11 Health Risk

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What This Gene Does
This gene encodes the beta subunit of prolyl 4-hydroxylase, a highly abundant multifunctional enzyme that belongs to the protein disulfide isomerase family. When present as a tetramer consisting of two alpha and two beta subunits, this enzyme is involved in hydroxylation of prolyl residues in preprocollagen. This enzyme is also a disulfide isomerase containing two thioredoxin domains that catalyze the formation, breakage and rearrangement of disulfide bonds. Other known functions include its ability to act as a chaperone that inhibits aggregation of misfolded proteins in a concentration-dependent manner, its ability to bind thyroid hormone, its role in both the influx and efflux of S-nitrosothiol-bound nitric oxide, and its function as a subunit of the microsomal triglyceride transfer protein complex. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Protein disulfide isomerases
Locus Type
gene with protein product
Location
17q25.3
Ensembl
ENSG00000185624
Associated Conditions (3)
Inborn genetic diseases
P4HB-related disorder
Cole-Carpenter syndrome 1
Key Variants
All Variants (11)
RSID Category Clinical Significance Conditions
RS143758998 Health Risk Conflicting classifications of pathogenicity
RS145040305 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS146810022 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS146846893 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201906397 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS376060719 Health Risk Conflicting classifications of pathogenicity P4HB-related disorder, Inborn genetic diseases, P4HB-related disorder
RS756303311 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS761976262 Health Risk Conflicting classifications of pathogenicity Cole-Carpenter syndrome 1, Inborn genetic diseases, Cole-Carpenter syndrome 1
RS2143371167 Health Risk Likely pathogenic Cole-Carpenter syndrome 1, Cole-Carpenter syndrome 1
RS2509949884 Health Risk Likely pathogenic
RS786204843 Health Risk Pathogenic Cole-Carpenter syndrome 1, Cole-Carpenter syndrome 1
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