361
|
|
|
Iroquois homeobox 3 |
IRX-1, IRXB1 |
|
362
|
|
|
Iroquois homeobox 4 |
IRXA3 |
|
363
|
|
|
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 |
364
|
|
|
Iroquois homeobox 6 |
IRX-3, IRX7, IRXB3 |
|
365
|
|
|
Iron-sulfur cluster assembly 2 |
HBLD1, ISA2, MMDS4, c14_5557 |
|
366
|
|
|
Iron-sulfur cluster assembly enzyme |
2310020H20Rik, HML, ISU2, NIFU, NIFUN, hnifU |
|
367
|
|
|
ISG15 ubiquitin like modifier |
G1P2, IFI15, IMD38, IP17, UCRP, hUCRP |
|
368
|
|
|
Interferon stimulated exonuclease gene 20 |
CD25, HEM45 |
|
369
|
|
|
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 |
370
|
|
|
ISL LIM homeobox 2 |
- |
|