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Molecular screening for Vel- blood type and analysis of SMIM1 gene variants / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 1349-1351, 2020.
Article in Chinese | WPRIM | ID: wpr-879496
ABSTRACT
OBJECTIVE@#To screen for Vel- rare blood type donors and determine the frequency of SMIM1 c.64_80del allele in Yili Prefecture of Xinjiang, China.@*METHODS@#DNA pooling and PCR-sequence-specific primers (PCR-SSP) was conducted to screen individuals carrying the SMIM1 c.64_80del variant, and Sanger sequencing of SMIM1 exon 3 was carried out to verify the genotype of those with the variation. SMIM1 intron 2 was also sequenced to identify single nucleotide polymorphisms (SNPs) that may affect the expression of Vel antigen.@*RESULTS@#Among 3328 blood donors, 14 were identified as heterozygotes for the SMIM1 c.64_80del allele, its allele frequency was 0.21%; no homozygous SMIM1 c.64_80 deletions was found. For SNP rs1175550, all of the 14 individuals had an AA genotype, among whom 5 carried heterozygous 7111ins GCA variant in intron 2.@*CONCLUSION@#The allelic frequency of SMIM1 c.64_80del in Yili area is approximately 0.21%, which is reported for the first time.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Genetic Variation / Blood Group Antigens / China / Polymorphism, Single Nucleotide / Alleles / Gene Frequency / Genotype / Membrane Proteins Type of study: Diagnostic study / Screening study Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2020 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Genetic Variation / Blood Group Antigens / China / Polymorphism, Single Nucleotide / Alleles / Gene Frequency / Genotype / Membrane Proteins Type of study: Diagnostic study / Screening study Limits: Humans Country/Region as subject: Asia Language: Chinese Journal: Chinese Journal of Medical Genetics Year: 2020 Type: Article