BGMUT: NCBI dbRBC database of allelic variations of genes encoding antigens of blood group systems

Nucleic Acids Research

Volumn 40, Issue D1, 2012, Pages

  Patnaik, Santosh Kumar ^a   Helmberg, Wolfgang ^b   Blumenfeld, Olga O ^c  

^a ROSWELL PARK CANCER INSTITUTE   (United States)

^b MEDICAL UNIVERSITY OF GRAZ   (Austria)

^c ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HLA ANTIGEN;

ALLELE; ARTICLE; BGMUT DATA BASE; BLOOD GROUP SYSTEM; CELL MEMBRANE; ERYTHROCYTE; ETHNICITY; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC DATABASE; GENETIC VARIABILITY; HUMAN; ONLINE SYSTEM; PRIORITY JOURNAL;

ALLELES; BLOOD GROUP ANTIGENS; DATABASES, GENETIC; GENETIC VARIATION; HUMANS;

EID: 84862238137     PISSN: 03051048     EISSN: 13624962     Source Type: Journal    
DOI: 10.1093/nar/gkr958     Document Type: Article

References (11)

1. Sayers,E.W., Barrett,T., Benson,D.A., Bolton,E., Bryant,S.H., Canese,K., Chetvernin,V., Church,D.M., DiCuccio,M., Federhen,S. et al. (2011) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res., 39, D38-D51.
2. Broadberry,R.E. and Lin,M. (1996) The distribution of the MiIII (Gp.Mur) phenotype among the population of Taiwan. Transfus. Med., 6, 145-148. (Pubitemid 126427093)
3. Claustres,M., Horaitis,O., Vanevski,M. and Cotton,R.G. (2002) Time for a unified system of mutation description and reporting: a review of locus-specific mutation databases. Genome Res., 12, 680-688. (Pubitemid 34546456)
4. Blumenfeld,O.O. and Patnaik,S.K. (2004) Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum. Mutat., 23, 8-16. (Pubitemid 38056096)
5. Giardine,B., Riemer,C., Hefferon,T., Thomas,D., Hsu,F., Zielenski,J., Sang,Y., Elnitski,L., Cutting,G., Trumbower,H. et al. (2007) PhenCode: connecting ENCODE data with mutations and phenotype. Hum. Mutat., 28, 554-562. (Pubitemid 46744285)
6. Storry,J.R., Castilho,L., Daniels,G., Flegel,W.A., Garratty,G., Francis,C.L., Moulds,J.M., Moulds,J.J., Olsson,M.L., Poole,J. et al. (2011) International Society of Blood Transfusion Working Party on red cell immunogenetics and blood group terminology: Berlin report. Vox Sang., 101, 77-82.
7. Patnaik,S.K. and Blumenfeld,O.O. (2011) Patterns of human genetic variation inferred from comparative analysis of allelic mutations in blood group antigen genes. Hum. Mutat., 32, 263-271.
8. Hamosh,A., Scott,A.F., Amberger,J.S., Bocchini,C.A. and McKusick,V.A. (2005) Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res., 33, D514-D517. (Pubitemid 40207927)
9. Wang,Y., Geer,L.Y., Chappey,C., Kans,J.A. and Bryant,S.H. (2000) Cn3D: sequence and structure views for Entrez. Trends Biochem. Sci., 25, 300-302. (Pubitemid 30333390)
10. Helmberg,W., Dunivin,R. and Feolo,M. (2004) The sequencing-based typing tool of dbMHC: typing highly polymorphic gene sequences. Nucleic Acids Res., 32, W173-W175. (Pubitemid 38997323)
11. Robinson,J., Mistry,K., McWilliam,H., Lopez,R., Parham,P. and Marsh,S.G. (2011) The IMGT/HLA database. Nucleic Acids Res., 39, D1171-D1176.