NHERF1 Chromosome 17
NHERF family PDZ scaffold protein 1
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What This Gene Does
This gene encodes a sodium/hydrogen exchanger regulatory cofactor. The protein interacts with and regulates various proteins including the cystic fibrosis transmembrane conductance regulator and G-protein coupled receptors such as the beta2-adrenergic receptor and the parathyroid hormone 1 receptor. The protein also interacts with proteins that function as linkers between integral membrane and cytoskeletal proteins. The protein localizes to actin-rich structures including membrane ruffles, microvilli, and filopodia. Mutations in this gene result in hypophosphatemic nephrolithiasis/osteoporosis type 2, and loss of heterozygosity of this gene is implicated in breast cancer.[provided by RefSeq, Sep 2009]
Gene Info
Gene Group
"PDZ domain containing|MicroRNA protein coding host genes|NHERF family PDZ scaffold proteins"
Locus Type
gene with protein product
Location
17q25.1
Ensembl
ENSG00000109062
Associated Conditions (8)
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Clear cell carcinoma of kidney
Malignant tumor of urinary bladder
Familial cancer of breast
NHERF1-related disorder
Hypophosphatemic nephrolithiasis/osteoporosis 2
Inborn genetic diseases
Chronic kidney disease
Key Variants
RS138547261
Conflicting classifications of pathogenicity
Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Clear cell carcinoma of kidney, Malignant tumor of urinary bladder
Health Risk
RS139622189
Conflicting classifications of pathogenicity
Health Risk
RS141613848
Conflicting classifications of pathogenicity
NHERF1-related disorder, Hypophosphatemic nephrolithiasis/osteoporosis 2, NHERF1-related disorder
Health Risk
RS149161808
Conflicting classifications of pathogenicity
NHERF1-related disorder, Inborn genetic diseases, NHERF1-related disorder
Health Risk
RS35738271
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS41282065
Conflicting classifications of pathogenicity
Hypophosphatemic nephrolithiasis/osteoporosis 2, Chronic kidney disease, NHERF1-related disorder
Health Risk
RS752725349
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS764753729
Conflicting classifications of pathogenicity
Health Risk
RS765897805
Conflicting classifications of pathogenicity
Hypophosphatemic nephrolithiasis/osteoporosis 2, Inborn genetic diseases, NHERF1-related disorder
Health Risk
All Variants (9)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS138547261 | Health Risk | Conflicting classifications of pathogenicity | Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Clear cell carcinoma of kidney, Malignant tumor of urinary bladder |
| RS139622189 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS141613848 | Health Risk | Conflicting classifications of pathogenicity | NHERF1-related disorder, Hypophosphatemic nephrolithiasis/osteoporosis 2, NHERF1-related disorder |
| RS149161808 | Health Risk | Conflicting classifications of pathogenicity | NHERF1-related disorder, Inborn genetic diseases, NHERF1-related disorder |
| RS35738271 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS41282065 | Health Risk | Conflicting classifications of pathogenicity | Hypophosphatemic nephrolithiasis/osteoporosis 2, Chronic kidney disease, NHERF1-related disorder |
| RS752725349 | Health Risk | Conflicting classifications of pathogenicity | Inborn genetic diseases, Inborn genetic diseases |
| RS764753729 | Health Risk | Conflicting classifications of pathogenicity | — |
| RS765897805 | Health Risk | Conflicting classifications of pathogenicity | Hypophosphatemic nephrolithiasis/osteoporosis 2, Inborn genetic diseases, NHERF1-related disorder |