RAG1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 11[11]
- Cytogenetic location
- 11p12[18]
- Expressed in
- thymus, buccal mucosa cell, testicle, bone marrow, spleen, apex of heart, tendon of biceps brachii, stromal cell of endometrium, bone marrow cell, right adrenal cortex[19][20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive, Omenn syndrome, recombinase activating gene 1 deficiency, combined immunodeficiency with skin granulomas, combined immunodeficiency due to partial RAG1 deficiency[12][13][14][15][16]
- HomoloGene ID
- 387[3]
- Strand orientation
- forward strand[17]
🏷️ Also known as
en RAG-1
en RAG1
en recombination activating 1
en recombination activating gene 1
en RNF74
ar RAG١
🔖 Identifiers · 12
- Ensembl gene ID
- ENSG00000166349
- Ensembl transcript ID
- ENST00000534663, ENST00000299440, ENST00000529126
- Entrez Gene ID
- 5896
- Exact match
- identifiers.org
- Freebase ID
- /m/0w7lln2
- HGNC ID
- 9831
- HGNC gene symbol
- RAG1
- MeSH descriptor ID
- D016654
- MeSH tree code
- G05.360.340.024.340.400
- OMIM ID
- 179615
- RefSeq RNA ID
- NM_000448, XM_005253041, XM_011520250
- UMLS CUI
- C0085218
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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Summary
RAG1 is a gene[1].