P4HB Chromosome 17
Prolyl 4-hydroxylase subunit beta
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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
RS143758998
Conflicting classifications of pathogenicity
Health Risk
RS145040305
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146810022
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS146846893
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS201906397
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS376060719
Conflicting classifications of pathogenicity
P4HB-related disorder, Inborn genetic diseases, P4HB-related disorder
Health Risk
RS756303311
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS761976262
Conflicting classifications of pathogenicity
Cole-Carpenter syndrome 1, Inborn genetic diseases, Cole-Carpenter syndrome 1
Health Risk
RS2143371167
Likely pathogenic
Cole-Carpenter syndrome 1, Cole-Carpenter syndrome 1
Health Risk
RS2509949884
Likely pathogenic
Health Risk
RS786204843
Pathogenic
Cole-Carpenter syndrome 1, Cole-Carpenter syndrome 1
Health Risk
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 |