HLA-A66

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major histocompatibility complex (human), class I, A66
Alleles A*6601
A*6602
A*6603
Structure (See HLA-A)
Identifiers
6601 6602 6603
Symbol(s) HLA-A
EBI-HLA A*6601
EBI-HLA A*6602
EBI-HLA A*6603
Shared data
Locus chr.6 6p21.31

HLA-A66 (A66) is an HLA-A serotype. The serotype identifies the more common HLA-A*66 gene products. A66 is a split antigen type of the A10 broad antigen type. A*6601 is believed to have been formed by a single gene conversion between another HLA-A and the A*2601 allele.[1] A66 is more common in Africa and SW Europe. A66 is uncommon.


Serotype

A66, A10 serotype recognition of Some HLA A*66 allele-group gene products[2]
A*66 A66 A10 A26 Other Sample
allele  %  %  %  % size (N)
6601 20 10 61 3 799
6602 38 10 4 31 205
6603 32 7 7 18 28





A*6601 Frequencies

HLA A*6601 frequencies
freq
ref. Population (%)
[3] Cameroon Sawa7.7
[3] Kenya Luo6.8
[3] Cameroon Sawa7.7
[3] Cameroon Bakola Pygmy5.8
[3] Cameroon Baka Pygmy5.0
[3] Kenya Nandi5.0
[3] Zimbabwe Harare Shona0.2
[3] Cameroon Baka Pygmy5.0
[3] Cameroon Beti4.6
[3] Cameroon Bamileke4.5
[3] India West Bhils4.0
[3] Zimbabwe Harere Shona3.8
[3] Uganda Kampala3.8
[3] India Mumbia Marathas2.5
[3] Cape Verde Northwestern 2.5
[3] Czech republic2.4
[3] Morocco Nador Metalsa2.1
[3] Central Portugal2.0
[3] India West Parsis2.0
[3] South Africian Natal Zulu2.0
[3] Kenya1.7
[3] Tunisia Tunis1.7
[3] Guinea Bissau1.5
[3] Georgia Tibilisi1.4
[3] Zambia Lusaka1.2
[3] Italy Bergamo1.1
[3] Pakistan Karachi Parsi1.1
[3] Oman0.8
[3] Sudanese0.8
[3] Belgium0.5
[3] Southeast France0.4
[3] Mongolia Buriat0.4
[3] Wales0.2
HLA A*6602 frequencies
freq
ref. Population (%)
[3] South Africian Natal Zulu1.5
[3] Cameroon Yaounde1.1
[3] Cameroon Bamileke0.6
[3] Senegal Niokholo Mandenka0.5
[3] Kenya Nandi0.4
[3] Zimbabwe Harare Shona0.2
[3] Wales0.03
HLA A*6603 frequencies
freq
ref. Population (%)
[3] Cameroon Pygmy Baka10.0
[3] Cameroon Bakola Pygmy9.0
[3] Cameroon Sawa7.7
[3] CAR Mbenzele Pygmy2.8
[3] Zimbabwe Harare Shona0.2


References

  1. 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. PMID 8475492.
  2. derived from IMGT/HLA
  3. 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 3.12 3.13 3.14 3.15 3.16 3.17 3.18 3.19 3.20 3.21 3.22 3.23 3.24 3.25 3.26 3.27 3.28 3.29 3.30 3.31 3.32 3.33 3.34 3.35 3.36 3.37 3.38 3.39 3.40 3.41 3.42 3.43 3.44 Middleton D, Menchaca L, Rood H, Komerofsky R (2003). "New allele frequency database: http://www.allelefrequencies.net". Tissue Antigens 61 (5): 403-7. PMID 12753660.
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Acknowledgement and Attribution Regarding Sources of Content

Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

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