591
|
|
|
ER membrane protein complex subunit 7 |
C11orf3, C15orf24, HT022, ORF1-FL1 |
Curated: N/A
Unreviewed: Cardiomyopathy, Sickle cell anemia
|
592
|
|
|
ER membrane protein complex subunit 8 |
C16orf2, C16orf4, COX4NB, FAM158B, NOC4 |
Curated: Diabetes mellitus type 2
Unreviewed: Myocardial Infarction
|
593
|
|
|
ER membrane protein complex subunit 9 |
C14orf122, CGI-112, FAM158A |
Curated: N/A
Unreviewed: N/A
|
594
|
|
|
Endomucin |
EMCN2, MUC14 |
Curated: Appendicitis, Attention deficit hyperactivity disorder, Cerebral amyloid angiopathy, Eosinophilia, Insomnia, Iron metabolism disorder, Major depressive disorder, Metabolic syndrome, Colorectal adenoma, Mood disorder, Open angle glaucoma, Stroke
Unreviewed: Breast neoplasm, Cutaneous lupus erythematosus, Dermatitis, Dermatologic Disorders, Diabetes, Diabetes Mellitus, Diabetic Retinopathy, Eczema, Follicular thyroid cancer, Hemangioma, Hemangiosarcoma, Hepatocellular carcinoma, Hyperglycemia, Idiopathic pulmonary fibrosis, Lung neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Mental Depression, Mood Disorder, Neoplasms, Osteopenia, Psoriasis, Renal cell carcinoma, Rheumatoid arthritis, Sarcoma, T-Cell Lymphoma
|
595
|
|
|
Emerin |
EDMD, LEMD5, STA |
Curated: Cardiomyopathy, Dilated cardiomyopathy, Emery-dreifuss muscular dystrophy, Heart disease, Hereditary motor and sensory neuropathies, Hypertrophic cardiomyopathy, Myopathy, Neuromuscular disease, X-linked emery-dreifuss muscular dystrophy
Unreviewed: Abnormal Involuntary Movement, Activated Protein C Resistance, Aneuploidy, Antiphospholipid Syndrome, Arthritis, Atrial Fibrillation, Atrioventricular block, Autoimmune Polyendocrinopathy, Benign scapuloperoneal muscular dystrophy with cardiomyopathy, Brain Neoplasms, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiac arrhythmias, Cardiovascular abnormalities, Cerebral Aneurysm, Cerebral Angiitis, Cerebral Infarction, Cerebral Ischemia, Congenital Anomaly Of Neck, Congenital heart defect, Congenital heart defects, Congenital myopathy, Congenital Pectus Excavatum, Congestive Heart Failure, Disorder Of Skeletal Muscle, Duchenne Muscular Dystrophy, Dyskinetic Syndrome, Dystonia, Ectrodactyly, Eichsfeld type congenital muscular dystrophy, Elbow flexion contracture, Emery dreifuss muscular dystrophy, Emery-Dreifuss Muscular Dystrophy, Emery-Dreifuss Muscular Dystrophy, X-Linked, Ewing sarcoma, Facioscapulohumeral Muscular Dystrophy, Gingival Recession, Graft-Vs-Host Disease, Graves Disease, Hearing loss with stapes fixation, Heart Block, Heart Diseases, Heart Failure, Hemophagocytic Lymphohistiocytosis, Hemophilia, Hypertension, Ichthyosis, Impaired Cognition, Inclusion Body Myositis, Left ventricular noncompaction, Leukemia, Limb-Girdle Muscular Dystrophy, Lipodystrophy, Lung adenocarcinoma, Lung carcinoma, Lupus anticoagulant, Malignant Neoplasm, Mental Depression, Metabolic Diseases, Mitochondrial disease, Moyamoya Disease, Muscular dystrophy, Myopathy With Excessive Autophagy, X-Linked, Myositis, Neoplasms, Neuromuscular Diseases, Obesity, Ovarian neoplasm, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Papillary thyroid cancer, Parkinson Disease, Premature aging, Prostate cancer, Prostatic neoplasm, Pseudoxanthoma elasticum, Ptosis, Pulsatile Tinnitus, Rectal Carcinoma, Rheumatoid arthritis, Sarcoglycanopathy, Scoliosis, Sick sinus syndrome, Sinus Node Dysfunction, Sprengel Deformity, Thrombosis, Ventricular Fibrillation, Vocal Cord Paralysis
|
596
|
|
|
Essential meiotic structure-specific endonuclease 1 |
MMS4L, SLX2A |
Curated: N/A
Unreviewed: Brain neoplasms, Carcinogenesis, Chromosomal instability, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Glioblastoma, Lung neoplasms, Lymphatic metastasis, Malignant Neoplasm, Neoplasms, Renal cell carcinoma, Stomach neoplasms, Triple negative breast cancer
|
597
|
|
|
Essential meiotic structure-specific endonuclease subunit 2 |
SLX2B, gs125 |
Curated: Combined oxidative phosphorylation deficiency, Mitochondrial disease
Unreviewed: Combined Oxidative Phosphorylation Deficiency, Leigh Syndrome, Prostatic neoplasm
|
598
|
|
|
EMG1 N1-specific pseudouridine methyltransferase |
C2F, Grcc2f, NEP1 |
Curated: Bowen-conradi syndrome
Unreviewed: Adenocarcinoma, Bowen-Conradi Syndrome, Camptodactyly of fingers, Carcinosarcoma, Cirrhosis, Cryptorchidism, Development Disorder, Developmental disability, Dwarfism, Endometrial Cancer, Endometrioid cancer, Ewing sarcoma, Microcephaly, Micrognathism, Neoplasms, Nephroblastoma, Neural Tube Defect, Oral cleft, Sarcoma, Scleroderma, Stroke, Vertical Talus, Wilms tumor
|
599
|
|
|
EQTN MOB3B IFNK C9orf72 enhancer RNA I |
- |
Curated: N/A
Unreviewed: N/A
|
600
|
|
|
EMI domain containing 1 |
EMI5, EMU1 |
Curated: Breast cancer, Clear cell renal cell carcinoma, Kidney cancer, Open angle glaucoma, Upper aerodigestive tract neoplasm
Unreviewed: Breast Cancer, Breast Carcinoma
|