NPHS1 Chromosome 19

NPHS1 adhesion molecule, nephrin
533 variants 3 Drug Response 530 Health Risk

Upload your DNA to see your personal genotypes for variants in NPHS1.

What This Gene Does
This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]
Gene Info
Gene Group
"Fibronectin type III domain containing|V-set domain containing|C2-set domain containing"
Locus Type
gene with protein product
Location
19q13.12
Ensembl
ENSG00000161270
Associated Conditions (19)
Corticosteroids response
Finnish congenital nephrotic syndrome
NPHS1-related disorder
Nephrotic syndrome
Congenital nephrotic syndrome
Focal segmental glomerulosclerosis
Inborn genetic diseases
Proteinuria
Familial idiopathic steroid-resistant nephrotic syndrome
Kidney disorder
Gastric cancer
Microscopic hematuria
Unexplained young onset end-stage renal disease
Atypical hemolytic-uremic syndrome
Congenital and infantile nephrotic syndrome
Steroid-resistant nephrotic syndrome
Nephrotic range proteinuria
Infantile Nephrotic syndrome
See cases
Key Variants
RS1972875644
drug response
Corticosteroids response, Corticosteroids response
Drug Response
RS1972884983
drug response
Corticosteroids response, Corticosteroids response
Drug Response
RS1973075631
drug response
Corticosteroids response, Corticosteroids response
Drug Response
RS1000712587
Conflicting classifications of pathogenicity
Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
Health Risk
RS1131691606
Conflicting classifications of pathogenicity
Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
Health Risk
RS114112112
Conflicting classifications of pathogenicity
Finnish congenital nephrotic syndrome, NPHS1-related disorder, Finnish congenital nephrotic syndrome
Health Risk
RS114203578
Conflicting classifications of pathogenicity
Finnish congenital nephrotic syndrome, Nephrotic syndrome, Finnish congenital nephrotic syndrome
Health Risk
RS114385015
Conflicting classifications of pathogenicity
Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
Health Risk
RS114428177
Conflicting classifications of pathogenicity
Inborn genetic diseases, Finnish congenital nephrotic syndrome, Inborn genetic diseases
Health Risk
RS114595892
Conflicting classifications of pathogenicity
Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
Health Risk
RS114615449
Conflicting classifications of pathogenicity
Proteinuria, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
Health Risk
RS114728208
Conflicting classifications of pathogenicity
Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
Health Risk
All Variants (533)
RSID Category Clinical Significance Conditions
RS150038620 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS150855173 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1555762591 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1555763460 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1568456335 Health Risk Pathogenic
RS1599845689 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1972879158 Health Risk Pathogenic
RS1972948538 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973023933 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973089176 Health Risk Pathogenic
RS1973123878 Health Risk Pathogenic
RS1973124127 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973169054 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973180778 Health Risk Pathogenic
RS1973192570 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2146807976 Health Risk Pathogenic
RS2146812210 Health Risk Pathogenic
RS2146816347 Health Risk Pathogenic
RS2146819931 Health Risk Pathogenic
RS2146821009 Health Risk Pathogenic
RS2146822012 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2146823207 Health Risk Pathogenic
RS2146823441 Health Risk Pathogenic
RS2146823645 Health Risk Pathogenic
RS2146826513 Health Risk Pathogenic
RS2146827068 Health Risk Pathogenic
RS2146827686 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2146828473 Health Risk Pathogenic
RS2146831183 Health Risk Pathogenic
RS2146831931 Health Risk Pathogenic
RS2146832020 Health Risk Pathogenic
RS2513754818 Health Risk Pathogenic
RS2513761918 Health Risk Pathogenic
RS2513765812 Health Risk Pathogenic
RS2513766222 Health Risk Pathogenic
RS2513766238 Health Risk Pathogenic
RS2513768304 Health Risk Pathogenic
RS2513768306 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513769058 Health Risk Pathogenic
RS2513769085 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513769124 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513769198 Health Risk Pathogenic
RS2513769207 Health Risk Pathogenic
RS2513769477 Health Risk Pathogenic
RS2513769577 Health Risk Pathogenic
RS2513770468 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513771917 Health Risk Pathogenic Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513773107 Health Risk Pathogenic
RS2513773230 Health Risk Pathogenic
RS2513773327 Health Risk Pathogenic
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