ALG1L2
Description
The ALG1L2 (ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase like 2) is a protein-coding gene located on chromosome 3.
ALG1L2 is thought to be a glycosyltransferase, an enzyme that transfers sugar molecules to other molecules.
ALG1L2 is also known as -.
Associated Diseases
- neutrophil immunodeficiency syndrome
- linear and whorled nevoid hypermelanosis
- transient myeloproliferative syndrome
- primary immunodeficiency syndrome due to p14 deficiency
- neutropenia, severe congenital, 1, autosomal dominant
- muscular dystrophy
- ichthyosis prematurity syndrome
- uncombable hair syndrome
- eosinophil peroxidase deficiency
- thrombocytopenia 2
- Griscelli syndrome type 2
