NEET BIOLOGY

GENETICS AND EVOLUTION

INHERITANCE AND VARIATION

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
What would the genotype Aa be termed as?
A
Heterozygous
B
Homozygous Dominant
C
Homozygous Recessive
D
None of the above
Explanation: 

Detailed explanation-1: -The presence of two different alleles at a single locus is known as a heterozygous genotype. Each individual carries two variations of gene one from the biological mother and the second from the biological father.

Detailed explanation-2: -(HEH-teh-roh-ZY-gus JEE-noh-tipe) The presence of two different alleles at a particular gene locus. A heterozygous genotype may include one normal allele and one mutated allele or two different mutated alleles (compound heterozygote).

Detailed explanation-3: -Heterozygous refers to having different alleles for a particular trait. If the two versions are different, you have a heterozygous genotype for that gene.

Detailed explanation-4: -This is the case with Huntington disease, achondroplastic dwarfism, and polydactyly. People who are heterozygous (Aa) are not healthy carriers. They have the disorder just like homozygous dominant (AA) individuals. of being entirely normal.

Detailed explanation-5: -If an organism has two copies of the same allele, for example AA or aa, it is homozygous for that trait. If the organism has one copy of two different alleles, for example Aa, it is heterozygous.

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