The NPHS1 gene homepage

General information
Gene symbol NPHS1
Gene name nephrosis 1, congenital, Finnish type (nephrin)
Chromosome 19
Chromosomal band q12-q13.1
Imprinted Unknown
Genomic reference NG_013356.2
Transcript reference NM_004646.3
Exon/intron information NM_004646.3 exon/intron table
Associated with diseases NPHS, NPHS1
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 395
Unique public DNA variants reported 236
Individuals with public variants 287
Hidden variants 13
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement nÂș 200754 - the GEN2PHEN project.

This database was initially part of the Finnish Disease Resource (FinDis; Polvi et al: Hum Mutat. 2013:34:1458-66). We gratefully acknowledge the support of Juha Muilu acting as curator until 2015.
Date created April 05, 2011
Date last updated April 09, 2024
Version NPHS1:240409

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_004646.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/NPHS1
External URL Finnish Disease Database (FinDis)
HGNC 7908
Entrez Gene 4868
PubMed articles NPHS1
OMIM - Gene 602716
OMIM - Diseases NPHS1 (nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF)))
HGMD NPHS1
GeneCards NPHS1
GeneTests NPHS1
Orphanet NPHS1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000050 19 nephrosis 1, congenital, Finnish type (nephrin) NM_004646.3 NP_004637.1 395


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