| Primary Identifier | IPR027485 | Type | Homologous_superfamily |
| Short Name | AMMECR1_N |
| description | This entry represents an N-terminal subdomain of the AMMECR1 domain (). It consists of a 2-layer sandwich structure. Defects in Nuclear protein AMMECR1 (AMMECR1) are involved association of Alport syndrome, midface hypoplasia, intellectual disability and elliptocytosis in humans []. |
