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NYS3 nystagmus 3, congenital autosomal dominant [ Homo sapiens (human) ]

Gene ID: 4934, updated on 2-Oct-2019

Summary

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Gene symbol
NYS3
Gene description
nystagmus 3, congenital autosomal dominant
Primary source
MIM:608345
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CN

Genomic context

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Location:
7p11

Bibliography

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Related articles in PubMed

  1. Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus. Klein C, et al. Genomics, 1998 Nov 15. PMID 9806847

GeneRIFs: Gene References Into Functions

Phenotypes

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nystagmus 3, congenital autosomal dominant

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases