HLA-A32
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| major histocompatibility complex (human), class I, A32
| ||
| Alleles | A*3201 A*3202 A*3204 | |
| Structure (See HLA-A) | ||
| Identifiers | 3201 3202 3204
| |
| Symbol(s) | HLA-A | |
| EBI-HLA | A*3201 | |
| EBI-HLA | A*3202 | |
| EBI-HLA | A*3204 | |
| Locus | chr.6 6p21.31 | |
HLA-A32 (A32) is an HLA-A serotype. The serotype identifies the more common HLA-A*32 gene products. A32 is a split antigen of the A19 serotype group. This group also includes A29, A30, A31, A33, and A74 serotypes
Serotype
| A*32 | A32 | A19 | Sample |
| allele | % | % | size (N) |
| A3201 | 94 | 3441 | |
| A3202 | 67 | 3 | |
| A3201 | 17 | 17 | 6 |
Serotyping efficiency for the predominant allele is good. There are 16 known alleles that result in 15 isoforms of HLA-A32. One isoform may be poorly expressed.[2]
HLA-A*3201 allele frequencies
| freq | ||
| ref. | Population | (%) |
| [3] | Oman | 11.4 |
| [3] | Pakistan Brahui | 9.2 |
| [3] | Italy Sardinia (3) | 8.7 |
| [3] | Bulgaria | 8.2 |
| [3] | Burkina Faso Fulani | 8.2 |
| [3] | Pakistan Karachi Parsi | 7.8 |
| [3] | Pakistan Kalash | 7.5 |
| [3] | France South East | 7.2 |
| [3] | Pakistan Baloch | 7.1 |
| [3] | Georgia Tibilisi Kurds | 6.7 |
| [3] | Iran Baloch | 6.7 |
| [3] | Italy Bergamo | 5.9 |
| [3] | India North Hindus | 5.8 |
| [3] | Croatia | 5.7 |
| [3] | France Corsica | 5.5 |
| [3] | Sudanese | 5.5 |
| [3] | Pakistan Pathan | 5.1 |
| [3] | Pakistan Sindhi | 5.1 |
| [3] | Romanian | 5.0 |
| [3] | Cape Verde NW Islands | 4.8 |
| [3] | Georgia Tibilisi Georgians | 4.8 |
| [3] | Bulgaria Gipsy | 4.2 |
| [3] | Cape Verde SE Islands | 4.0 |
| [3] | Israel Arab Druse | 4.0 |
| [3] | Portugal Centre | 4.0 |
| [3] | Spain Majorca and Minorca | 3.9 |
| [3] | Burkina Faso Mossi | 3.8 |
| [3] | Guinea Bissau | 3.8 |
| [3] | Belgium | 3.7 |
| [3] | Cuban Mulatto | 3.6 |
| [3] | Cuban White | 3.6 |
| [3] | Australia New South Wales | 3.4 |
| [3] | Morocco Nador Metalsa | 3.4 |
| [3] | Ireland Northern | 3.2 |
| [3] | Jordan Amman | 3.1 |
| [3] | Portugal South | 3.1 |
| [3] | India Khandesh Pawra | 3.0 |
| [3] | India New Delhi | 3.0 |
| [3] | India West Coast Parsis | 3.0 |
| [3] | Azores Central Islands | 2.7 |
| [3] | India North Delhi | 2.7 |
| [3] | Pakistan Burusho | 2.7 |
| [3] | Kenya Luo | 2.6 |
| [3] | Spain Eastern Andalusia Gipsy | 2.6 |
| [3] | South Africian Natal Zulu | 2.5 |
| [3] | China North Han | 2.4 |
| [3] | Czech Republic | 2.4 |
| [3] | Mexico Mestizos | 2.4 |
| [3] | China Beijing | 2.2 |
| [3] | Finland | 2.2 |
| [3] | Uganda Kampala | 2.2 |
| [3] | Russia Tuva pop 2 | 2.1 |
| [3] | Brazil | 2.0 |
| [3] | Cameroon Beti | 2.0 |
| [3] | Cape Yk P. (Indig. Aust.) | 1.9 |
| [3] | Italy North pop 1 | 1.9 |
| [3] | Kenya Nandi | 1.9 |
| [3] | Tunisia | 1.5 |
| [3] | Georgia Svaneti Svans | 1.3 |
| [3] | New Caledonia | 1.2 |
| [3] | Golla (Andhra Prad. India) | 1.1 |
| [3] | Senegal Niokholo Mandenka | 1.1 |
| [3] | Thailand | 1.1 |
| [3] | Cameroon Bakola Pygmy | 1.0 |
| [3] | China Inner Mongolia | 1.0 |
| [3] | Kenya | 1.0 |
| [3] | Javanese (Singapore) | 1.0 |
| [3] | South Africa Natal Tamil | 1.0 |
| [3] | Basque (Gipuzkoa, Spain) | 1.0 |
| [3] | China Qinghai Hui | 0.9 |
| [3] | Tibet (china) | 0.9 |
| [3] | Zimbabwe Harare Shona | 0.9 |
| [3] | Beijing Shijiazhuang Tianjian | 0.8 |
| [3] | Groote Eylandt (Indig. Austr.) | 0.7 |
| [3] | Mali Bandiagara | 0.7 |
| [3] | Singapore Chinese | 0.7 |
| [3] | Argentina Toba Rosario | 0.6 |
| [3] | India Mumbai Marathas | 0.6 |
| [3] | Spain Catalonia Girona | 0.6 |
| [3] | Hong Kong Chinese | 0.4 |
| [3] | Yuendumu (indig. Australia) | 0.3 |
| [3] | Thailand Northeast | 0.2 |
A32 is most common around the Persion Gulf and the Mediterranean Basin. It has a consistent presence in Europe. The A32 frequenceies in the more isolated (genetically) peoples of Europe suggests that the A32 rise in the mediterranean may only be partially attributable to recent migrations from the middle eastern region. There is a node in southern europe around the Ionian Sea in which specific, European, A32-haplotypes are elevated.
