Type | Description |
---|---|
Definition | family with sequence similarity 83, member H |
Date | Results | Publications |
---|---|---|
2020-05-30 12:57:00 | Fam83h-/- mice showed no enamel phenotype. Fam83h Tr/Tr (p.Tyr297*) mutation disturbed amelogenesis through a neomorphic mechanism and caused obvious enamel malformations. | 31060110 |
2019-08-17 11:41:00 | These findings shed new light on the association of Fam83h and fluorosis and indicated that high fluoride decreased the expression of Fam83h in morphological and cytological development. This may be one of the reasons for the occurrence of fluorosis. | 29676651 |
2018-10-13 10:18:00 | Compared with the control, the Fam83h mutation altered the expression and localization of Fam83h, CK1alpha and beta-catenin in LS8 ameloblasts, inhibited mineralization and down-regulated the expression of mineralization factors. | 29709481 |
2014-04-26 12:30:00 | Findings demonstrate that over-expression of FAM83H in mice does not produce a phenotype in dentine or enamel. | 23545224 |
Type | IDs |
---|---|
Synonymous | AA409316 |
Gene |
UniProtKB-ID:
FA83H_MOUSE
UniprotKB:
Q148V8
UniParc:
UPI00001C5817
EMBL:
AK035531,
BC023045,
BC117948,
BC117947,
BC036149,
BC022937
Ensembl:
ENSMUSG00000046761
KO:
mmu:105732
|
Nucleutide sequences |
EMBL-CDS:
BAC29093.1,
AAI17949.1,
AAI17948.1,
AAH22937.1,
AAH36149.1,
AAH23045.1
Ensembl_TRS:
ENSMUST00000170153,
ENSMUST00000060807
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000126453,
ENSMUSP00000059839
RefSeq:
NP_001161725.1,
XP_006520299.3,
XP_006520300.1,
NP_598848.2
|
Others |
UniRef100:
UniRef100_Q148V8
UniRef90:
UniRef90_Q148V8
UniRef50:
UniRef50_Q6ZRV2
UniGene:
Mm.267178
CCDS:
CCDS27559.1
|
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