Tags: Protein.
In mollecular biology the AMMECR1 protein (Alport syndrome intellectual disability midface hypoplasia and elliptocytosis chromosomal region gene 1 protein) is a protein encoded by the AMMECR1 gene on human chromosome Xq22.3. The contiguous gene deletion syndrome is characterised by Alport syndrome (A) intellectual disability (M) midface hypoplasia (M) and elliptocytosis (E) as well as generalized hypoplasia and cardiac abnormalities.
