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
RS190769116 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis, Finnish congenital nephrotic syndrome
RS191850409 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
RS1973070541 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973103431 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS1973129633 Health Risk Conflicting classifications of pathogenicity Focal segmental glomerulosclerosis, Focal segmental glomerulosclerosis
RS199646884 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS199735886 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS199888357 Health Risk Conflicting classifications of pathogenicity Kidney disorder, NPHS1-related disorder, Kidney disorder
RS199932050 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200253809 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS200265333 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS200621047 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200905486 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS201263480 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, NPHS1-related disorder
RS201503587 Health Risk Conflicting classifications of pathogenicity Familial idiopathic steroid-resistant nephrotic syndrome, Congenital nephrotic syndrome, NPHS1-related disorder
RS201738778 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS201822740 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513765932 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513774296 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS2513784716 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS28939695 Health Risk Conflicting classifications of pathogenicity Proteinuria, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
RS34673364 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS34761059 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
RS34982899 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS35238405 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis, Finnish congenital nephrotic syndrome
RS35240811 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
RS367976914 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome, Focal segmental glomerulosclerosis
RS368523939 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS368639377 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Congenital nephrotic syndrome
RS368913905 Health Risk Conflicting classifications of pathogenicity Proteinuria, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
RS369787477 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Inborn genetic diseases, Finnish congenital nephrotic syndrome
RS370046047 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
RS370387270 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome, Focal segmental glomerulosclerosis
RS370645778 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Congenital nephrotic syndrome
RS370844834 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Finnish congenital nephrotic syndrome, Inborn genetic diseases
RS371646734 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Congenital nephrotic syndrome
RS371907999 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Congenital nephrotic syndrome
RS372069596 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Congenital nephrotic syndrome
RS372079888 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS373264146 Health Risk Conflicting classifications of pathogenicity Microscopic hematuria, Finnish congenital nephrotic syndrome, NPHS1-related disorder
RS373835033 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS373931233 Health Risk Conflicting classifications of pathogenicity
RS375587420 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Congenital nephrotic syndrome
RS375670819 Health Risk Conflicting classifications of pathogenicity Congenital nephrotic syndrome, Finnish congenital nephrotic syndrome, Focal segmental glomerulosclerosis
RS375861433 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, NPHS1-related disorder, Finnish congenital nephrotic syndrome
RS377446423 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS386833861 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, NPHS1-related disorder, Unexplained young onset end-stage renal disease
RS386833862 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS386833879 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
RS386833933 Health Risk Conflicting classifications of pathogenicity Finnish congenital nephrotic syndrome, Finnish congenital nephrotic syndrome
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