| Type | Description |
|---|---|
| Definition | interferon gamma receptor 2 |
| Date | Results | Publications |
|---|---|---|
| 2019-11-16 11:46:00 | A purely quantitative form of partial recessive IFN-gammaR2 deficiency caused by mutations of the initiation or second codon. | 31222290 |
| 2019-04-19 09:36:00 | Successful unrelated cord blood transplant for complete IFN-gamma receptor 2 deficiency. | 27522156 |
| 2019-03-02 10:50:00 | A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations | 29106381 |
| 2018-09-15 10:06:00 | The study identified an SNP rs9978223 on IFNGR2 gene, associated with increased risk in acute myocardial infarctionpatient from India. | 29434065 |
| 2017-10-28 12:13:00 | A crystal structure of the extracellular part of human interferon-gamma receptor 2 (IFNGR2) was solved by molecular replacement at 1.8 A resolution. | 27599734 |
| Type | IDs |
|---|---|
| Synonymous | AF-1, IFGR2, IFNGT1, IMD28 |
| Gene |
UniProtKB-ID:
INGR2_HUMAN,
A8K881_HUMAN,
E7EUY1_HUMAN
UniprotKB:
P38484,
A8K881,
E7EUY1
UniParc:
UPI00001514B0,
UPI000066D9B7
EMBL:
KF510547,
AK292246,
U05877,
AP000300,
AY644470,
CH471079,
U05875,
AP000301,
AK314005,
KF457222,
BC003624,
U68755,
AP000302,
AP000299
Ensembl:
ENSG00000262795,
ENSG00000159128
KO:
hsa:3460
|
| Nucleutide sequences |
EMBL-CDS:
AAC52066.1,
AAA16955.1,
AAA16956.1,
AAT45458.1,
AAH03624.1,
BAG36717.1,
EAX09834.1,
BAF84935.1
Gene_ORFName:
hCG_401179
Ensembl_TRS:
ENST00000290219,
ENST00000576463,
ENST00000381995
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000458487,
ENSP00000290219,
ENSP00000371425
RefSeq:
NP_005525.2,
NP_001316057.1
|
| Others |
UniRef100:
UniRef100_E7EUY1,
UniRef100_P38484
UniRef90:
UniRef90_P38484
UniRef50:
UniRef50_P38484
UniGene:
Hs.634632
CCDS:
CCDS33544.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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