AMELX
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amelogenin (amelogenesis imperfecta 1, X-linked)
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| Identifiers | |
| Symbol | AMELX AMG, AIH1 |
| HUGO | 461 |
| Entrez | 265 |
| OMIM | 300391 |
| RefSeq | NM_001142 |
| UniProt | Q99217 |
| Other data | |
| Locus | Chr. X p22.3-p22.1 |
AMELX is a form of amelogenin found on the X chromosome.
Mutations in AMELX can cause amelogenesis imperfecta, a disorder of tooth enamel development.
[edit] See also
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