A32 Haplotypes
| freq | ||
| ref. | Population | (%) |
| A32-B7(A*3201:B*0702) | ||
| Albanian | 2.2 | |
| Cuban | 1.9 | |
| [4] | Natal Zulu (S. Africa) | 1.0 |
| Cretan | 0.7 | |
| Cretan | 0.2 | |
| A32-B8(A*3201:B*0801) | ||
| N. Portugal | 2.2 | |
| Oman | 1.8 | |
| A32-B14(A*3201:B*14) | ||
| !kung | 1.9 | |
| Tunis | 1.8 | |
| Natal Zulu (S. Africa) | 1.0 | |
| Portugal | 1.1 | |
| Irish | 0.7 | |
| Italian | 0.6 | |
| A32-B27(A*3201:B27) | ||
| Gypsy(Spanish) | 6.0 | |
| E Black Sea (Turkey) | 2.3 | |
| German | 0.3 | |
| A32-B35 (A*3201:C*0401:B*3501) | ||
| Greek | 3.5 | |
| UA Emirates | 2.8 | |
| Sardinian | 2.6 | |
| Brahui (Pakistan) | 2.5 | |
| Tunisia | 1.8 | |
| Armenian | 1.7 | |
| Italian | 1.5 | |
| Oman | 1.3 | |
| Portugal | 1.1 | |
| German | 0.3 | |
| A32-B61(40) (A*3201:B*40) | ||
| Tunis | 1.2 | |
| Greek | 1.2 | |
| French | 0.6 | |
| German | 0.4 | |
| A32-B44 (A*3201:B*4402) | ||
| Austrian | 2.4 | |
| Belgium | 2.0 | |
| Albanian | 1.8 | |
| S. Portugal | 1.0 | |
| Irish | 0.7 | |
| German | 0.6 | |
| Dutch | 0.6 | |
| Senegal | 0.5 | |
| Italian | 0.4 | |
| A32-B51(A*3201:C*1201:B*5101) | ||
| Bulgarian | 1.8 | |
| German | 0.3 | |
| (A*3201:C*1502:B*5101) | ||
| Oman | 5.0 | |
| Baloch (Pakistan) | 3.2 | |
| Kalash | 2.9 | |
| UA Emirates | 1.9 | |
| Baloch (Iran) | 1.1 | |
| (A*3201:C*1401:B*5101) | ||
| Parsis (Karachi) | 4.9 | |
| Kalash | 2.9 | |
A common A32 haplotype A*3201-B*5101 can be found in Oman, United Arab Emirates, SE Iran, Bulgaria, and Portugal. A second, A*3201-B*3501 can be in the Omani, UAE, and Portugal.
References
- ↑ derived from IMGT/HLA
- ↑ Tang TF, Hou L, Tu B, et al (2006). "Identification of nine new HLA class I alleles in volunteers from the Singapore stem cell donor registries". Tissue Antigens 68 (6): 518–20. doi:10.1111/j.1399-0039.2006.00707.x. PMID 17176443.
- ↑ 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 3.45 3.46 3.47 3.48 3.49 3.50 3.51 3.52 3.53 3.54 3.55 3.56 3.57 3.58 3.59 3.60 3.61 3.62 3.63 3.64 3.65 3.66 3.67 3.68 3.69 3.70 3.71 3.72 3.73 3.74 3.75 3.76 3.77 3.78 3.79 3.80 3.81 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.
- ↑ B*0705
HLA-A Serotypes |
|---|
| HLA-A - A1 - A2 - A3 - A9 (A23 - A24) - A10 (A25 - A26 - A34 - A43 - A66) - A11 - A19 (A29 - A30 - A31 - A32 - A33 - A74) - A28 (A68 - A69) - A36 - A80 |
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 .

