Protein Domain : AMMECR1, N-terminal IPR027485

Type  Homologous_superfamily
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 [ ].
Short Name  AMMECR1_N
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0 Child Features

1 Gene Families

Trail: ProteinDomain

105 Genes

Trail: ProteinDomain

0 Ontology Annotations

0 Parent Features

14 Publications

Trail: ProteinDomain
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