Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6441 to 6450 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6441
Interferon regulatory factor 9
IRF-9, ISGF3, ISGF3G, p48
Alzheimer disease, Immunodeficiency

6442
Immunity related GTPase cinema
CINEMA, IFGGE, IRGC1, Iigp5, R30953_1
Alzheimer disease, Dementia

6443
Immunity related GTPase M
IBD19, IFI1, IRGM1, LRG-47, LRG47
Ankylosing spondylitis, B-cell acute lymphoblastic leukemia, Ulcerative colitis, Crohn disease, Inflammatory bowel disease, Psoriasis, Rheumatoid arthritis, Sclerosing cholangitis

6444
Insulin receptor substrate 1
HIRS-1
Alzheimer disease, Hepatocellular carcinoma, Ischemic heart disease, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Hyperinsulinism, Hyperlipidemia, Hyperlipoproteinemia, Myocardial ischemia, Nasopharyngeal neoplasms, Obesity, Oligodendroglioma, Prostatic neoplasms, Scoliosis
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6445
Insulin receptor substrate 2
IRS-2
Hepatocellular carcinoma, Diabetes mellitus type 2, Hyperglycemia, Medulloblastoma, Parkinson disease, Prostate cancer, Stomach neoplasms

6446
Insulin receptor substrate 4
CHNG9, IRS-4, PY160
Basal cell carcinoma

6447
Iroquois homeobox 1
IRX-5, IRXA1
Alzheimer disease, Basal cell carcinoma, Cardiovascular disease, Congenital heart defects, Coronary artery disease, Insomnia, Keratoconus, Lung disease, Myocardial infarction, Optic atrophy, Oropharyngeal cancer, Peripheral neuropathy, Peripheral vascular disease, Raynaud disease, Scoliosis
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6448
Iroquois homeobox 2
IRXA2
Central nervous system cancer, Clear cell sarcoma of kidney, Glioblastoma, Glioma, Lung disease, Obesity

6449
Iroquois homeobox 3
IRX-1, IRXB1
Color vision deficiency, Eosinophilia, Lung disease, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

6450
Iroquois homeobox 4
IRXA3
Adenoid cystic carcinoma, Cardiovascular disease, Congenital heart disease, Salivary gland neoplasms, Tetralogy of fallot, Ventricular septal defect