|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Disruption of the RAG2 zinc finger motif impairs protein stability and causes immunodeficiency.
|
26692406 |
2016 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disorders.
|
25516070 |
2015 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Leaky RAG Deficiency in Adult Patients with Impaired Antibody Production against Bacterial Polysaccharide Antigens.
|
26186701 |
2015 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Crystal structure of the V(D)J recombinase RAG1-RAG2.
|
25707801 |
2015 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Crystal structure of the V(D)J recombinase RAG1-RAG2.
|
25707801 |
2015 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
|
24290284 |
2014 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
|
24290284 |
2014 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Analysis of mutations and recombination activity in RAG-deficient patients.
|
21131235 |
2011 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Hypomorphic Rag mutations can cause destructive midline granulomatous disease.
|
20489056 |
2010 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency.
|
18822103 |
2009 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.
|
19458910 |
2009 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A novel missense RAG-1 mutation results in T-B-NK+ SCID in Athabascan-speaking Dine Indians from the Canadian Northwest Territories.
|
18701881 |
2009 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCID.
|
19458910 |
2009 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
A novel missense RAG-1 mutation results in T-B-NK+ SCID in Athabascan-speaking Dine Indians from the Canadian Northwest Territories.
|
18701881 |
2009 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Saving the red baby: successful allogeneic cord blood transplantation in Omenn syndrome.
|
19064334 |
2009 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report.
|
19830075 |
2009 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GermlineCausalMutation
|
disease |
ORPHANET |
An immunodeficiency disease with RAG mutations and granulomas.
|
18463379 |
2008 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
GermlineCausalMutation
|
disease |
ORPHANET |
An immunodeficiency disease with RAG mutations and granulomas.
|
18463379 |
2008 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
An immunodeficiency disease with RAG mutations and granulomas.
|
18463379 |
2008 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical application of DNA microarrays: molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency.
|
18442948 |
2008 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
An immunodeficiency disease with RAG mutations and granulomas.
|
18463379 |
2008 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Clinical application of DNA microarrays: molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency.
|
18442948 |
2008 |
|
| Entrez Id: |
5897 |
| Gene Symbol: |
RAG2 |
RAG2
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
RAG2 PHD finger couples histone H3 lysine 4 trimethylation with V(D)J recombination.
|
18033247 |
2007 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Biochemical and folding defects in a RAG1 variant associated with Omenn syndrome.
|
18056378 |
2007 |
|
| Entrez Id: |
5896 |
| Gene Symbol: |
RAG1 |
RAG1
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes.
|
17572155 |
2007 |