Congenital pulmonary alveolar proteinosis is a rare lung disease in humans. The disease is caused by a recessive mutation in the gene CSF2RA. CSF2RA is located within a pseudoautosomal region of the X and Y chromosomes. The normal allele is notated as Cnorm, and the mutant allele is notated as Cmut. Suppose that a woman with Cnorm on both X chromosomes (XCnormyCnorm) has children with a man with Cmut on the X chromosome and Cnorm on the Y chromosome (XCmut yCnorm. Select all possible genotypes of their offspring Select all possible genotypes of their offspring for males. for females. OXCmurmx Cmut O x Cmuty Cmat O xCmuty Cmut XCnormy Cmut X CRormy Cnurm XChormyCnorm XCmuty Cnorm
Congenital pulmonary alveolar proteinosis is a rare lung disease in humans. The disease is caused by a recessive mutation in the gene CSF2RA. CSF2RA is located within a pseudoautosomal region of the X and Y chromosomes. The normal allele is notated as Cnorm, and the mutant allele is notated as Cmut. Suppose that a woman with Cnorm on both X chromosomes (XCnormyCnorm) has children with a man with Cmut on the X chromosome and Cnorm on the Y chromosome (XCmut yCnorm. Select all possible genotypes of their offspring Select all possible genotypes of their offspring for males. for females. OXCmurmx Cmut O x Cmuty Cmat O xCmuty Cmut XCnormy Cmut X CRormy Cnurm XChormyCnorm XCmuty Cnorm
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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Transcribed Image Text:XCrx Ct
XCmary Cmut
XCormy Caorm
XCnormy Cmut
XChormy Cnorm
XCmuty Chorm
Which genotype is associated with the disease phenotype for pulmonary alveolar proteinosis?
ONone of these.
XCaormy Cmut
XCmaty Cnorm
XCormy Cmut

Transcribed Image Text:Congenital pulmonary alveolar proteinosis is a rare lung disease in humans. The disease is caused by a recessive mutation in the
gene CSF2RA. CSF2RA is located within a pseudoautosomal region of the X and Y chromosomes. The normal allele is notated
as Cnorm, and the mutant allele is notated as Cmut.
Suppose that a woman with Cnorm on both X chromosomes (XCnormyCnor) has children with a man with Cmut on the X
chromosome and Cnorm on the Y chromosome (XCmut yCnorm).
.Select all possible genotypes of their offspring
Select all possible genotypes of their offspring for males.
for females.
OXCnormx Cmut
O
XCmury Cmut
XCmutX Cmut
OXCRormy Cmut
XCnurmy Cnorm
OX Chormy Cnorm
OXCury Chorp
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