AMELY
Description
The AMELY (amelogenin Y-linked) is a protein-coding gene located on chromosome Y.
Amelogenin, Y isoform is a protein encoded by the AMELY gene, located on the Y chromosome. This gene produces a form of amelogenin, an extracellular matrix protein involved in biomineralization during tooth enamel development. Mutations in the related AMELX gene on the X chromosome can cause X-linked amelogenesis imperfecta.
AMELY is also known as AMGL, AMGY.
Associated Diseases
- dentin dysplasia type I
- amelogenesis imperfecta hypomaturation type 2A4
- amelogenesis imperfecta, IIa 1K
- amelogenesis imperfecta type 3B
- dentin dysplasia type II
- amelogenesis imperfecta
- dentinogenesis imperfecta type 3
- hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
- trichodysplasia-amelogenesis imperfecta syndrome
- amelogenesis imperfecta, type 3A
- tooth agenesis, selective, 7
- dentin dysplasia-sclerotic bones syndrome
- otodental syndrome
- hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome
- fused mandibular incisors
- dentin dysplasia
- Ackerman syndrome
