免 疫 原：KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58
抗原表位：301-385/385
SWISS：Q6ZNW5
Gene ID ：390637
Human Gene ID：390637

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 LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
Function：Specific and highly efficient GDP-D-glucose phosphorylase regulating the levels of GDP-D-glucose in cells.
Subcellular Location：Cytoplasm.
Similarity：Belongs to the GDPGP1 family.
Important Note：This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.