| 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 [ ]. | Name | AMMECR1, N-terminal |
| Short Name | AMMECR1_N | Type | Homologous_superfamily |
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