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GLC3B glaucoma 3, primary infantile, B [ Homo sapiens (human) ]

Gene ID: 2728, updated on 2-Oct-2019

Summary

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Gene symbol
GLC3B
Gene description
glaucoma 3, primary infantile, B
Primary source
MIM:600975
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:
1p36

Bibliography

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Related articles in PubMed

  1. A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region. Akarsu AN, et al. Hum Mol Genet, 1996 Aug. PMID 8842741
  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. 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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glaucoma 3, primary infantile, B

General gene information

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Property

  • phenotype only

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