神经发育和其他表型经常与异合体BAZ2B功能丧失变体相关
Soha Sewani1, Mahshid S Azamian1,2, Bryce A Mendelsohn3
1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
American journal of medical genetics. Part A
|October 24, 2023
概括
在BAZ2B基因的功能丧失导致主导神经发育综合征. 这种情况,BAZ2B哈普隆缺陷症,呈现出发育迟缓,智力障碍和明显的身体特征.
科学领域:
- 遗传学 遗传学 是一个
- 神经发育障碍 神经发育障碍
- 染色体生物学 染色体生物学
背景情况:
- BAZ2B基因编码了一种参与基因调节的染色体重塑蛋白.
- 功能丧失的BAZ2B变种被认为会导致神经发育问题和出生缺陷.
- 需要进一步的证据来证实BAZ2B缺陷与观察到的表型之间的联系.
研究的目的:
- 研究BAZ2B哈普隆缺陷在神经发育障碍中的作用.
- 描述与BAZ2B变异相关的临床谱.
- 确认BAZ2B是自体主导神经发育综合征的原因.
主要方法:
- 分析了来自10名携带BAZ2B变异的非相关个体的分子和临床数据.
- 审查之前报告的BAZ2B变异病例.
- 遗传变异分析包括删除,停止增益,移,误解,拼接连接,indel和开始损失.
主要成果:
- 确定了10个具有异合体BAZ2B变异的新无关个体.
- 从轻度受影响或无症状的父母那里观察到遗传,表明穿透不完全.
- 常见的表型包括发育迟缓,智力障碍,自闭症谱系障碍,言语迟缓,发作,视力问题和先天性心脏缺陷.
结论:
- BAZ2B的哈普隆缺陷导致一种自体主导的,不完全透的神经发育综合征.
- 该研究证实BAZ2B变种是发育障碍的原因.
- 关键特征包括神经发育缺陷和特定的形特征,如形和小耳朵.
相关概念视频
Pleiotropy
40.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.5K
Pedigree Analysis
84.4K
Overview
84.4K
Genetic Lingo
102.9K
Overview
102.9K
Incomplete Dominance
22.6K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.6K
Lethal Alleles
15.5K
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...
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...
15.5K


