NFKBIA
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 14[15]
- Cytogenetic location
- 14q13.2[19]
- Encodes
- NFKB inhibitor alpha, NF-kappa-B inhibitor alpha[12][13]
- Expressed in
- vena cava, pericardium, lower lobe of lung, oocyte, nipple, saphenous vein, mucosa of urinary bladder, beta cell, monocyte, upper lobe of lung[20][21][22][23][24][25][26][27][28][29]
- Found in taxon
- Homo sapiens[14]
- Genetic association
- ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant, Hypohidrotic ectodermal dysplasia with immune deficiency[16][17]
- HomoloGene ID
- 7863[3]
- Strand orientation
- reverse strand[18]
🏷️ Also known as
en EDAID2
en IKBA
en MAD-3
en NFKBI
en NFKBIA
en NFKB inhibitor alpha
🔖 Identifiers · 13
- OpenAlex ID
- C2779730028
- Image (Wikimedia Commons)
- 1NFI.png ↗
- Ensembl gene ID
- ENSG00000100906
- Ensembl transcript ID
- ENST00000557459, ENST00000216797, ENST00000553342, ENST00000554001, ENST00000555371, ENST00000555629, ENST00000556664, ENST00000557100, ENST00000557140, ENST00000557389
- Entrez Gene ID
- 4792
- Exact match
- identifiers.org
- Freebase ID
- /m/03c97s5
- HGNC ID
- 7797
- HGNC gene symbol
- NFKBIA
- Microsoft Academic ID (discontinued)
- 2779730028
- OMIM ID
- 164008
- RefSeq RNA ID
- NM_020529
Show all 13 identifiers +1
- UMLS CUI
- C1334877
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Summary
NFKBIA is a gene[1].