| Type | Description |
|---|---|
| Definition | glutamate ionotropic receptor NMDA type subunit 3B |
| Date | Results | Publications |
|---|---|---|
| 2017-03-18 13:19:00 | GRIN3B missense mutation is an inherited risk factor for schizophrenia. | 28132660 |
| 2016-03-19 11:35:00 | Authors investigated the significance of a common human genetic variation of the NMDAR NR3B subunit | 25768306 |
| 2014-12-20 10:45:00 | Rs2240158 of GRIN3B was significantly associated with mismatch negativity in healthy subjects. | 24814139 |
| 2010-06-30 22:07:00 | Observational study of gene-disease association. (HuGE Navigator) | 20398908 |
| 2010-06-28 12:08:00 | our findings suggest that the over-expression of NR3B subunit of NMDA receptor is a long lasting result of chronic opioid abuse. | 20153313 |
| Type | IDs |
|---|---|
| Synonymous | GluN3B, NR3B |
| Gene |
UniProtKB-ID:
NMD3B_HUMAN,
Q5F0I5_HUMAN
UniprotKB:
O60391,
Q5F0I5
UniParc:
UPI000004064B,
UPI00004CCEDC
EMBL:
AY507106,
BK004079,
BK000070,
AC004528
Ensembl:
ENSG00000116032
KO:
hsa:116444
|
| Nucleutide sequences |
EMBL-CDS:
DAA04570.1,
AAC12680.1,
DAA00018.1,
AAS87020.1
Ensembl_TRS:
ENST00000234389
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000234389
RefSeq:
XP_016881732.1,
NP_619635.1
|
| Others |
UniRef100:
UniRef100_Q5F0I5,
UniRef100_O60391
UniRef90:
UniRef90_O60391
UniRef50:
UniRef50_O60391
UniGene:
Hs.660378
CCDS:
CCDS32861.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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