UNC119, unc-119 lipid binding chaperone, 9094

N. diseases: 33; N. variants: 1
Disease: IMMUNODEFICIENCY 13 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		0.620 GeneticVariation disease UNIPROT The V22G mutation of Unc119 represents a novel genetic defect in ICL. 22184408 2012
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		0.620 GeneticVariation disease BEFREE The V22G mutation of Unc119 represents a novel genetic defect in ICL. 22184408 2012
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		0.620 Biomarker disease GENOMICS_ENGLAND The V22G mutation of Unc119 represents a novel genetic defect in ICL. 22184408 2012
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		0.620 GermlineCausalMutation disease ORPHANET The V22G mutation of Unc119 represents a novel genetic defect in ICL. 22184408 2012
CUI: C3809768
Disease: IMMUNODEFICIENCY 13
IMMUNODEFICIENCY 13 		0.620 GeneticVariation disease BEFREE Here we review our recent findings on the UNC119 mutation in ICL. 22729960 2012