重组22号染色体开放阅读框32蛋白
交货期：1周
产品别名：重组天冬氨酸丰富尾单跨膜蛋白1(SMDT1)
Recombinant Smdt1
Recombinant Smdt1
基因名：
产品别名：
背景信息：
Smdt1
产品别名：
1500032L24Rik； Emre； Smdt1； single-pass membrane protein with aspartate rich tail 1； single-pass membrane protein with aspartate rich tail 1； essential MCU regulator, mitochondrial； UPF0466 protein C22orf32 homolog, mitochondrial； single-pass membrane protein with aspartate-rich tail 1, mitochondrial； 22号染色体开放阅读框32； 天冬氨酸丰富尾单跨膜蛋白1(SMDT1)；
背景信息：
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf32 gene product has been provisionally designated C22orf32 pending further characterization
产品发布日期：2026.03.20
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