Source: MGD

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 63915
Gene Symbol: BLOC1S5
BLOC1S5
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		0.200 Biomarker MGD Gravity receptor function in mice with graded otoconial deficiencies. 15109702

2004
Entrez Id: 63915
Gene Symbol: BLOC1S5
BLOC1S5
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		0.200 Biomarker MGD Characterization of melanosomes in murine Hermansky-Pudlak syndrome: mechanisms of hypopigmentation. 15009730

2004
Entrez Id: 63915
Gene Symbol: BLOC1S5
BLOC1S5
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		0.200 Biomarker MGD The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. 11912185

2002
Entrez Id: 63915
Gene Symbol: BLOC1S5
BLOC1S5
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		0.200 Biomarker MGD Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha. 1912584

1991
Entrez Id: 63915
Gene Symbol: BLOC1S5
BLOC1S5
CUI: C0032197
Disease: Platelet Storage Pool Deficiency
Platelet Storage Pool Deficiency 		0.200 Biomarker MGD Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV. 5367369

1969