BGMUT
BGMUT catalogs allelic variations in genes encoding human blood group antigens, documenting 1251 alleles across 40 gene loci affecting 30 human blood group systems.
Key Features:
- Comprehensive Allelic Data: Curated entries include detailed information on allelic variations collected from scientific literature and direct submissions by research laboratories.
- Geographic and Ethnic Prevalence Information: When available, reports provide geographic and ethnic distribution data for specific alleles.
- Integration with dbRBC Resource: BGMUT is integrated into the NCBI dbRBC resource for red blood cell biology.
Scientific Applications:
- Transfusion Medicine: Provides allele-level information relevant to blood compatibility assessment and antigen typing.
- Population Genetics and Human Evolution: Supports analyses of allele frequencies, human migrations, and evolutionary relationships among populations.
- Genetic Variation Research: Supplies locus-specific mutation data for studies of gene-specific variation in blood group antigen genes.
Methodology:
Content is manually curated from peer-reviewed publications and direct contributions from research laboratories.
Topics
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- SQL
- Added:
- 3/30/2017
- Last Updated:
- 12/10/2018
Operations
Publications
Patnaik SK, et al. BGMUT: NCBI dbRBC database of allelic variations of genes encoding antigens of blood group systems. Nucleic Acids Res. 2012; 40:D1023-9. doi: 10.1093/nar/gkr958
PMID: 22084196