The Nfe2l1 gene maps to distal mouse Chromosome 11

1996 ◽  
Vol 7 (1) ◽  
pp. 89-89 ◽  
Author(s):  
J. McKie ◽  
P. J. Scambler
Keyword(s):  
Mouse Chromosome ◽  
Chromosome 11 ◽  
Distal Mouse Chromosome ◽  
Distal Mouse ◽  
Mouse Chromosome 11 ◽  
Gene Maps

The clf1 gene maps to a 2- to 3-cM region of distal mouse Chromosome 11

1996 ◽  
Vol 7 (10) ◽  
pp. 789-789 ◽  
Author(s):  
D. M. Juriloff ◽  
M. J. Harris ◽  
D. G. Mah
Keyword(s):  
Mouse Chromosome ◽  
Chromosome 11 ◽  
Distal Mouse Chromosome ◽  
Distal Mouse ◽  
Mouse Chromosome 11 ◽  
Gene Maps

scholarly journals A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11

1996 ◽  
Vol 93 (26) ◽  
pp. 15352-15357 ◽  
Author(s):  
K. L. Mohlke ◽  
W. C. Nichols ◽  
R. J. Westrick ◽  
E. K. Novak ◽  
K. A. Cooney ◽  
...  
Keyword(s):  
Mouse Chromosome ◽  
Von Willebrand Factor ◽  
Modifier Gene ◽  
Chromosome 11 ◽  
Factor Level ◽  
Distal Mouse Chromosome ◽  
Distal Mouse ◽  
Von Willebrand ◽  
Mouse Chromosome 11 ◽  
Willebrand Factor

scholarly journals The polar-lethal Ovum mutant gene maps to the distal portion of mouse chromosome 11.

Genetics ◽  
1992 ◽  
Vol 132 (1) ◽  
pp. 241-246
Author(s):  
C Sapienza ◽  
J Paquette ◽  
P Pannunzio ◽  
S Albrechtson ◽  
K Morgan
Keyword(s):  
Mouse Chromosome ◽  
Regulatory System ◽  
Mutant Gene ◽  
Distal Portion ◽  
Imprinted Genes ◽  
Chromosome 11 ◽  
Lethal Phenotype ◽  
Embryonic Lethal ◽  
Mouse Chromosome 11 ◽  
Gene Maps

Abstract Genome imprinting is the process by which identical alleles at a particular locus may be rendered functionally different depending on the sex of the parent contributing the allele. While several mutations in imprinted genes have been defined, no variants in the regulatory system that gives rise to imprinting have been described. Here we report our genetic analysis of the behavior of the interstrain, polar, embryonic-lethal phenotype known as the "DDK syndrome." We have mapped the interstrain, polar-lethal region of the genome to the distal portion of mouse chromosome 11, near the Xmv-42 locus. We propose that the lethal phenotype is not caused by a standard mutation, but by aberrant imprinting of a gene within this region.

Ileal lipid-binding protein (Illbp) gene maps to mouse Chromosome 11

1994 ◽  
Vol 5 (12) ◽  
pp. 805-806 ◽  
Author(s):  
E. H. Birkenmeier ◽  
L. B. Rowe ◽  
M. W. Crossman ◽  
J. I. Gordon
Keyword(s):  
Mouse Chromosome ◽  
Binding Protein ◽  
Lipid Binding ◽  
Chromosome 11 ◽  
Lipid Binding Protein ◽  
Mouse Chromosome 11 ◽  
Gene Maps

scholarly journals XChromosome Effect on Maternal Recombination and Meiotic Drive in the Mouse

Genetics ◽  
2002 ◽  
Vol 161 (4) ◽  
pp. 1651-1659 ◽  
Author(s):  
Elena de la Casa-Esperón ◽  
J Concepción Loredo-Osti ◽  
Fernando Pardo-Manuel de Villena ◽  
Tammi L Briscoe ◽  
Jan Michel Malette ◽  
...  
Keyword(s):  
Mouse Chromosome ◽  
X Chromosome ◽  
Meiotic Recombination ◽  
Meiotic Drive ◽  
X Chromosome Inactivation ◽  
Chromosome Inactivation ◽  
Chromosome 11 ◽  
Genome Wide ◽  
Mouse Chromosome 11 ◽  
Segregation Of Chromosomes

AbstractWe observed that maternal meiotic drive favoring the inheritance of DDK alleles at the Om locus on mouse chromosome 11 was correlated with the X chromosome inactivation phenotype of (C57BL/ 6-Pgk1a × DDK)F1 mothers. The basis for this unexpected observation appears to lie in the well-documented effect of recombination on meiotic drive that results from nonrandom segregation of chromosomes. Our analysis of genome-wide levels of meiotic recombination in females that vary in their X-inactivation phenotype indicates that an allelic difference at an X-linked locus is responsible for modulating levels of recombination in oocytes.

New testis-specific expressed genes on mouse Chromosome 11

1996 ◽  
Vol 7 (2) ◽  
pp. 163-163
Author(s):  
G. C. Voss ◽  
H. Jockusch
Keyword(s):  
Mouse Chromosome ◽  
Chromosome 11 ◽  
Mouse Chromosome 11
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