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関連する概念動画

Genetic Lingo01:11

Genetic Lingo

112.9K
Overview
112.9K
Lethal Alleles02:41

Lethal Alleles

17.4K
Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
17.4K
Epistasis Analysis01:09

Epistasis Analysis

5.5K
Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
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Multiple Allele Traits01:49

Multiple Allele Traits

37.6K
The Concept of Multiple Allelism
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Probability Laws01:49

Probability Laws

43.5K
Overview
43.5K
Hardy-Weinberg Principle01:49

Hardy-Weinberg Principle

75.6K
Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.
75.6K

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関連する実験動画

Updated: Dec 12, 2025

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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アレル制約:多因子の値遺伝に対する生物学的代替手段.

M Melnick, E D Shields

    Lancet (London, England)
    |January 24, 1976
    PubMed
    まとめ

    アレル制限モデルは,保守的な多因子値モデルとは異なり,一般的な先天性不形成に関する新しい洞察を提供します. palatal cleft の集団データは,この遺伝的仮説を裏付けている.

    科学分野:

    • 遺伝学 遺伝学とは
    • 発達生物学 発達生物学について
    • ヒューマン・バイオロジー ヒューマン・バイオロジー

    背景:

    • 生まれつきの変形に対する多要素値モデルには,生物学的洞察が欠けている.
    • 現在のモデルは,複雑な数学的仮定に依存しています.
    • 共通の先天性不形成の遺伝を説明するために,新しいモデルが必要である.

    研究 の 目的:

    • 共通のヒト先天性不形成の発生に"アレル制限"モデルを適用する.
    • これらの疾患の遺伝的根拠を理解するための新しい枠組みを提供すること.

    主な方法:

    • 隔離された口腔裂け目の新しい集団データを活用する.
    • このデータの"アレル制限"モデルの予測に適合するかを分析する.

    主要な成果:

    • 隔離された裂口口の集団データは",アレル制限"モデルに密接に適合しています.
    • このモデルは,一般的な先天性不形成の遺伝的症例において,浸透率の低下を説明する.
    • このモデルは,高周波と限られた垂直伝送の条件に適用できます.

    結論:

    さらに関連する動画

    Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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    An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
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    An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

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    Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
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    An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
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    An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

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  • "アレル制限"モデルは,一般的な先天性不形成の生物学的に妥当な説明を提供します.
  • このモデルは,異質性,フェノコピー,および減少した浸透性を説明します.
  • それは,多要素的値モデルの限界に対する価値ある代替案を提供します.