Gene: ITGA7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3679
Gene Symbol: ITGA7
ITGA7 		0.510 Biomarker disease MGD α6β1 and α7β1 integrins are required in Schwann cells to sort axons. 24227711 2013
Entrez Id: 3679
Gene Symbol: ITGA7
ITGA7 		0.510 GeneticVariation disease BEFREE Mutation in MYH7B causes a classical LVNC phenotype, whereas mutation in ITGA7 causes CFTD. 23800289 2013
Entrez Id: 3679
Gene Symbol: ITGA7
ITGA7 		0.510 GermlineCausalMutation disease ORPHANET Mutation in MYH7B causes a classical LVNC phenotype, whereas mutation in ITGA7 causes CFTD. 23800289 2013
Entrez Id: 3679
Gene Symbol: ITGA7
ITGA7 		0.510 Biomarker disease MGD Defective integrin switch and matrix composition at alpha 7-deficient myotendinous junctions precede the onset of muscular dystrophy in mice. 12588796 2003
Entrez Id: 3679
Gene Symbol: ITGA7
ITGA7 		0.510 Biomarker disease MGD Absence of integrin alpha 7 causes a novel form of muscular dystrophy. 9354797 1997