Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "I"
241 to 250 of 359 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

241
Integrin subunit beta 4
CD104, GP150, JEB5A, JEB5B
Accessory kidney, Adenocarcinoma, Amelogenesis imperfecta, Anemia, Anonychia, Aplasia cutis congenita, Arthrogryposis multiplex congenita, Congenital pyloric atresia, Cystitis, Dental enamel hypoplasia, Dysphagia, Ectodermal dysplasia, Ectropion, Epidermolysis bullosa, Epidermolysis bullosa simplex
View all (27 more)

242
Integrin subunit beta 5
-
Arthritis, Juvenile arthritis, Mental depression, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease, Thyroid diseases

243
Integrin subunit beta 6
AI1H
Alopecia, Alopecia-mental retardation syndrome, Amelogenesis imperfecta, Autoimmune diseases, Brachydactyly, Cholangitis, Dental enamel hypoplasia, Dwarfism, Emphysema, Hypocalcified amelogenesis imperfecta, Hypogonadism, Hypoplastic amelogenesis imperfecta, Ichthyosis, Macrotia, Mental retardation
View all (6 more)

244
Integrin subunit beta 7
-
Prostate cancer

245
Integrin subunit beta 8
-
Asthma, Chronic obstructive pulmonary disease, Endometrioma, Endometriosis, Inflammatory bowel disease, Prostate cancer, Prostate cancer, hereditary

246
Inter-alpha-trypsin inhibitor heavy chain 1
H1P, IATIH, IGHEP1, ITI-HC1, ITIH, SHAP
Anxiety disorder, Bipolar disorder, Knee osteoarthritis, Liver neoplasms, Liver cancer, Manic disorder, Mental depression, Osteoarthritis of hip, Parkinson disease, Schizoaffective disorder, Schizophrenia

247
Inter-alpha-trypsin inhibitor heavy chain 3
H3P, ITI-HC3, SHAP
Anxiety disorder, Attention deficit hyperactivity disorder, Bipolar disorder, Development disorder, Liver carcinoma, Mental depression, Myocardial infarction, Schizophrenia

248
Inter-alpha-trypsin inhibitor heavy chain 4
GP120, H4P, IHRP, ITI-HC4, ITIHL1, PK-120, PK120
Bipolar disorder, Colonic neoplasms, Depressed bipolar disorder, Multiple polyposis syndrome, Schizophrenia

249
IL2 inducible T cell kinase
EMT, LPFS1, LYK, PSCTK2
Anemia, Aphthous ulcer, Gastric cancer, Hodgkin disease, Hypothyroidism, Lymphoproliferative syndrome, Lymphoma, Lymphoproliferative disorder, Metastatic melanoma, Pancytopenia, Respiratory tract diseases, Severe combined immunodeficiency disease, Stomatitis

250
Inosine triphosphatase
C20orf37, DEE35, HLC14-06-P, ITPase, My049, NTPase, dJ794I6.3
Anemia, Brain atrophy, Cerebral atrophy, Developmental delay, Epileptic encephalopathy, Inborn errors of metabolism, Inosine triphosphatase deficiency, Microangiopathic hemolytic anemia, Microcephaly, Neurological disorder with cataract and cardiac involvement, Status epilepticus