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AMELY

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This is an old revision of this page, as edited by SimLibrarian (talk | contribs) at 03:48, 4 June 2023 (Changing short description from "Protein-coding gene in the species Homo sapiens" to "Protein-coding gene in humans"). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

AMELY
Identifiers
AliasesAMELY, AMGL, AMGY, amelogenin, Y-linked, amelogenin Y-linked
External IDsOMIM: 410000; MGI: 88005; HomoloGene: 47996; GeneCards: AMELY; OMA:AMELY - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001143
NM_001364814

NM_001081978
NM_009666
NM_001290371

RefSeq (protein)

NP_001134
NP_001351743

NP_001075447
NP_001277300
NP_033796

Location (UCSC)Chr Y: 6.87 – 6.91 MbChr X: 167.96 – 167.97 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Amelogenin, Y isoform is a protein that in humans is encoded by the AMELY gene.[5][6] AMELY is located on the Y chromosome and encodes a form of amelogenin. Amelogenin is an extracellular matrix protein involved in biomineralization during tooth enamel development.

Clinical significance

Mutations in the related AMELX gene on the X chromosome cause X-linked amelogenesis imperfecta.[6]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000099721Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000031354Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Nakahori Y, Takenaka O, Nakagome Y (February 1991). "A human X-Y homologous region encodes "amelogenin"". Genomics. 9 (2): 264–9. doi:10.1016/0888-7543(91)90251-9. PMID 2004775.
  6. ^ a b "Entrez Gene: amelogenin".

Further reading