Health / Medical Topics |
PLP1 wt Allele
Human PLP1 wild-type allele is located in the vicinity of Xq22 and is approximately 16 kb in length. This allele, which encodes myelin proteolipid protein, plays a role in the modulation of neuronal development and function. Mutation of the gene is associated with both Pelizaeus-Merzbacher disease and spastic paraplegia type 2. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene is involved in neuronal development.
A computer driven instrument designed for drawing graphs and pictures.
The number of sets of chromosomes in a cell or an organism. For example, haploid means one set and diploid means two…
A type of chronic lymphocytic leukemia (CLL) in which too many immature white blood cells (prolymphocytes) are found in the blood and…
Human PLK3 wild-type allele is located in the vicinity of 1p34.1 and is approximately 6 kb in length. This allele, which encodes…
This gene is involved in the regulation of mitosis.