Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6451 to 6460 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6451
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

6452
Iroquois homeobox 6
IRX-3, IRX7, IRXB3
Hypospadias, Ovarian cancer

6453
Iron-sulfur cluster assembly 2
HBLD1, ISA2, MMDS4, c14_5557
Global developmental delay, Mitochondrial disease, Optic atrophy, Diabetes mellitus type 2

6454
Iron-sulfur cluster assembly enzyme
2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU
Mitochondrial disease, Myopathy

6455
ISG15 ubiquitin like modifier
G1P2, IFI15, IMD38, IP17, UCRP, hUCRP
Carcinogenesis, Hepatocellular carcinoma, Major depressive disorder, Glioma, Immunodeficiency

6456
Interferon stimulated exonuclease gene 20
CD25, HEM45
Aortic stenosis, Aortic valve disease, Color vision deficiency, Complex regional pain syndrome, Dupuytren contracture, Hearing loss, Obesity

6457
ISL LIM homeobox 1
ISLET1, Isl-1
Atrial fibrillation, Atrial septal defect, Bladder exstrophy, Bladder exstrophy and epispadias complex, Dilated cardiomyopathy, Congenital heart defects, Congenital heart disease, Diabetes mellitus type 1, Diabetes mellitus type 2, Double outlet right ventricle, Myocardial infarction, Neuroblastoma, Psychiatric disorders, Urinary bladder neoplasms, Ventricular septal defect

6458
ISL LIM homeobox 2
-
Alzheimer disease, Diverticular disease, Scoliosis, Sleep apnea

6459
Immunoglobulin superfamily containing leucine rich repeat
HsT17563, Meflin
Gout, Hodgkin lymphoma, Squamous cell carcinoma

6460
Isthmin 1
C20orf82, ISM, Isthmin, bA149I18.1, dJ1077I2.1
Alzheimer disease, Androgenetic alopecia, Colonic neoplasms, Colorectal cancer, Parkinson disease