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  2. Pleiotropy - Wikipedia

    en.wikipedia.org/wiki/Pleiotropy

    G1, G2, and G3 are different genes that contribute to phenotypic traits P1, P2, and P3. Pleiotropy (from Greek πλείων pleion, 'more', and τρόπος tropos, 'way') occurs when one gene influences two or more seemingly unrelated phenotypic traits. Such a gene that exhibits multiple phenotypic expression is called a pleiotropic gene.

  3. Position effect - Wikipedia

    en.wikipedia.org/wiki/Position_effect

    Position effect is the effect on the expression of a gene when its location in a chromosome is changed, often by translocation. This has been well described in Drosophila with respect to eye color and is known as position effect variegation (PEV). [1] The phenotype is well characterised by unstable expression of a gene that results in the red ...

  4. Position-effect variegation - Wikipedia

    en.wikipedia.org/wiki/Position-effect_variegation

    The effect is the variegation in a particular phenotype i.e., the appearance of irregular patches of different colour(s), due to the expression of the original wild-type gene in some cells of the tissue but not in others, [8] as seen in the eye of mutated Drosophila melanogaster.

  5. Congenital red–green color blindness - Wikipedia

    en.wikipedia.org/wiki/Congenital_red–green...

    The third gene array shows a deuteranopia genotype; the fourth shows a normal color vision genotype. When unequal recombination happens with breaks between the genes (depicted by blue lines), a gene can be essentially deleted from one of the chromosomes. This gene deletion leads to protanopia or deuteranopia (congenital red–green dichromacy).

  6. Ciliopathy - Wikipedia

    en.wikipedia.org/wiki/Ciliopathy

    A ciliopathy is any genetic disorder that affects the cellular cilia or the cilia anchoring structures, the basal bodies, [1] or ciliary function. [2] Primary cilia are important in guiding the process of development, so abnormal ciliary function while an embryo is developing can lead to a set of malformations that can occur regardless of the particular genetic problem. [3]

  7. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Human genetics is the study of inheritance as it occurs in human beings.Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.

  8. Visual system - Wikipedia

    en.wikipedia.org/wiki/Visual_system

    Vision is often one of the first senses affected by aging. A number of changes occur with aging: Over time, the lens becomes yellowed and may eventually become brown, a condition known as brunescence or brunescent cataract. Although many factors contribute to yellowing, lifetime exposure to ultraviolet light and aging are two main causes.

  9. Neuropathy, ataxia, and retinitis pigmentosa - Wikipedia

    en.wikipedia.org/wiki/Neuropathy,_ataxia,_and...

    Neuropathy, ataxia, and retinitis pigmentosa, also known as NARP syndrome, is a rare disease with mitochondrial inheritance that causes a variety of signs and symptoms chiefly affecting the nervous system [1] Beginning in childhood or early adulthood, most people with NARP experience numbness, tingling, or pain in the arms and legs (sensory neuropathy); muscle weakness; and problems with ...