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15号染色体开放阅读框41抗体
半岛bd体育手机客户端 介绍
靶标:
CDIN1 半岛bd体育手机客户端 别名: C15orf41; HH114; CDIN1; CDAN1 interacting nuclease 1; CDAN1 interacting nuclease 1; CDAN1-interacting nuclease 1; protein C15orf41; uncharacterized protein C15orf41; 15号染色体开放阅读框41; 背景信息:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The C15orf41 gene product has been provisionally designated C15orf41 pending further characterization.
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