| HLA-A66 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| (MHC Class I, A cell surface antigen) | ||||||||||||||||
![]() HLA-A66  | ||||||||||||||||
| About | ||||||||||||||||
| Protein | transmembrane receptor/ligand | |||||||||||||||
| Structure | αβ heterodimer | |||||||||||||||
| Subunits | HLA-A*66--, β2-microglobulin | |||||||||||||||
| Older names | A10 | |||||||||||||||
| Subtypes | ||||||||||||||||
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| Rare alleles | ||||||||||||||||
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| Alleles link-out to IMGT/HLA database at EBI | ||||||||||||||||
HLA-A66 (A66) is a human leukocyte antigen serotype within HLA-A serotype group. The serotype is determined by the antibody recognition of α66 subset of HLA-A α-chains. For A66, the alpha "A" chain are encoded by the HLA-A*66 allele group and the β-chain are encoded by B2M locus.[1] A66 and A*66 are almost synonymous in meaning. A66 is a split antigen of the broad antigen serotype A10. A66 is a sister serotype of A25, A26, A34, and A43.
A66 is more common in Africa and Southwest Europe. A66 (A*6601) is believed to have been formed by a single gene conversion between another HLA-A and the A*2601 allele.[2].
Serotype
| A*66 | A66 | A10 | A26 | A34 | Sample | 
| allele | % | % | % | % | size (N) | 
| *6601 | 20 | 10 | 61 | 8 | 799 | 
| *6602 | 38 | 10 | 4 | 27 | 205 | 
| *6603 | 32 | 7 | 7 | 18 | 28 | 
A66 serotyping is poor. A*6601 is also sometimes recognized by A25, and A*6602 is often recognized by A74.
A*6601 Frequencies
| freq | ||
| ref. | Population | (%) | 
| [4] | Cameroon Sawa | 7.7 | 
| [4] | Kenya Luo | 6.8 | 
| [4] | Cameroon Sawa | 7.7 | 
| [4] | Cameroon Bakola Pygmy | 5.8 | 
| [4] | Cameroon Baka Pygmy | 5.0 | 
| [4] | Kenya Nandi | 5.0 | 
| [4] | Zimbabwe Harare Shona | 0.2 | 
| [4] | Cameroon Baka Pygmy | 5.0 | 
| [4] | Cameroon Beti | 4.6 | 
| [4] | Cameroon Bamileke | 4.5 | 
| [4] | India West Bhils | 4.0 | 
| [4] | Zimbabwe Harere Shona | 3.8 | 
| [4] | Uganda Kampala | 3.8 | 
| [4] | India Mumbai Marathas | 2.5 | 
| [4] | Cape Verde Northwestern | 2.5 | 
| [4] | Czech republic | 2.4 | 
| [4] | Morocco Nador Metalsa | 2.1 | 
| [4] | Central Portugal | 2.0 | 
| [4] | India West Parsis | 2.0 | 
| [4] | South African Natal Zulu | 2.0 | 
| [4] | Kenya | 1.7 | 
| [4] | Tunisia Tunis | 1.7 | 
| [4] | Guinea Bissau | 1.5 | 
| [4] | Georgia Tbilisi | 1.4 | 
| [4] | Zambia Lusaka | 1.2 | 
| [4] | Italy Bergamo | 1.1 | 
| [4] | Pakistan Karachi Parsi | 1.1 | 
| [4] | Oman | 0.8 | 
| [4] | Sudanese | 0.8 | 
| [4] | Belgium | 0.5 | 
| [4] | Southeast France | 0.4 | 
| [4] | Mongolia Buriat | 0.4 | 
| [4] | Wales | 0.2 | 
| freq | ||
| ref. | Population | (%) | 
| [4] | South African Natal Zulu | 1.5 | 
| [4] | Cameroon Yaounde | 1.1 | 
| [4] | Cameroon Bamileke | 0.6 | 
| [4] | Senegal Niokholo Mandenka | 0.5 | 
| [4] | Kenya Nandi | 0.4 | 
| [4] | Zimbabwe Harare Shona | 0.2 | 
| [4] | Wales | 0.03 | 
| HLA A*6603 frequencies | ||
| freq | ||
| ref. | Population | (%) | 
| [4] | Cameroon Pygmy Baka | 10.0 | 
| [4] | Cameroon Bakola Pygmy | 9.0 | 
| [4] | Cameroon Sawa | 7.7 | 
| [4] | CAR Mbenzele Pygmy | 2.8 | 
| [4] | Zimbabwe Harare Shona | 0.2 | 
References
- ↑ Arce-Gomez B, Jones EA, Barnstable CJ, Solomon E, Bodmer WF (February 1978). "The genetic control of HLA-A and B antigens in somatic cell hybrids: requirement for beta2 microglobulin". Tissue Antigens. 11 (2): 96–112. doi:10.1111/j.1399-0039.1978.tb01233.x. PMID 77067.
 - ↑ Madrigal JA, Hildebrand WH, Belich MP, et al. (1993). "Structural diversity in the HLA-A10 family of alleles: correlations with serology". Tissue Antigens. 41 (2): 72–80. doi:10.1111/j.1399-0039.1993.tb01982.x. PMID 8475492.
 - ↑ Allele Query Form IMGT/HLA - European Bioinformatics Institute
 - 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45  Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database: http://www.allelefrequencies.net". Tissue Antigens. 61 (5): 403–7. doi:10.1034/j.1399-0039.2003.00062.x. PMID 12753660. 
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