|
221
|
|
|
Insulin receptor substrate 1 |
HIRS-1 |
Carcinoma of the head and neck, Compensatory hyperinsulinemia, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Endogenous hyperinsulinism, Exogenous hyperinsulinism, Hyperinsulinism, Hyperlipidemia, Liver carcinoma, Obesity, Prostatic neoplasms, Prostate cancer |
|
222
|
|
|
Interferon stimulated exonuclease gene 20 |
CD25, HEM45 |
|
|
223
|
|
|
ISL LIM homeobox 1 |
ISLET1, Isl-1 |
Urinary bladder cancer, Bladder neoplasm, Bladder exstrophy, Bowel incontinence, Congenital exomphalos, Congenital hypoplasia of penis, Congenital malrotation of intestine, Congenital omphalocele, Epispadias, Neuroblastoma, Vesicoureteral reflux |
|
224
|
|
|
Immunoglobulin superfamily containing leucine rich repeat |
HsT17563, Meflin |
|
|
225
|
|
|
Integrin subunit alpha 1 |
CD49a, VLA1 |
|
|
226
|
|
|
Integrin subunit alpha 2 |
BR, CD49B, FMAIT3, GPIa, HPA-5, VLA-2, VLAA2 |
Alloimmune thrombocytopenia, Cerebral palsy, Developmental delay, Endometrioma, Endometriosis, Fetal and neonatal alloimmune thrombocytopenia, Glycoprotein ia deficiency, Hematomas, Retinal vein occlusion, Sensorineural hearing loss, Subarachnoid hemorrhage, Thrombosis of retinal vein |
|
227
|
|
|
Integrin subunit alpha 2b |
BDPLT16, BDPLT2, CD41, CD41B, FMAIT2, GP2B, GPIIb, GT, GT1, GTA, HPA3, PPP1R93 |
Alloimmune thrombocytopenia, Anemia, Arthritis, Carotid artery thrombosis, Cerebral palsy, Common carotid artery thrombosis, Developmental delay, External carotid artery thrombosis, Fetal and neonatal alloimmune thrombocytopenia, Glanzmann thrombasthenia, Hematomas, Internal carotid artery thrombosis, Juvenile arthritis, Leukemia, Macrothrombocytopenia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Sensorineural hearing loss, Still disease, Stroke, Subarachnoid hemorrhage, ThrombastheniaView all (7 more) |
|
228
|
|
|
Integrin subunit alpha 3 |
CD49C, FRP-2, GAP-B3, GAPB3, ILNEB, JEB7, MSK18, VCA-2, VL3A, VLA3a |
Congenital alveolar dysplasia, Epidermolysis bullosa simplex, Glomerulosclerosis, Gynecomastia, Hypoalbuminemia, Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa,, Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital, Junctional epidermolysis bullosa, Lung diseases, Macrotia, Microcephaly, Microstomia, Nail dystrophy, Narcolepsy, Nephrotic syndrome, Onycholysis, Renal insufficiencyView all (2 more) |
|
229
|
|
|
Integrin subunit alpha 4 |
CD49D, IA4 |
|
|
230
|
|
|
Integrin subunit alpha 5 |
CD49e, FNRA, VLA-5, VLA5A |
|
