HLA-A25

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major histocompatibility complex (human), class I, A25
Alleles A*2501
A*2502
Structure (See HLA-A)
Identifiers
2501 2502
Symbol(s) HLA-A
EBI-HLA A*2501
EBI-HLA A*2502
Shared data
Locus chr.6 6p21.31

HLA-A25 (A25) is an HLA-A serotype. The serotype identifies the more common HLA-A*25 gene products. A25 is a split antigen of the A10 broad antigen serotype group. It is believed to have been formed by a single gene conversion between another HLA-A and the A*2601 allele.[1] A26 is more common in Western Europe.


Serotype

A25 and A10 serotype recognition of HLA A*2501 allele-group gene products[2]
A*25 A25 A10 Sample
allele  %  % size (N)
2501 95 2 1375
2502 80 5

There are 7 alleles for A25, 6 that result in different isoforms.

A25 frequencies

HLA A*2501 frequencies
freq
ref. Population (%)
[3] Saudi Arabia5.7
[3] India Jalpaiguri Toto5.2
[3] Russia Northwest5.0
[3] Spain Pas Valley4.3
[3] Czech Republic4.2
[3] Spain North Cantabrian4.2
[3] Russia Arkhangelsk Pomors4.0
[3] Croatia 3.9
[3] Spain North Cabuernigo3.8
[3] Russia Chuvash3.7
[3] Romanian3.5
[3] Italy Bergamo3.2
[3] Croatia 3.0
[3] Israel Ashkenazi Jews 2.8
[3] Bulgaria 2.7
[3] Spain Basque Arratia Valley 2.7
[3] Sweden Uppsala County 2.6
[3] Ireland Northern2.1
[3] Turkey 2.1
[3] Wales2.1
[3] Spain Eastern Andalusia 2.0
[3] Georgia Svaneti Svans1.9
[3] Italy1.9
[3] England Manchester1.9
[3] England Lancaster1.8
[3] Jews (Israel)1.7
[3] Macedonia1.7
[3] England Sheffield1.6
[3] Portugal South pop21.4
[3] Italy South Campania1.2
[3] Uganda Kampala1.2
[3] Finland1.1
[3] Portugal North1.1
[3] Belgium 1.0
[3] France Corsica1.0
[3] Mongolia Oold1.0
[3] Russia Murmansk Saomi1.0
[3] Tunisia 1.0
[3] France South East0.8
[3] Morocco Nador Metalsa0.7
[3] Greece 0.6
[3] Italy North Pavia0.6
[3] Algeria0.5
[3] China Qinghai Hui0.5
[3] Guatemala Mayans0.4
[3] Russia Nenets0.4
[3] Cameroon Beti0.3
[3] Beijing Shijiazhuang0.1
[3] Taiwan Hakka0.1

A*2501 distribution is primarily located in western Eurasia. Frequency tends to be highest in the populations that underwent later neolithization suggesting A*2501 spread in Europe. The high frequency in Saudi Arabia is suggestive of a source.

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 3.45 3.46 3.47 3.48 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 .