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Albright syndrome is caused by a mutation in a gene that is imprinted. A is the wild-type allele and a is the mutant allele. A star (*) represents imprinting (methylation). The pedigree below shows a family with a history of Albright syndrome, and some of the genotypes of the first generation are labeled.

Albright syndrome is caused by a mutation in a gene that is imprinted. A is the wild-type allele and a is the mutant allele. A star (*) represents imprinting (methylation). The pedigree below shows a family with a history of Albright syndrome, and some of the genotypes of the first generation are labeled.

Human Anatomy & Physiology (11th Edition)
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
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Albright syndrome is caused by a mutation in a gene that is imprinted. A is the wild-type allele and a is the mutant allele. A star (*) represents imprinting (methylation). The pedigree below shows a family with a history of Albright syndrome, and some of the genotypes of the first generation are labeled. aa* Aa* AA* I. 1 3 4 II. 1 2 3 4 III.
Transcribed Image Text:Albright syndrome is caused by a mutation in a gene that is imprinted. A is the wild-type allele and a is the mutant allele. A star (*) represents imprinting (methylation). The pedigree below shows a family with a history of Albright syndrome, and some of the genotypes of the first generation are labeled. aa* Aa* AA* I. 1 3 4 II. 1 2 3 4 III.
What is individual II-4's genotype? Indicate imprinting with a star (*).
Transcribed Image Text:What is individual II-4's genotype? Indicate imprinting with a star (*).
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