Human (GRCh37.p13)
Description

amelogenin, X-linked [Source:HGNC Symbol;Acc:461]

Gene Synonyms

AI1E, AIH1, ALGN, AMG, AMGL, AMGX

Location

Chromosome X: 11,311,533-11,318,881 forward strand.

GRCh37:CM000685.1

About this gene

This gene has 3 transcripts (splice variants), 1 paralogue and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380712.3AMELX-002835205aaENSP00000370088.3
 
Protein coding
CCDS14145B2BY28 Q99217 NM_182680.1GENCODE basic
ENST00000380714.3AMELX-001793191aaENSP00000370090.3
 
Protein coding
CCDS14144B2BY28 Q99217 NM_001142.2GENCODE basic
ENST00000348912.4AMELX-201737175aaENSP00000335312.5
 
Protein coding
CCDS14146B2BY28 Q99217 NM_182681.1GENCODE basic

Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.