CARD11
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 7[11]
- Cytogenetic location
- 7p22.2[15]
- Expressed in
- granulocyte, lymph node, spleen, appendix, blood, superficial temporal artery, parotid gland, palpebral conjunctiva, amniotic fluid, gallbladder[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- BENTA disease, severe combined immunodeficiency due to CARD11 deficiency[12][13]
- HomoloGene ID
- 13024[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en BENTA
en BIMP3
en CARD11
en CARMA1
en caspase recruitment domain family member 11
en IMD11
en IMD11A
en PPBL
🔖 Identifiers · 12
- CIViC gene ID
- 16180
- Ensembl gene ID
- ENSG00000198286
- Ensembl transcript ID
- ENST00000480332, ENST00000355508, ENST00000356408, ENST00000396946
- Entrez Gene ID
- 84433
- Exact match
- identifiers.org
- Freebase ID
- /m/03gxqqz
- HGNC ID
- 16393
- HGNC gene symbol
- CARD11
- Microsoft Academic ID (discontinued)
- 2781270172
- OMIM ID
- 607210
- RefSeq RNA ID
- NM_032415, NM_001324281
- UMLS CUI
- C1424244
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