NHERF1 Chromosome 17

NHERF family PDZ scaffold protein 1
9 variants 9 Health Risk

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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
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
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