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NYS2 nystagmus 2, congenital autosomal dominant [ Homo sapiens (human) ]

Gene ID: 4933, updated on 2-Oct-2019

Summary

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Gene symbol
NYS2
Gene description
nystagmus 2, congenital autosomal dominant
Primary source
MIM:164100
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NYSA

Genomic context

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Location:
6p12

Bibliography

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Related articles in PubMed

  1. Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12. Kerrison JB, et al. Am J Ophthalmol, 1998 Jan. PMID 9437315
  2. A gene for autosomal dominant congenital nystagmus localizes to 6p12. Kerrison JB, et al. Genomics, 1996 May 1. PMID 8661013
  3. Hereditary congenital nystagmus and gaze-holding failure: the role of the neural integrator. Dell'Osso LF, et al. Neurology, 1993 Sep. PMID 8414024
  4. Congenital nystagmus cosegregating with a balanced 7;15 translocation. Patton MA, et al. J Med Genet, 1993 Jun. PMID 8326501, Free PMC Article
  5. Infantile nystagmus: a prospective study of spasmus nutans, and congenital nystagmus, and unclassified nystagmus of infancy. Jayalakshmi P, et al. J Pediatr, 1970 Aug. PMID 5504065

GeneRIFs: Gene References Into Functions

Phenotypes

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nystagmus 2, congenital autosomal dominant

General gene information

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Markers

Property

  • phenotype only

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