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AMMECR1
AMMECR nuclear protein 1The 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]
Top validated antibodies |
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| Proteintech Group |  24687-1-AP |
Polyclonal |
WB
EL
IHC
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| NovoPro Bioscience Inc. | 107996 |
Polyclonal |
WB
EL
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA22559A0Rb |
Polyclonal |
EL
ICC
IHC
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| FineTest Biotech | FNab00364 |
Polyclonal |
WB
EL
IHC
|
||
| Invitrogen Antibodies | 24687-1-AP |
Polyclonal |
WB
IHC
|
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