| Type | Description |
|---|---|
| Definition | glucosidase, alpha, acid |
| Date | Results | Publications |
|---|---|---|
| 2018-02-10 10:07:00 | the data unequivocally confirm that systemic absence of GAA induces a complex neuropathological cascade in the spinal cord. | 27614205 |
| 2017-08-05 11:47:00 | GAA enzyme deficiency leads to glycogen accumulation in the trachea and bronchi and impairs the ability of lower airway smooth muscle to regulate calcium and respond appropriately to bronchodilator or constrictors. | 28336814 |
| 2015-01-24 10:44:00 | GAA deficiency results in reduced mTORC1 activation that is partly responsible for the skeletal muscle wasting phenotype and can be amerliorated by leucine supplementation. | 25231351 |
| 2012-12-08 10:02:00 | slow glucose release can be induced through the toggling of activities of the mucosal alpha-glucosidases by selective enzyme inhibition | 22851177 |
| 2011-10-22 10:15:00 | Results describe the inhibitory effects of Chana series chalcone derivatives on the activities of alpha-glucosidase and DPP-4, and on adipocyte differentiation. | 21699755 |
| Type | IDs |
|---|---|
| Synonymous | E430018M07Rik |
| Gene |
UniProtKB-ID:
LYAG_MOUSE
UniprotKB:
P70699
UniParc:
UPI0000022679
EMBL:
AK150970,
AK146538,
BC010210,
AK139333,
AK088481,
AK052211,
U49351
Ensembl:
ENSMUSG00000025579
KO:
mmu:14387
|
| Nucleutide sequences |
EMBL-CDS:
BAE30001.1,
BAE27243.1,
BAC34888.1,
BAE23960.1,
AAB06943.1,
BAC40382.1,
AAH10210.1
Ensembl_TRS:
ENSMUST00000026666,
ENSMUST00000106259
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000026666,
ENSMUSP00000101866
RefSeq:
NP_032090.3,
NP_001152796.1
|
| Others |
UniRef100:
UniRef100_P70699
UniRef90:
UniRef90_P70699
UniRef50:
UniRef50_P10253
UniGene:
Mm.4793
CCDS:
CCDS25713.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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