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

Documentation