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IGAN1 IgA nephropathy [ Homo sapiens (human) ]

Gene ID: 60498, updated on 16-Aug-2019

Summary

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Gene symbol
IGAN1
Gene description
IgA nephropathy
Primary source
MIM:161950
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
IGAN

Genomic context

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Location:
6q22-q23

Bibliography

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Related articles in PubMed

  1. Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy. Gharavi AG, et al. J Am Soc Nephrol, 2008 May. PMID 18272841, Free PMC Article
  2. Analysis of O-glycan heterogeneity in IgA1 myeloma proteins by Fourier transform ion cyclotron resonance mass spectrometry: implications for IgA nephropathy. Renfrow MB, et al. Anal Bioanal Chem, 2007 Nov. PMID 17712550
  3. Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels. Moldoveanu Z, et al. Kidney Int, 2007 Jun. PMID 17342176
  4. IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23. Gharavi AG, et al. Nat Genet, 2000 Nov. PMID 11062479

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. abnormal IgA1 glycosylation is an inherited rather than acquired trait
    Title: Aberrant IgA1 glycosylation is inherited in familial and sporadic IgA nephropathy.
  2. analysis of IgA1 O-glycan heterogeneity by use of FT-ICR MS and liquid chromatography
    Title: Analysis of O-glycan heterogeneity in IgA1 myeloma proteins by Fourier transform ion cyclotron resonance mass spectrometry: implications for IgA nephropathy.
  3. Patients with IGAN have increased serum galactose-deficient IgA1 levels.
    Title: Patients with IgA nephropathy have increased serum galactose-deficient IgA1 levels.
Submit: New GeneRIF Correction

Phenotypes

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IgA nephropathy

General gene information

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Property

  • phenotype only

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