| Type | Description |
|---|---|
| Definition | NIPA magnesium transporter 2 |
| Date | Results | Publications |
|---|---|---|
| 2020-07-11 12:57:00 | AGEs dose-dependently down-regulated the expression of NIPA2 in osteoblasts. NIPA2 also regulated osteoblast apoptosis by affecting the intracellular magnesium level and further affecting the osteogenic capacity of osteoblasts. | 31003774 |
| 2015-06-27 10:23:00 | This study primarily reveals that a selective magnesium transporter NIPA2 may play a role in the pathogenesis of CAE. | 25347071 |
| 2012-11-24 11:18:00 | mutations in NIPA2 gene were associated with childhood absence epilepsy (CAE), which indicated that the haploinsufficiency of NIPA2 might be a candidate mechanism underlying the IGE/CAE phenotypes caused by 15q11.2 microdeletions or rare mutations in NIPA2 | 22367439 |
| 2010-01-21 00:00:00 | located in the genomic domain between break points 1 and 2 on chromosome 15, of the Prader-Willi/Angelman syndromes | 14508708 |
| 2010-01-21 00:00:00 | quantitated mRNA levels of NIPA2, NIPA2,l CYFIP1, and GCP5 in Prader-Willi syndrome and correlated levels with psychological and behavior scales | 16982806 |
| Type | IDs |
|---|---|
| Synonymous | SLC57A2 |
| Gene |
UniProtKB-ID:
NIPA2_HUMAN,
A0A024R372_HUMAN
UniprotKB:
Q8N8Q9,
A0A024R372
UniParc:
UPI00004B247B,
UPI0000070013
EMBL:
CH471258,
AK096305,
BK001120,
CR606982,
BC011775,
AK300843,
BC000957,
AY732242,
AC011767
Ensembl:
ENSG00000140157
KO:
hsa:81614
|
| Nucleutide sequences |
EMBL-CDS:
AAH11775.1,
BAC04757.1,
AAH00957.3,
AAU34000.1,
BAG62494.1,
DAA01509.1,
EAW65552.1,
EAW65554.1,
EAW65553.1
Gene_ORFName:
hCG_1735857
Ensembl_TRS:
ENST00000359727,
ENST00000398013,
ENST00000674330,
ENST00000337451,
ENST00000674173,
ENST00000674289,
ENST00000398014,
ENST00000539711,
ENST00000674477
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000381096,
ENSP00000501373,
ENSP00000501408,
ENSP00000337618,
ENSP00000501412,
ENSP00000437746,
ENSP00000381095,
ENSP00000352762,
ENSP00000501489
RefSeq:
NP_001008892.1,
XP_016878148.1,
XP_016878138.1,
XP_011542182.1,
XP_016878143.1,
XP_005272605.1,
XP_016878141.1,
NP_001008860.1,
XP_016878146.1,
XP_006720427.1,
XP_005272610.1,
XP_016878150.1,
XP_016878147.1,
XP_005272603.1,
XP_005272607.1,
NP_001008894.1,
NP_001171817.1,
XP_016878151.1,
XP_011542181.1,
XP_016878136.1,
XP_016878144.1,
XP_006720429.1,
NP_001171818.1,
XP_016878152.1,
XP_016878142.1,
XP_016878139.1,
XP_011542179.1,
XP_016878134.1,
XP_006720430.1,
XP_005272604.1,
XP_016878137.1,
XP_011542180.1,
XP_016878145.1,
XP_016878140.1,
XP_024305851.1,
XP_006720428.1,
XP_016878149.1,
XP_016878135.1,
XP_005272609.1,
NP_112184.4
|
| Others |
UniRef100:
UniRef100_Q8N8Q9
UniRef90:
UniRef90_Q9JJC8
UniRef50:
UniRef50_Q9JJC8
UniGene:
Hs.591003
CCDS:
CCDS73693.1,
CCDS73694.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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