Description

nephrosis 1, congenital, Finnish type (nephrin) [Source:HGNC Symbol;Acc:HGNC:7908]

Synonyms

CNF, NPHN

Location

Chromosome 19: 35,825,964-35,869,287 reverse strand.

GRCh38:CM000681.2

About this gene

This gene has 5 transcripts (splice variants), 58 orthologues, 3 paralogues, is a member of 1 Ensembl protein family and is associated with 6 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NPHS1-001ENST0000037891042761241aaENSP00000368190
 
Protein coding
CCDS32996O60500 NM_004646
NP_004637
TSL:1GENCODE basicAPPRIS P1
NPHS1-002ENST0000035363237411201aaENSP00000343634
 
Protein coding
-O60500 -TSL:5GENCODE basic
NPHS1-005ENST00000591817581No protein-
 
Processed transcript
---TSL:5
NPHS1-003ENST00000585400999No protein-
 
Retained intron
---TSL:1
NPHS1-004ENST00000592132561No protein-
 
Retained intron
---TSL:3

Gene-based displays