Ontology highlight
ABSTRACT:
SUBMITTER: Ahmed MS
PROVIDER: S-EPMC6077826 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature
Ahmed Md Shakil MS Shahjaman Md M Kabir Enamul E Kamruzzaman Md M
Bioinformation 20180531 5
The dyserythropoietic anemia disease is a genetic disorder of erythropoiesis characterized by morphological abnormalities of erythroblasts. This is caused by human gene C15orf41 mutation. The uncharacterized C15orf41 protein is involved in the formation of a functional complex structure. The uncharacterized C15orf41 protein is thermostable, unstable and acidic. This is associated with TPD (Treponema Pallidum) domain (135 to 265 residue position) and three PTM sites such as K50 (Acetylation), T11 ...[more]