Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7533
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Type: Journal article
Title: Localisation of a 10q breakpoint within the PAX2 gene in a patient with a de novo t(10;13) translocation and optic nerve coloboma-renal disease
Author: Narahara, K.
Baker, E.
Ito, S.
Yokoyama, Y.
Yu, S.
Hewitt, D.
Sutherland, G.
Eccles, M.
Richards, R.
Citation: Journal of Medical Genetics, 1997; 34(3):213-216
Publisher: BMJ PUBLISHING GROUP
Issue Date: 1997
ISSN: 0022-2593
1468-6244
Statement of
Responsibility: 
Koji Narahara, Elizabeth Baker, Shigeru Ito, Yuji Yokoyama, Sui Yu, Duncan Hewitt, Grant R Sutherland, Michael R Eccles, Robert I Richards
Abstract: We describe a 5 year old boy with a de novo t(10;13) translocation and optic nerve coloboma-renal disease (ONCR). On the basis of GTG banding analysis of prometaphase chromosomes, the patient's karyotype was interpreted as either 46,XY,t(10;13)(q24.3;q12.3) or t(10;13) (q25.2;q14.1). Fluorescence in situ hybridisation (FISH) studies using a YAC clone containing the PAX2 gene and YAC clones adjoining FRA10B at 10q25.2 showed that the 10q breakpoint had occurred just within the PAX2 gene and was proximal to FRA10B. These FISH results suggest that the translocation causes a disruption of the PAX2 gene and leads to ONCR, in agreement with the recent reports of PAX2 mutations in two unrelated families with ONCR. Furthermore, we refined the regional mapping of the human PAX2 gene to the junction of bands 10q24.3 and 10q25.1.
Keywords: Optic nerve coloboma-renal disease; PAX2; t(10; 13) translocation
Rights: Copyright status unknown
RMID: 0030005513
DOI: 10.1136/jmg.34.3.213
Appears in Collections:Paediatrics publications

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