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
Showing genes starting with "I"
361 to 370 of 438 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

361
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
View all (1 more)

362
Iroquois homeobox 2
IRXA2
Central nervous system cancer, Clear cell sarcoma of kidney, Glioblastoma, Glioma, Lung disease, Obesity

363
Iroquois homeobox 3
IRX-1, IRXB1
Color vision deficiency, Eosinophilia, Lung disease, Prostate cancer, Schizophrenia, Diabetes mellitus type 2

364
Iroquois homeobox 4
IRXA3
Adenoid cystic carcinoma, Cardiovascular disease, Congenital heart disease, Salivary gland neoplasms, Tetralogy of fallot, Ventricular septal defect

365
Iroquois homeobox 5
HMMS, IRX-2a, IRXB2
Hypochromic microcytic anemia, Anodontia, Congenital heart defects, Craniofacial abnormalities, Craniofacial dysplasia osteopenia syndrome, Tooth agenesis, Facial dysmorphism syndrome, Frontonasal dysplasia, Congenital heart defect, Hyperopia, Lung disease, Myopia, Otosclerosis, Hearing loss

366
Iroquois homeobox 6
IRX-3, IRX7, IRXB3
Hypospadias, Ovarian cancer

367
Iron-sulfur cluster assembly 2
HBLD1, ISA2, MMDS4, c14_5557
Global developmental delay, Mitochondrial disease, Optic atrophy, Diabetes mellitus type 2

368
Iron-sulfur cluster assembly enzyme
2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU
Mitochondrial disease, Myopathy

369
ISG15 ubiquitin like modifier
G1P2, IFI15, IMD38, IP17, UCRP, hUCRP
Carcinogenesis, Hepatocellular carcinoma, Major depressive disorder, Glioma, Immunodeficiency

370
Interferon stimulated exonuclease gene 20
CD25, HEM45
Aortic stenosis, Aortic valve disease, Color vision deficiency, Complex regional pain syndrome, Dupuytren contracture, Hearing loss, Liver cirrhosis, Obesity