ammecr1
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  • Official Full Name
  • Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
  • Background
  • The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
  • Synonyms
  • AMMECR1; Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1; AMME syndrome candidate gene 1 protein; Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region gene 1; AMMECR 1; AMMECR1 protein; AMMERC1; OTTHUMP00000023851
Cat.#:AMMECR1-526HTag:GST
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human AMMECR1 protein, GST-tagged
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Cat.#:AMMECR1-9620HTag:His
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human AMMECR1, His-tagged
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Cat.#:AMMECR1-10859ZTag:His
Source (Host):Mammalian CellsSpecies:Zebrafish
Product nameRecombinant Zebrafish AMMECR1
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Cat.#:AMMECR1-8880HCLTag:
Source (Host):Species:Human
Product nameRecombinant Human AMMECR1 293 Cell Lysate
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