2017-5-4
英文名称 Anti-C9orf6
中文名称 9号染色体开放阅读框6抗体
别 名 CG 8; CG8; FLJ20457; Hypothetical protein LOC54942; UPF0436 protein C9orf6; F206A_HUMAN.
详细介绍:
相关资料:
产品介绍 Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf6 gene product has been provisionally designated C9orf6 pending further characterization.
Similarity : Belongs to the FAM206 family.
Database links : UniProtKB/Swiss-Prot: Q9NX38.1
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