AMMECR1 抗体
(Alport Syndrome, Mental Retardation, Midface Hypoplasia and Elliptocytosis Chromosomal Region Gene 1 (AMMECR1))
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. [provided by RefSeq, Jan 2010].
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Aliases for AMMECR1 抗体
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 L homeolog (ammecr1.L) 抗体Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (AMMECR1) 抗体
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (Ammecr1) 抗体
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 (ammecr1) 抗体
6230420G18Rik 抗体
AMMECR1 抗体
Ammecr1 抗体
ammerc1 抗体
AMMERC1 抗体
MGC84095 抗体
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