Homologous Superfamily

AMMECR1, N-terminal (IPR027485)

Short name: AMMECR1_N

Overlapping entries


This entry represents an N-terminal subdomain of the AMMECR1 domain (IPR002733). It consists of a 2-layer sandwich structure. Defects in AMME syndrome candidate gene 1 protein (AMMECR1) are involved in Alport syndrome (A) with mental retardation (M) midface hypoplasia (M) and elliptocytosis (E).

Contributing signatures

Signatures from InterPro member databases are used to construct an entry.