AP BIOLOGY

CELL DIVISION

MEIOSIS

Question [CLICK ON ANY CHOICE TO KNOW THE RIGHT ANSWER]
What is the genotype for a male human (boy)?
A
XX
B
XY
Explanation: 

Detailed explanation-1: -Genotypic sex refers specifically to an individual’s two sex chromosomes. Most people have either two X chromosomes (genotypic female) or an X and a Y chromosome (genotypic male).

Detailed explanation-2: -The X and Y chromosomes, also known as the sex chromosomes, determine the biological sex of an individual: females inherit an X chromosome from the father for a XX genotype, while males inherit a Y chromosome from the father for a XY genotype (mothers only pass on X chromosomes).

Detailed explanation-3: -The twenty third pair is called the sex chromosomes, while the rest of the 22 pairs are called autosomes. Typically, biologically male individuals have one X and one Y chromosome (XY) while those who are biologically female have two X chromosomes.

Detailed explanation-4: -Usually, a female baby has 2 X chromosomes (XX) and a male has 1 X and 1 Y (XY). But in Klinefelter syndrome, a boy is born with an extra copy of the X chromosome (XXY). The X chromosome is not a “female” chromosome and is present in everyone. The presence of a Y chromosome denotes male sex.

Detailed explanation-5: -Males with XYY syndrome have 47 chromosomes because of the extra Y chromosome. This condition is also sometimes called Jacob’s syndrome, XYY karyotype, or YY syndrome.

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