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12763 Cmah

12763

Cmah

cytidine monophospho-N-acetylneuraminic acid hydroxylase

protein-coding

Mus musculus

基因描述

Type Description
Definition cytidine monophospho-N-acetylneuraminic acid hydroxylase

研究结论

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

名称对应

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

全选

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