TY - JOUR
T1 - Location of the gene involving the Small eye mutation on mouse chromosome 2 suggests homology with human aniridia 2 (AN2)
AU - van der Meer-de Jong, Riet
AU - Dickinson, Mary E.
AU - Woychik, Richard P.
AU - Stubbs, Lisa
AU - Hetherington, Colin
AU - Hogan, Brigid L.M.
N1 - Funding Information:
i Research jointly by the Medical Research Council of Great Britain and the National Institutes of Health (ROl EY080000-01) and by the Office of Health and Environmental Research, U.S. Department of Energy under Contract DE-AC05-840R21400 with Martin Marietta Energy Systems, Inc. The U.S. Government’s right to retain a nonexclusive royalty-free license in and to the copyright covering this paper, for governmental purposes, is acknowledged.
PY - 1990/6
Y1 - 1990/6
N2 - Using and interspecific backcross, we have mapped the gene involved in the mouse Small eye mutation (SeyMH) relative to six cloned markers on chromosome 2 (Hox-5.1, Cas-1, Fshb, Bmp-2a, and ld) and the agouti locus. The results suggest that the Sey gene maps between Fshb and Cas-1. Human mapping studies have shown that the aniridia (AN2) gene, which is part of the Wilms tumor susceptibility, aniridia, genitourinary abnormalities, and mental retardation (WARG) complex, is also between FSHB and CAT on human chromosome 11. The conserved linkage of the cloned markers and the similarity of the Sey/+ and AN2/+ phenotypes suggest that the gene involved in the Sey mutation is the mouse homolog of the human AN2 gene.
AB - Using and interspecific backcross, we have mapped the gene involved in the mouse Small eye mutation (SeyMH) relative to six cloned markers on chromosome 2 (Hox-5.1, Cas-1, Fshb, Bmp-2a, and ld) and the agouti locus. The results suggest that the Sey gene maps between Fshb and Cas-1. Human mapping studies have shown that the aniridia (AN2) gene, which is part of the Wilms tumor susceptibility, aniridia, genitourinary abnormalities, and mental retardation (WARG) complex, is also between FSHB and CAT on human chromosome 11. The conserved linkage of the cloned markers and the similarity of the Sey/+ and AN2/+ phenotypes suggest that the gene involved in the Sey mutation is the mouse homolog of the human AN2 gene.
UR - http://www.scopus.com/inward/record.url?scp=0025308738&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025308738&partnerID=8YFLogxK
U2 - 10.1016/0888-7543(90)90550-E
DO - 10.1016/0888-7543(90)90550-E
M3 - Article
C2 - 2347591
AN - SCOPUS:0025308738
SN - 0888-7543
VL - 7
SP - 270
EP - 275
JO - Genomics
JF - Genomics
IS - 2
ER -