Detailed description page of humcfs

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NPHS1 details
Primary information
gene_nameNPHS1
Humcfs IdHumcfs_4424
chromosome_numberchromosome19
nameFRA19A
chrlocation32400001-59128983
cytoband19q13
type5-azacytidine
frequencyCommon
gene_ensembl_idENSG00000161270
havana_transcript_idOTTHUMT00000452554
gene_location35826380-35851838
gene_orientation-
exon_idENSE00002753500, ENSE00001153484, ENSE00001057256, ENSE00001384533, ENSE00001479239, ENSE00001505335, ENSE00001368371, ENSE00001385699, ENSE00001373160, ENSE00001364309, ENSE00001725083, ENSE000017477
exon_number28
gene_descriptionnephrosis 1, congenital, Finnish type (nephrin)
disease_descriptionIGA Glomerulonephritis,Hypoalbuminemia,Autosomal dominant focal segmental glomerulosclerosis,Pre-Eclampsia,Alport Syndrome,Athetosis,Hematuria,Glomerulonephritis,Glomerulosclerosis (disorder),Interstitial fibrosis,Segmental glomerulosclerosis,Hyperparathyroidism, Secondary,Finnish congenital nephrotic syndrome,Nephroblastoma,Focal glomerulosclerosis,Nephrotic Syndrome, Minimal Change,Diabetes Mellitus, Insulin-Dependent,Diabetic Nephropathy,Glomerulonephritis, Minimal Change,Lipoid nephrosis,Ichthyosis linearis circumflexa,AIDS-Associated Nephropathy,Diabetes Mellitus, Non-Insulin-Dependent,Kidney Failure,Malignant tumor of colon,Proteinuria Adverse Event,Kidney Diseases,Diverticulosis,Chronic kidney disease stage 5,Nephrotic Syndrome,Nephrotic syndrome in children,Malonic aciduria,Nephrosis,Cyst,Nephrosis, congenital,Kidney Failure, Chronic,Hypertensive disease,Albuminuria,Membranous glomerulonephritis,Hyperhomocysteinemia,Proteinuria,Colon Carcinoma,Steroid-resistant nephrotic syndro
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID2579891
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