Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family
- PMID: 2575483
- DOI: 10.1159/000132834
Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family
Abstract
In a large pedigree with autosomal dominant aniridia, we found close linkage between the aniridia locus AN2 and the markers catalase (CAT) (zeta = 7.27 at theta = 0.00) and D11S151 (zeta = 3.86 at theta = 0.10) flanking the AN2 locus on 11p13. Positive lod scores were also obtained for the 11p13----11p14 markers D11S16 and FSHB with the linkage group CAT/AN2/D11S151. We conclude that the autosomal dominant aniridia in this family is due to a mutation at the AN2 locus on 11p13. We have excluded linkage (zeta less than -2 at theta less than 0.18) between the aniridia and the chromosome 2p25 marker D2S1 (linked to ACP1).
Similar articles
-
Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13.Genomics. 1992 Aug;13(4):925-30. doi: 10.1016/0888-7543(92)90002-a. Genomics. 1992. PMID: 1505982
-
DNA diagnosis in a family with autosomal dominant aniridia.Ophthalmic Paediatr Genet. 1991 Dec;12(4):165-70. doi: 10.3109/13816819109025812. Ophthalmic Paediatr Genet. 1991. PMID: 1815167
-
Long-range restriction map around 11p13 aniridia locus.Somat Cell Mol Genet. 1989 Nov;15(6):605-15. doi: 10.1007/BF01534921. Somat Cell Mol Genet. 1989. PMID: 2556802
-
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.Am J Hum Genet. 1980 May;32(3):314-31. Am J Hum Genet. 1980. PMID: 6247908 Free PMC article. Review.
-
Gene mapping and other tools for discovery.Epilepsia. 1990;31 Suppl 3:S11-8. doi: 10.1111/j.1528-1157.1990.tb05854.x. Epilepsia. 1990. PMID: 1977582 Review.
Cited by
-
A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family.Mol Vis. 2012;18:465-70. Epub 2012 Feb 16. Mol Vis. 2012. PMID: 22393272 Free PMC article.
-
Mutation of the PAX6 gene in patients with autosomal dominant keratitis.Am J Hum Genet. 1995 Sep;57(3):539-48. Am J Hum Genet. 1995. PMID: 7668281 Free PMC article.
-
Mutation analysis of paired box 6 gene in inherited aniridia in northern China.Mol Vis. 2013 May 30;19:1169-77. Print 2013. Mol Vis. 2013. PMID: 23734086 Free PMC article.
-
The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities-A review.Clin Exp Ophthalmol. 2022 Mar;50(2):143-162. doi: 10.1111/ceo.14035. Epub 2022 Jan 17. Clin Exp Ophthalmol. 2022. PMID: 35037362 Free PMC article. Review.
-
Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.Hum Genet. 1994 Oct;94(4):331-8. doi: 10.1007/BF00201588. Hum Genet. 1994. PMID: 7927324
Publication types
MeSH terms
Substances
LinkOut - more resources
Miscellaneous