Phenotype: CD8 deficiency, familial


OMIM: 608957
Inheritance: Autosomal recessive
Classification: Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

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CD8A || c.331G>A

Gene/Locus:    CD8A
Dna Change:    c.331G>A
Protein Change:    p.Gly111Ser
Mutation Type:    Substitution
Mutation Effect:    Missense
Location:    exon 2
Transcript:    NM_001768.6

PopulationEthnic GroupRegionMutation FrquencyCoalescence TimeReference
SpainGypsyNAcarrier rate of 0.4%NAMancebo E et al., 2008Mancebo E, Moreno-Pelayo MA, Mencía A, de la Calle-Martín O, Allende LM, Sivadorai P, Kalaydjieva L, Bertranpetit J, Coto E, Calleja-Antolín S, Ruiz-Contreras J, Paz-Artal E, . Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.. Mol. Immunol.. 2008; 45(2):479-84

References

Mancebo E, Moreno-Pelayo MA, Mencía A, de la Calle-Martín O, Allende LM, Sivadorai P, Kalaydjieva L, Bertranpetit J, Coto E, Calleja-Antolín S, Ruiz-Contreras J, Paz-Artal E, Gly111Ser mutation in CD8A gene causing CD8 immunodeficiency is found in Spanish Gypsies.Mol. Immunol.. 2008; 45(2):479-84