Health / Medical Topics |
DES wt Allele
Human DES wild-type allele is located in the vicinity of 2q35 and is approximately 8 kb in length. This allele, which encodes desmin protein, plays a role in muscle cell contraction. Mutation of the gene is associated with myopathy myofibrillar desmin-related, cardiomyopathy dilated type 1I and neurogenic scapuloperoneal syndrome Kaeser type. (NCI Thesaurus)
YOU MAY ALSO LIKE
This gene is involved in the maintenance of muscle cell structure.
A synthetic form of the hormone estrogen that was prescribed to pregnant women between about 1940 and 1971 because it was thought…
A type of benign (not cancer) germ cell tumor (type of tumor that begins in the cells that give rise to sperm…
Dermoid; resembling skin; skinlike.
The inner layer of the two main layers of the skin. The dermis has connective tissue, blood vessels, oil and sweat glands,…
A benign skin condition commonly seen in dark-skinned individuals that is characterized by multiple small hyperpigmented papular lesions resembling seborrheic keratosis on…