Source: LHGDN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 567
Gene Symbol: B2M
B2M
CUI: C0025202
Disease: melanoma
melanoma 		0.100 AlteredExpression LHGDN The coincidence of chromosome 15 aberrations and beta2-microglobulin gene mutations is causative for the total loss of human leukocyte antigen class I expression in melanoma. 16740750

2006
Entrez Id: 567
Gene Symbol: B2M
B2M
CUI: C0025202
Disease: melanoma
melanoma 		0.100 AlteredExpression LHGDN Complete loss of HLA class I antigen expression on melanoma cells: a result of successive mutational events. 12516095

2003