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GLC3C glaucoma 3, primary congenital, C [ Homo sapiens (human) ]

Gene ID: 399565, updated on 31-Aug-2024

Summary

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Official Symbol
GLC3Cprovided by HGNC
Official Full Name
glaucoma 3, primary congenital, Cprovided by HGNC
Primary source
MIM:613085
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
14q24.3-q31.1

Bibliography

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Related articles in PubMed

  1. Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma. Chen X, et al. Front Biosci (Landmark Ed), 2011 Jun 1. PMID 21622161
  2. Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies. Sivadorai P, et al. Clin Genet, 2008 Jul. PMID 18537981

GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. Significant transmission disequilibrium (P=0.0010) occurred between the haplotype TAACG of rs2111701- rs4020123- rs4903696- rs11159318- rs177216 in primary congenital glaucoma.
    Title: Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma.
  2. Observational study of gene-disease association. (HuGE Navigator)
    Title: Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.
Submit: New GeneRIF Correction

Phenotypes

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Associated conditions

Description Tests
glaucoma 3, primary congenital, C
OMIM: 613085GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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