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Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The KIAA0562 gene product has been provisionally designated KIAA0562 pending further characterization.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: centrosomal protein 104kDa; Centrosomal protein of 104 kDa; Cep104; Gly-, L-Glu and TCP-binding protein; Glycine-, glutamate- and thienylcyclohexylpiperidine-binding protein; glycine-, glutamate-, thienylcyclohexylpiperidine-binding protein; likely ortholog of H. sapiens glycine-, glutamate-, thienylcyclohexylpiperidine-binding protein
基因别名: A930027E11; AI115523; CEP104; CFAP256; GlyBP; JBTS25; KIAA0562; mKIAA0562; ROC22
UniProt ID: (Human) O60308, (Rat) D3Z8X7, (Mouse) Q80V31
Entrez Gene ID: (Human) 9731, (Rat) 246295, (Mouse) 230967