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Blood group gene RHD variation
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创建时间：
2021-10-15
相关数据集
BGMUT
BGMUT documents variations in genes that encode antigens for human blood groups.
国家生物信息中心2025-10-11 更新620
First observation of a mutation (R192Q) in a weak KEL2 phenotype encoded by 575 G>A, ethnic origin: Austria.. Homo sapiens KEL gene for Kell blood group system, KEL(R192Q) allele, exons 1-19.
Standard serologic typing identified a weakened KEL:2 expression in a blood donor sample. Molecular characterization identified a c.575G>A change on a KEL*2 background.
NIAID Data Ecosystem90
Data from: Haplotype sequence collection of ABO blood group alleles by long-read sequencing reveals putative A1-diagnostic variants
In the era of blood group genomics, reference collections of complete and fully-resolved blood group gene alleles have gained high importance. For most blood groups, however, such collections are cu
DataCite Commons2025-04-01 更新70
Additional file 1: Table S1. of ABO allele-level frequency estimation based on population-scale genotyping by next generation sequencing
Primer sequences for ABO assay 1 and 2. Table S2. Alleles excluded from the reference allele set downloaded from NCBI dbRBC. Table S3. Alleles included in our final reference allele set and definition
NIAID Data Ecosystem90
ABO phenotype protected reproduction as it is based on fucosylations.
The molecular biological relationship between human fertility and ABO(H) blood group phenotype formation becomes evident with the rare (Oh) or Bombay blood type, which based on the history of h
DataCite Commons2020-09-04 更新80
