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FAP follows both an autosomal recessive and autosomal dominant pattern depending on which gene you inherit the disease from. If inherited through the APC gene, which is most common, it is autosomal gdthe disease. If inherited through the MUTYH gene it is autosomal recessive, meaning that both parents were carriers of the disease or they both were living with the disease.
Let's take red-green color vision as an example. You could use the letter n to represent the dominant and recessive alleles. You could use a capital letter N to represent the normal allele, which is dominant, and a lowercase letter n to represent the defective allele, which is recessive. The genotypes for the sex-linked trait would be as follows: female, homozygous dominant: XNXN; female, heterozygous: XNXn; male dominant, XNY; male recessive, XnY.
Gregor Johann Mendel was a German speaking Austrian Augustinian priest and scientist, and is often called the father of genetics for his study of the inheritance of traits in pea plants. Mendel showed that the inheritance of traits follows particular laws, which were later named after him. The significance of Mendel's work was not recognized until the turn of the 20th century. Its rediscovery prompted the foundation of the discipline of genetics.
The three fundamental elements of mendelism are his three theories of inheritance. these are as follows. 1. law of dominance 2. law of segregation 3. law of independent assortment.
Mendel was considered as the father of genetics because he showed that inheritance follows certain patterns. He was famous for working with pea plants. He bred different kinds of pea plants to get particular traits, such as tall or short.
Sex-linked - Colorblindness Autosomal Dominant - Huntington's disease Autosomal Recessive - Tay Sach's
This type of inheritance represents alleles at the same locus where one is recessive to the other. The dominant phenotype occurs in all heterozygous offspring as well as the homozygous dominant offspring. This yields a 3:1 phenotype and a 1:2:1 genotype.
FAP follows both an autosomal recessive and autosomal dominant pattern depending on which gene you inherit the disease from. If inherited through the APC gene, which is most common, it is autosomal gdthe disease. If inherited through the MUTYH gene it is autosomal recessive, meaning that both parents were carriers of the disease or they both were living with the disease.
Pancreatic cancer is not caused by a single gene mutation that follows typical dominant or recessive inheritance patterns. Instead, it is usually the result of multiple genetic and environmental factors interacting over time. Some inherited genetic mutations, such as those in the BRCA1 and BRCA2 genes, can increase the risk of pancreatic cancer, but they do not follow a simple dominant or recessive pattern.
Let's take red-green color vision as an example. You could use the letter n to represent the dominant and recessive alleles. You could use a capital letter N to represent the normal allele, which is dominant, and a lowercase letter n to represent the defective allele, which is recessive. The genotypes for the sex-linked trait would be as follows: female, homozygous dominant: XNXN; female, heterozygous: XNXn; male dominant, XNY; male recessive, XnY.
Tay-Sachs is an autosomal (not sex linked) recessive disorder which has no effects at birth but leads to blindness, paralysis, mental retardation and death by three to four years of age.i have tay sachs and i am dead HAHA WORL SUK IT
Mendal learned that there are two kinds of traits,,dominate and recessive. He also learned that the enheritance of the traits are determined by genes.
a pedigree
If short hair, represented by L, is the dominant trait, then both animals with LL genes and Ll genes will have short hair because they have the short hair gene. The Ll animal, however, may have a long haired offspring if they mate with another animal carrying the long hair gene and they both pass it on.
It is an exception to Mendel's Laws of Inheritance and follows a pattern of co-dominance.
In genetics, homozygous genes are identical alleles, while heterozygous genes have different alleles. For example, TT(same alleles) is homozygous genotype, while Tt (different alleles) is a heterozygous genotype.
First, meiosis independently assorts chromosomes when gametes are made for sexual reproduction and second, human heredity involves the same relationsips between alleles-dominant and recessive interactions, polygenic traits, and sex-linked genes.