Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT Adaptive immune defects in a patient with leukocyte adhesion deficiency type III with a novel mutation in FERMT3. 26359933

2016
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT These results indicate that the LAD1v syndrome is caused by truncating mutations in FERMT3. 19064721

2009
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions. 19617577

2009
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT A point mutation in KINDLIN3 ablates activation of three integrin subfamilies in humans. 19234460

2009
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation. 19234463

2009
Entrez Id: 83706
Gene Symbol: FERMT3
FERMT3
CUI: C2748536
Disease: Leukocyte Adhesion Deficiency, Type III
Leukocyte Adhesion Deficiency, Type III 		0.930 GeneticVariation UNIPROT Kindlin-3: a new gene involved in the pathogenesis of LAD-III. 18779414

2008