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HLA-B47 antigen

Also Known As:

HLA B47; HLA B4701; HLA B4702; HLA Bw47; HLA Bw47 antigen; HLA-B47; HLA-B4701; HLA-B4702; HLA-B47:01 antigen; HLA-B47:02 antigen; HLA-Bw47

Networked: 2 relevant articles (0 outcomes, 1 trials/studies)

Bio-Agent Context: Research Results

Carbohydrates: 22023
- Glycoconjugates: 1353
  - Glycoproteins: 24834
    - Membrane Glycoproteins: 2252
      - Histocompatibility Antigens Class I: 1944
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Glycoproteins: 24834
    - Membrane Glycoproteins: 2252
      - Histocompatibility Antigens Class I: 1944
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
  - Membrane Proteins: 10078
    - Membrane Glycoproteins: 2252
      - Histocompatibility Antigens Class I: 1944
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
Biological Factors: 2472
- Antigens: 143924
  - Surface Antigens: 5813
    - Histocompatibility Antigens: 1132
      - HLA Antigens: 8934
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
      - Histocompatibility Antigens Class I: 1944
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
  - Isoantigens: 1221
    - Histocompatibility Antigens: 1132
      - HLA Antigens: 8934
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2
      - Histocompatibility Antigens Class I: 1944
        HLA-B Antigens: 1869
        HLA-B47 antigen: 2

Related Diseases

1.	Congenital adrenal hyperplasia due to 21 hydroxylase deficiency 01/01/1988 - "Adrenal 21-hydroxylase deficiency is strongly associated with HLA-Bw47. " 01/01/1988 - "Comparison of the structure of HLA-Bw47 to HLA-B13 and its relationship to 21-hydroxylase deficiency." 11/01/1987 - "Our studies demonstrate that 1) HLA-Bw47 is not an invariant marker for salt-losing CAH due to 21-hydroxylase deficiency, and 2) the HLA-Bw47 phenotype coupled to CAH is not derived from the HLA-B13 genotype by a single mutation." 11/01/1987 - "HLA-Bw47, a rare human histocompatibility antigen, occurs in strong linkage disequilibrium with HLA-A3,Cw6,DR7 and salt-losing congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and is associated with a contiguous deletion of the active CA21HB gene and the C4B complement gene. "
2.	Congenital Adrenal Hyperplasia (Hyperplasia, Congenital Adrenal) 11/01/1987 - "HLA-Bw47, a rare human histocompatibility antigen, occurs in strong linkage disequilibrium with HLA-A3,Cw6,DR7 and salt-losing congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency and is associated with a contiguous deletion of the active CA21HB gene and the C4B complement gene. "

Related Drugs and Biologics

1.	HLA-B13 Antigen
2.	Salts
3.	Complement C4b
4.	Histocompatibility Antigens (Histocompatibility Antigen)