major histocompatibility complex (human), class I, B47 | ||
Alleles | B*4701 B*4702 B*4703 | |
Structure (See HLA-B) | ||
Symbol(s) | HLA-B | |
EBI-HLA | B*4701 | |
EBI-HLA | B*4702 | |
EBI-HLA | B*4703 | |
Locus | chr.6 6p21.31 |
HLA-B47 (B47) is an HLA–B serotype. The serotype identifies the HLA-B*47 gene products (B*4701, B*4702, B*4703) . Comparison of B47 nucleotide sequence with other HLA-B sequences shows a segment of 228 bp identical with B44 in the alpha 1 domain and a segment of 218 bp identical with B27 in the alpha 2 domain, but only a 91 bp segment of identity with B13 in the alpha 1 domain. The complex pattern of substitutions and their degree of divergence indicate that HLA-B13 and HLA-Bw47 alleles are not related by a simple mutational event. B47 is linked to (close to on the chromosome) a gene that causes adrenal deficiency. B47 is generally low in frequency and with highest known frequencies in Central and Western Africa. (For terminology help see: HLA-serotype tutorial)
Serotype
B*47 | B47 | Other | Sample |
allele | % | % | size (N) |
4701 | 50 | 37 | 317 |
4702 | 40 | 40 | 5 |
4703 | 25 | 50 | 4 |
Serotyping for B47 is poor and typing is best performed with SSP-PCR or gene sequencing.
Disease Associations
B47 is linked to Adrenal 21-hydroxylase deficiency. The CYP21 gene is located close to B47 between HLA-B and HLA-DRB1 locus.
B*4701 frequencies
freq | ||
ref. | Population | (%) |
Bamileke (Cameroon) | 2.6 | |
Zapotec (Oaxaca, Mexico) | 2.2 | |
Niokholo Mandinka (Senegal) | 1.6 | |
Mbenzele Pygmy (CAR) | 1.5 | |
Nandi (Kenya) | 1.3 | |
Sudanese | 1.3 | |
Yaoundé City (Cameroon) | 1.1 | |
Lusaka (Zambia) | 1.1 | |
Central Portugal | 1.0 | |
Bulgaria | 0.9 | |
Czech Republic | 0.9 | |
Cape Verde Islands | 0.8 | |
Berber (Morocco) | 0.7 | |
Finland | 0.6 | |
Svans (Georgia) | 0.6 | |
Bergamo (Italy) | 0.6 | |
Romanians | 0.6 | |
North Delhi ((India)) | 0.5 | |
Orkney Isles (Scotland) | 0.5 | |
Basque (Gipuzkoa, Spain) | 0.5 | |
Southeastern (France) | 0.4 | |
Oman | 0.4 | |
Kenya | 0.3 |
References
- Marsh, S. G.; Albert, E. D.; Bodmer, W. F.; Bontrop, R. E.; Dupont, B.; Erlich, H. A.; Fernández-Viña, M.; Geraghty, D. E.; Holdsworth, R.; Hurley, C. K.; Lau, M.; Lee, K. W.; Mach, B.; Maiers, M.; Mayr, W. R.; Müller, C. R.; Parham, P.; Petersdorf, E. W.; Sasazuki, T.; Strominger, J. L.; Svejgaard, A.; Terasaki, P. I.; Tiercy, J. M.; Trowsdale, J. (2010). "Nomenclature for factors of the HLA system, 2010". Tissue Antigens. 75 (4): 291–455. doi:10.1111/j.1399-0039.2010.01466.x. PMC 2848993. PMID 20356336.
- ^ Zemmour J, Ennis PD, Parham P, Dupont B (1988). "Comparison of the structure of HLA-B47 to HLA-B13 and its relationship to 21-hydroxylase deficiency". Immunogenetics. 27 (4): 281–7. doi:10.1007/BF00376123. PMID 3257938.
- derived from IMGT/HLA
- ^ Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database". Tissue Antigens. 61 (5): 403–7. doi:10.1034/j.1399-0039.2003.00062.x. PMID 12753660.
HLA-B serotypes and allele groups | |
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