Protein Domain : AmmeMemoRadiSam system protein A IPR027623

Type  Family
Description  Members of this protein family belong to the same domain family as AMMECR1 , a mammalian protein whose deficit is involved in the association of Alport syndrome, midface hypoplasia, intellectual disability and elliptocytosis in humans [ ]. Members of the present family occur as part of a three gene system with a homologue of the mammalian protein Memo (Mediator of ErbB2-driven cell MOtility), and an uncharacterised radical SAM enzyme [].
Short Name  AmmeMemoSam_A

0 Child Features

0 Gene Families

0 Genes

0 Ontology Annotations

1 Parent Features

0 Publications

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