| Type | Description |
|---|---|
| Definition | recombination activating 2 |
| Date | Results | Publications |
|---|---|---|
| 2021-02-13 13:22:00 | A Large Cohort of RAG1/2-Deficient SCID Patients-Clinical, Immunological, and Prognostic Analysis. | 31838659 |
| 2020-05-02 10:49:00 | Atypical Omenn Syndrome Due to RAG2 Gene Mutation. | 31885011 |
| 2020-02-29 10:09:00 | this study demonstrates recombination activity of human RAG2 mutations and correlation with clinical phenotype | 29772310 |
| 2019-11-16 13:41:00 | The RAG2 cleavage in developing T and B cells signals transcriptional activation of a genetic program that modulates cellular localization and includes genes important for proper lymphocyte selection. | 30782849 |
| 2018-11-17 11:23:00 | Estimated disease incidence of RAG1/2 mutations: A case report and querying the Exome Aggregation Consortium. | 27609655 |
| Type | IDs |
|---|---|
| Synonymous | RAG-2 |
| Gene |
UniProtKB-ID:
RAG2_HUMAN
UniprotKB:
P55895
UniParc:
UPI00001330E9
EMBL:
M94633,
AK292664,
BC022397,
CH471064
Ensembl:
ENSG00000175097
KO:
hsa:5897
|
| Nucleutide sequences |
EMBL-CDS:
EAW68117.1,
BAF85353.1,
AAH22397.1
Ensembl_TRS:
ENST00000311485,
ENST00000618712
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000308620,
ENSP00000478672
RefSeq:
NP_001230714.1,
NP_000527.2,
NP_001230715.1
|
| Others |
UniRef100:
UniRef100_P55895
UniRef90:
UniRef90_P55895
UniRef50:
UniRef50_P55895
UniGene:
Hs.714519
CCDS:
CCDS7903.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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