| Primary Identifier | IPR027623 | Type | Family |
| Short Name | AmmeMemoSam_A |
| 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 []. |
