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AIC Aicardi syndrome [ Homo sapiens (human) ]

Gene ID: 192, updated on 2-Oct-2019

Summary

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Gene symbol
AIC
Gene description
Aicardi syndrome
Primary source
MIM:304050
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:
Xp22

Bibliography

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Related articles in PubMed

  1. Agenesis of corpus callosum, ocular, and skeletal anomalies (X-linked dominant Aicardi's syndrome) in a girl with balanced X/3 translocation. Ropers HH, et al. Hum Genet, 1982. PMID 6818132
  2. Heterogeneity of clinical severity and molecular lesions in Aicardi syndrome. Neidich JA, et al. J Pediatr, 1990 Jun. PMID 1971852

GeneRIFs: Gene References Into Functions

Phenotypes

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Aicardi syndrome

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases