881
|
|
|
IMPA2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
882
|
|
|
Impact RWD domain protein |
RWDD5 |
Curated: Bipolar disorder, Major depressive disorder, Nasopharyngeal neoplasms
Unreviewed: Anaplastic thyroid cancer, Aphasia, Asthma, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Breast Cancer, Cardiovascular Diseases, Chronic Obstructive Pulmonary Disease, Colorectal Cancer, Congenital Heart Disease, Congestive Heart Failure, Coronary Heart Disease, Crohn Disease, Diabetes, Diabetes Mellitus, Heart Diseases, Heart Failure, Hemophilia, Hypertension, Inflammatory Bowel Disease, Ischemic Stroke, Learning Disorders, Lung carcinoma, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphocytic Leukemia, Major Affective Disorder, Malignant Neoplasm, Mental Depression, Migraine, Neoplasms, Obesity, Papillary thyroid carcinoma, Phyllodes Tumor, Portal Hypertension, Prostate cancer, Psoriatic Arthritis, Rhegmatogenous retinal detachment, Rheumatoid arthritis, Sarcoma, Skin Erosion, Stomach Carcinoma, Stomach Neoplasms, Stress Disorder, Stroke, Ulcerative colitis
|
883
|
|
|
Inosine monophosphate dehydrogenase 1 |
IMPD, IMPD1, IMPDH-I, LCA11, RP10, sWSS2608 |
Curated: Leber congenital amaurosis, Pelvic organ prolapse, Retinitis pigmentosa, Thyroiditis, IMPDH1-related retinopathy
Unreviewed: Age-related macular degeneration, Breast Cancer, Breast Carcinoma, Breast neoplasm, Cataract, Ciliopathies, Color vision deficiency, Colorectal neoplasm, Congenital blindness, Congenital Cerebral Hernia, Congenital Hypoplasia Of Penis, Cyclic neutropenia, Deficiency Of Phosphoglycerate Kinase, Developmental Delay, Diabetes, Diabetes Mellitus, Dilated cardiomyopathy, Disorder Of Eye, Dysgenesis Neuroepithelialis Retinae, Geographic Atrophy, Glaucoma, Graft-versus-host disease, Hearing Loss, Heart failure, Hemiplegia/hemiparesis, Hepatocellular carcinoma, Hyperinsulinism, Hypogonadism, Inflammatory Bowel Disease, Keratoconus, Leber Congenital Amaurosis, Leukopenia, Lymphopenia, Macular Degeneration, Malformation of cortical development, Mental retardation, Myeloid leukemia, Neutropenia, Nyctalopia, Nystagmus, Obesity, Optic Atrophy, Optic neuritis, Phosphoglycerate Kinase 1 Deficiency, Renal cell carcinoma, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinitis Pigmentosa, Rod-cone dystrophy, Stargardt disease, Urinary bladder neoplasms
|
884
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 1 |
bA537H15.4 |
Curated: N/A
Unreviewed: N/A
|
885
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 10 |
- |
Curated: N/A
Unreviewed: N/A
|
886
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 11 |
IMPDH1, IMPDHL1 |
Curated: N/A
Unreviewed: N/A
|
887
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
888
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
889
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 4 |
- |
Curated: N/A
Unreviewed: N/A
|
890
|
|
|
Inosine monophosphate dehydrogenase 1 pseudogene 5 |
- |
Curated: N/A
Unreviewed: N/A
|