Type | Description |
---|---|
Definition | solute carrier family 41 member 1 |
Date | Results | Publications |
---|---|---|
2017-11-11 12:49:00 | Knockdown of SLC41A1 magnesium transporter promotes mineralization and attenuates magnesium inhibition during osteogenesis of mesenchymal stromal cells. | 28222767 |
2017-03-11 11:41:00 | The association of rs11240569 polymorphism in SLC41A1 gene with reduced risk of Parkinson's Disease was replicated in our population. | 27612022 |
2016-09-10 11:31:00 | Authors performed direct DNA sequencing of the SLC41A1 gene in 100 early-onset PD cases. | 26308152 |
2016-02-13 12:49:00 | Na+-dependent Mg2+ efflux conducted by Na+/Mg2+ exchanger SLC41A1 is regulated by insulin. | 26355001 |
2015-01-17 11:53:00 | This study has shown loss of Mg(2+) efflux function consequent to SLC41A1 R244H variant and SLC41A1 coding variants seem to be rare in Taiwanese Parkinson disease. | 24661466 |
Type | IDs |
---|---|
Synonymous | MgtE |
Gene |
UniProtKB-ID:
S41A1_HUMAN,
B2RMP2_HUMAN
UniprotKB:
Q8IVJ1,
B2RMP2
UniParc:
UPI000013E1E6
EMBL:
BX641054,
AJ514402,
AL832362,
BC136303,
AL831974,
BX648979,
CH471067,
AL832001,
AK128069
Ensembl:
ENSG00000133065
KO:
hsa:254428
|
Nucleutide sequences |
EMBL-CDS:
CAH56213.1,
CAH56217.1,
CAH56211.1,
CAE46028.1,
CAH56135.1,
CAD58404.1,
BAG54625.1,
AAI36304.1,
EAW91583.1,
EAW91582.1
Gene_ORFName:
hCG_19155
Ensembl_TRS:
ENST00000367137
|
Protein sequencees |
Ensembl_PRO:
ENSP00000356105
RefSeq:
NP_776253.3,
XP_005245126.1
|
Others |
UniRef100:
UniRef100_Q8IVJ1
UniRef90:
UniRef90_Q8IVJ1
UniRef50:
UniRef50_Q8IVJ1
UniGene:
Hs.20274
CCDS:
CCDS30988.1
|
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