Type | Description |
---|---|
Definition | galactosidase, alpha |
Date | Results | Publications |
---|---|---|
2016-12-31 10:42:00 | Mice with alpha-galactosidase A deficiency show age-dependent and distinct deficits of the sensory system. | 27145802 |
2015-11-28 11:17:00 | The histological changes in Gla KO mice better resemble the type 2 later-onset phenotype observed in patients with residual alpha-galactosidase A activity. | 25553976 |
2015-07-04 15:24:00 | our findings imply that the alpha-GalA KO mouse is a good model in which to study the peripheral small fiber neuropathy exhibited by FD patients | 25337704 |
2014-12-20 12:00:00 | This study demonistrated that consistent neuropathological and neurodegenerative phenotype existing in the brains of aged alpha-Gal A-deficient mice. | 24529306 |
2014-03-08 10:48:00 | we demonstrate an age-dependent microvasculopathy of the mesenteric artery in a murine model of Fabry disease (galactosidase A-knockout mice) resulting from dysregulation of the vascular homeostatic enzyme endothelial nitric oxide synthase (eNOS) | 24232002 |
Type | IDs |
---|---|
Synonymous | Ags |
Gene |
UniProtKB-ID:
Q3UM38_MOUSE,
Q8BGZ6_MOUSE
UniprotKB:
Q3UM38,
Q8BGZ6
UniParc:
UPI00000EB994,
UPI00005AC3C4
EMBL:
AK040081,
BX004852,
AK054547,
AK145148,
AK164231
Ensembl:
ENSMUSG00000031266
KO:
mmu:11605
|
Nucleutide sequences |
EMBL-CDS:
BAE26260.1,
BAC35819.1,
BAC30508.1,
BAE37692.1
Ensembl_TRS:
ENSMUST00000239113
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000159121
RefSeq:
NP_038491.2
|
Others |
UniRef100:
UniRef100_P51569,
UniRef100_Q3UM38
UniRef90:
UniRef90_P51569
UniRef50:
UniRef50_P51569
UniGene:
Mm.1114
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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