ITGA9

Description		integrin subunit alpha 9
Image		No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Integrin Complex Integrin Alpha9-beta1 Complex
	Molecular Function	Collagen Binding Laminin Binding Metal Ion Binding
	Biological Process	Cell Adhesion Integrin-mediated Signaling Pathway Extracellular Matrix Organization 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) Anti-herpes simplex virus 6 IE1A IgG seropositivity ( 33204752) Gut microbiota (bacterial taxa, rank normal transformation method) ( 32572223) Heel bone mineral density ( 30598549) Mortality in sepsis ( 27639821) Nasopharyngeal carcinoma ( 19478819) Phospholipid levels (plasma) ( 22359512) Platelet count ( 32888494) PR interval ( 23139255) Pulse pressure ( 30224653 30578418) Response to antidepressants (symptom improvement) ( 29160301) Systolic blood pressure ( 30578418)
Novel Interacting Genes		1 novel interacting genes: GPX1
Interacting Genes		6 interacting genes: ITGB1 NGF 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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