Human (GRCh37.p13)
Description

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

Gene Synonyms

CNF, NPHN, nephrin

Location

Chromosome 19: 36,316,866-36,360,189 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 5 transcripts (splice variants), 3 paralogues and is associated with 5 phenotypes.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000378910.5NPHS1-00142761241aa
 
Protein coding
CCDS32996O60500 NM_004646.3Ensembl CanonicalGENCODE Basic
ENST00000353632.6NPHS1-00237411201aa
 
Protein coding
O60500 -GENCODE Basic
ENST00000591817.1NPHS1-005581No protein
 
Processed transcript
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ENST00000585400.1NPHS1-003999No protein
 
Retained intron
---
ENST00000592132.1NPHS1-004561No protein
 
Retained intron
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