Type | Description |
---|---|
Definition | amelogenin X-linked |
Date | Results | Publications |
---|---|---|
2020-07-18 11:39:00 | family study of a novel AMELX mutation with skewed X chromosome inactivation causing hypoplastic and hypomineralized amelogenesis imperfecta | 31185186 |
2020-02-08 10:52:00 | AMELX and ODAM variations was not different between two populations of schoolchildren with respect to dental fluorosis (DF) severity; however, the presence of rs1784418 differed between phenotypes with regard to susceptibility to DF. Therefore, MMP20 might be related to the various phenotypes of DF | 31838295 |
2018-10-20 10:19:00 | High AMEL expression is associated with Aggressiveness in Odontogenic Tumors. | 29802703 |
2018-09-08 12:10:00 | Single nucleotide polymorphisms in the AMELX and AMBN genes may be genetic variants that contribute to developmental defects of enamel in primary dentition of Polish children. | 28382465 |
2018-07-14 12:01:00 | To the best of our knowledge, this is the first report of expression of human amelogenin in plants, offering the possibility to use this plant-made protein for nanotechnological applications. | 28801830 |
Type | IDs |
---|---|
Synonymous | AI1E, AIH1, ALGN, AMG, AMGL, AMGX |
Gene |
UniProtKB-ID:
AMELX_HUMAN
UniprotKB:
Q99217
UniParc:
UPI000002A3B7,
UPI000012596C,
UPI000002A3B6
EMBL:
M55418,
X14440,
AF436849,
AY040206,
M86932,
S67147,
AC002366,
BC074951
Ensembl:
ENSG00000125363
KO:
hsa:265
|
Nucleutide sequences |
EMBL-CDS:
CAA32613.1,
AAA51717.1,
AAL30432.1,
AAA62826.1,
AAC21581.1,
AAB29184.1,
AAK77213.1,
AAH74951.1
Ensembl_TRS:
ENST00000380714,
ENST00000348912,
ENST00000380712
|
Protein sequencees |
Ensembl_PRO:
ENSP00000335312,
ENSP00000370088,
ENSP00000370090
RefSeq:
XP_016884893.1,
NP_872621.1,
NP_001133.1,
NP_872622.1
|
Others |
UniRef100:
UniRef100_Q99217
UniRef90:
UniRef90_Q99217
UniRef50:
UniRef50_Q99217
UniGene:
Hs.654436
CCDS:
CCDS14146.1,
CCDS14145.1,
CCDS14144.1
|
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Refseq |
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