RAG2

GENERAL INFORMATION

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Gene name

RAG2

Gene description

Recombination activating gene 2

Protein class

Disease related genes
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

5
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enriched (thyroid gland)
GTEx:Tissue enriched (thyroid gland)

Protein evidence

Evidence at protein level

ANTIBODY RELIABILITY

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Data reliability

Pending normal tissue annotation.
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
N/A
Endocrine tissues
N/A
Bone marrow & immune system
N/A
Muscle tissues
N/A
Lung
N/A
Nasopharynx
N/A
N/A
Bronchus
N/A
N/A
Lung
N/A
Liver & gallbladder
N/A
Liver
N/A
Pancreas
N/A
Pancreas
N/A
Gastrointestinal tract
N/A
Kidney & urinary bladder
N/A
Male tissues
N/A
Testis
N/A
Epididymis
N/A
N/A
Prostate
N/A
Seminal vesicle
N/A
N/A
Female tissues
N/A
Breast
N/A
N/A
Vagina
N/A
N/A
Cervix, uterine
N/A
N/A
Ovary
N/A
Placenta
N/A
Adipose & soft tissue
N/A
Skin
N/A
Skin
N/A


PROTEIN EXPRESSION OVERVIEW

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Pending normal tissue annotation.


RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enriched (thyroid gland)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enriched (thyroid gland)

Organ

Expression



GENE INFORMATION

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Gene name

RAG2

Synonyms

Description

Recombination activating gene 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a protein that is involved in the initiation of V(D)J recombination during B and T cell development. This protein forms a complex with the product of the adjacent recombination activating gene 1, and this complex can form double-strand breaks by cleaving DNA at conserved recombination signal sequences. The recombination activating gene 1 component is thought to contain most of the catalytic activity, while the N-terminal of the recombination activating gene 2 component is thought to form a six-bladed propeller in the active core that serves as a binding scaffold for the tight association of the complex with DNA. A C-terminal plant homeodomain finger-like motif in this protein is necessary for interactions with chromatin components, specifically with histone H3 that is trimethylated at lysine 4. Mutations in this gene cause Omenn syndrome, a form of severe combined immunodeficiency associated with autoimmune-like symptoms. [provided by RefSeq, Jul 2008]

Chromosome

11

Cytoband

p12

Chromosome location (bp)

36575574 - 36598279

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000175097 (version 78.38)

Entrez gene

5897

UniProt

P55895 (UniProt - Evidence at protein level)

neXtProt

NX_P55895

Antibodypedia

RAG2 antibodies


PROTEIN BROWSER

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ENST00000311485
 
ENST00000527033
 
ENST00000529083
 
ENST00000532616
 
ENST00000618712
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

RAG2-001 ENSP00000308620
ENST00000311485
P55895
Show all »
Show » Show » 527 59.2 No 0
RAG2-003 ENSP00000436895
ENST00000527033
E9PQB9
Show all »
Show » Show » 71 8 No 0
RAG2-004 ENSP00000432174
ENST00000532616
Show » 1 0.1 No 0
RAG2-008 ENSP00000436327
ENST00000529083
E9PPU5
Show all »
Show » Show » 150 17 No 0
RAG2-201 ENSP00000478672
ENST00000618712
P55895
Show all »
Show » Show » 527 59.2 No 0