Type | Description |
---|---|
Definition | cytidine monophospho-N-acetylneuraminic acid hydroxylase |
Date | Results | Publications |
---|---|---|
2020-04-04 11:16:00 | Human evolutionary loss of CMAH likely contributes to atherosclerosis predisposition via multiple intrinsic and extrinsic mechanisms. | 31332008 |
2017-12-30 12:41:00 | These findings have the potential to significantly advance our understanding of how this enigmatic tumor-associated antigen is produced in humans, and also suggest a possible mechanism of action of anti-tumor antibodies that recognize hypoxia markers, such as 14F7. | 29196263 |
2017-09-16 11:20:00 | this study shows that Cmah(-/-) mice manifest a decreased survival in endotoxemia following bacterial lipopolysaccharide injection, and that macrophages from Cmah(-/-) mice secrete more inflammatory cytokines with LPS stimulation and show more phagocytic activity | 28148732 |
2016-09-03 10:58:00 | Used CMP-Neu5Ac Hydroxylase null mouse models to study the modification/turnover of gene products that are altered in humans due to evolutionary loss of Neu5Gc. | 26558285 |
2016-05-21 11:53:00 | The target miRNAs are closely associated with dysregulation of insulin/PI3K-AKT signaling, suggesting that the Cmah-null mice could be a useful model for studying diabetes. | 25243123 |
Type | IDs |
---|---|
Gene |
UniProtKB-ID:
CMAH_MOUSE
UniprotKB:
Q61419
UniParc:
UPI000050AAD9,
UPI0000028630
EMBL:
BC055079,
AB061346,
D21826,
AB061276,
AB061277,
AL589744
Ensembl:
ENSMUSG00000016756
KO:
mmu:12763
|
Nucleutide sequences |
EMBL-CDS:
AAH55079.1,
BAB91361.1,
BAB91362.1,
BAB91553.1,
BAA04850.1
Ensembl_TRS:
ENSMUST00000224657,
ENSMUST00000110391,
ENSMUST00000050859,
ENSMUST00000224953,
ENSMUST00000167746
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000061045,
ENSMUSP00000153652,
ENSMUSP00000153495,
ENSMUSP00000129007,
ENSMUSP00000106021
RefSeq:
XP_011242568.1,
XP_011242567.1,
XP_036013735.1,
NP_001104580.1,
NP_001271449.1,
XP_011242576.1,
NP_001271448.1,
NP_031743.3
|
Others |
UniRef100:
UniRef100_Q61419
UniRef90:
UniRef90_Q61419
UniRef50:
UniRef50_Q61419
UniGene:
Mm.8396
CCDS:
CCDS26376.1
|
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