ITGA9

Description		integrin subunit alpha 9
Image		No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Integrin Complex Basal Plasma Membrane Integrin Alpha9-beta1 Complex
	Molecular Function	Collagen Binding Laminin Binding Metal Ion Binding
	Biological Process	Cell Adhesion Integrin-mediated Signaling Pathway Extracellular Matrix Organization Neutrophil Chemotaxis Wound Healing
Pathways		Integrin cell surface interactions Integrin cell surface interactions ECM proteoglycans Signal transduction by L1
Drugs
Diseases		Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy
GWAS		Amyotrophic lateral sclerosis (sporadic) ( 24529757) Heel bone mineral density ( 30598549) Mortality in sepsis ( 27639821) Nasopharyngeal carcinoma ( 19478819) Phospholipid levels (plasma) ( 22359512) PR interval ( 23139255) Pulse pressure ( 30224653 30578418) Response to antidepressants (symptom improvement) ( 29160301) Systolic blood pressure ( 30578418)
Interacting Genes		6 interacting genes: GPX1 ITGB1 PXN SAT1 SPP1 VEGFD
Entrez ID		3680
HPRD ID		04910
Ensembl ID		ENSG00000144668
Uniprot IDs		Q13797 Q8N6H6
PDB IDs
Enriched GO Terms of Interacting Partners?
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