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In some species, there are hermaphrodites, i.e., individuals that can function reproductively as either female or male. [2] There are also some species in which only one sex is present, temporarily or permanently. This can be due to parthenogenesis, the act of a female reproducing without fertilization.
The idea is instead of having a simplistic mechanism by which you have pro-male genes going all the way to make a male, in fact there is a solid balance between pro-male genes and anti-male genes and if there is a little too much of anti-male genes, there may be a female born and if there is a little too much of pro-male genes then there will ...
In contrast, a female must inherit two mutant alleles, a less frequent event since the mutant allele is rare in the population. X-linked traits are maternally inherited from carrier mothers or from an affected father. Each son born to a carrier mother has a 50% probability of inheriting the X chromosome carrying the mutant allele.
The gender gap in life expectancy suggests differences in the aging process between males and females. A key factor underlying aging is considered to be DNA damage , particularly DNA double-strand breaks, and the capability to repair these damages declines with age. [ 128 ]
In birds and some reptiles, by contrast, it is the female which is heterozygous and carries a Z and a W chromosome while the male carries two Z chromosomes. In mammals, females can have XXX or X. [30] [31] Mammalian females bear live young, with the exception of monotreme females, which lay eggs. [32]
The term may be used as "an umbrella term, encompassing several gender identities, including intergender, agender, xenogender, genderfluid, and demigender." [ 21 ] Some non-binary identities are inclusive , because two or more genders are referenced, such as androgyne/androgynous, intergender, bigender, trigender, polygender, and pangender.
In genetics, a maternal effect occurs when the phenotype of an organism is determined by the genotype of its mother. [1] For example, if a mutation is maternal effect recessive, then a female homozygous for the mutation may appear phenotypically normal, however her offspring will show the mutant phenotype, even if they are heterozygous for the mutation.
There are fewer X-linked dominant conditions than X-linked recessive, because dominance in X-linkage requires the condition to present in females with only a fraction of the reduction in gene expression of autosomal dominance, since roughly half (or as many as 90% in some cases) of a particular parent's X chromosomes are inactivated in females.
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