Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
6481 to 6490 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6481
Integrin subunit alpha L
CD11A, LFA-1, LFA1A
Ankylosing spondylitis, Behcet disease, Obstructive pulmonary disease, Depression, Crohn disease, Pharyngeal disorder, Gastroesophageal reflux disease, Inflammatory bowel disease, Promyelocytic leukemia, Metabolic syndrome, Psoriasis, Respiratory system disease, Sclerosing cholangitis, Smooth surface dental caries, Diabetes mellitus type 2
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6482
Integrin subunit alpha M
CD11B, CR3A, MAC-1, MAC1A, MO1A, SLEB6
Autoimmune musculoskeletal system disorder, Bipolar disorder, Cutaneous lupus erythematosus, Allergic contact dermatitis, Hearing loss, Hyperglycemia, Hyperinsulinism, Iga nephropathy, Diabetes mellitus type 2, Promyelocytic leukemia, Systemic lupus erythematosus, Lupus nephritis, Obesity, Schizophrenia, Systemic sclerosis

6483
Integrin subunit alpha V
CD51, MSK8, VNRA, VTNR
Asthma, Cerebral hemorrhage, Cerebrovascular disorder, Color vision deficiency, Crohn disease, Dyslexia, Inflammatory bowel disease, Stroke, Ulcerative colitis

6484
Integrin subunit alpha X
CD11C, SLEB6
Alzheimer disease, Iga nephropathy, Promyelocytic leukemia, Systemic lupus erythematosus

6485
Integrin subunit beta 1
CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA, VLAB
Brain injuries, Calcinosis, Non-small-cell lung carcinoma, Squamous cell carcinoma, Cardiomyopathy, Dilated cardiomyopathy, Congestive heart failure, Endometriosis, Esophageal atresia, Heart failure, Neural tube defect

6486
Integrin subunit beta 1 binding protein 1
ICAP-1A, ICAP-1B, ICAP-1alpha, ICAP1, ICAP1A, ICAP1B
Alzheimer disease, Bone disease, Craniofacial abnormalities, Oligodendroglioma

6487
Integrin subunit beta 2
CD18, LAD, LCAMB, LFA-1, MAC-1, MF17, MFI7
Behcet disease, Brain neoplasms, Calcinosis, Chloracne, Skin ulcer, Congenital leukocyte adherence deficiency, Coronary restenosis, Dermatitis, Heart valve disease, Heart valve prolapse, Hypersensitivity, Promyelocytic leukemia, Leukocyte adhesion deficiency, Leukocyte disorders, Nephrotic syndrome
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6488
Integrin subunit beta 3
BDPLT16, BDPLT2, BDPLT24, CD61, FMAIT1, GP3A, GPIIIa, GT, GT2
Alzheimer disease, Asthma, Autism, Autoimmune disease, Macrothrombocytopenia, Platelet-type bleeding disorder, Platelet disorder, Bone fracture, Carotid artery thrombosis, Cerebral hemorrhage, Cerebrovascular disorder, Coronary thrombosis, Crohn disease, Diverticular disease, Glanzmann thrombasthenia
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6489
Integrin subunit beta 3 binding protein
CENP-R, CENPR, HSU37139, NRIF3, TAP20
Endometriosis, Nonalcoholic fatty liver disease, Diabetes mellitus type 2

6490
Integrin subunit beta 4
CD104, GP150, JEB5A, JEB5B
Aplasia cutis congenita, Adenoid cystic carcinoma, Non-small-cell lung carcinoma, Galactokinase deficiency, Ectodermal dysplasia, Epidermolysis bullosa, Junctional epidermolysis bullosa, Focal glomerulosclerosis, Multiple sclerosis, Nephrotic syndrome, Neurodevelopmental disorder, Ocular hypertension, Other epidermolysis bullosa, Salivary gland neoplasms, Weber-cockayne syndrome