|
111
|
|
|
MAP3K14 antisense RNA 1 |
- |
|
|
112
|
|
|
Potassium inwardly rectifying channel subfamily J member 18 |
KIR2.6, TTPP2 |
Atrioventricular block, Graves disease, Hyperthyroidism, Hypokalemic periodic paralysis, Obesity, Periodic hypokalemic paresis, Periodic paralysis, Quadriplegia, Thyrotoxic periodic paralysis, Thyrotoxicosis with toxic single thyroid nodule, Toxic goiter, Ventricular fibrillation |
|
113
|
|
|
Phospholipase A2 group IVB |
HsT16992, cPLA2-beta |
|
|
114
|
|
|
Histone deacetylase 5 |
HD5, NY-CO-9 |
Adjustment disorders, Bipolar disorder, Manic disorder, Mental depression, Osteoporosis, Pulmonary arterial hypertension, Pulmonary hypertension, Pulmonary hypertension with hereditary hemorrhagic telangiectasia, Reactive depression, Scleroderma, Transient situational disturbance |
|
115
|
|
|
Killin, p53 regulated DNA replication inhibitor |
CWS4, KILLIN |
Adenoma sebaceum, Autism, Brachydactyly, Breast cancer, Breast carcinoma, Cafe-au-lait spot, Cataract, Congenital pectus excavatum, Conjunctival hamartoma, Cowden syndrome, Developmental delay, Dwarfism, Endometrial carcinoma, Enlarged polycystic ovaries, Follicular thyroid carcinoma, Gynecomastia, Hamartoma, Hamartomatous polyposis, Hemangioma, cavernous, Hereditary breast cancer, High palate, Impaired cognition, Kidney neoplasm, Lipoma, Macrocephaly, Macroglossia, Melanocytic nevus, Melanoma, Meningioma, Mental retardation, Myopia, Palmoplantar keratoderma, Papilloma, Polyp of large intestine, Renal carcinoma, Scoliosis, TrichilemmomaView all (22 more) |
|
116
|
|
|
TMCO1 antisense RNA 1 |
- |
|
|
117
|
|
|
Programmed cell death 6 interacting protein |
AIP1, ALIX, DRIP4, HP95, MCPH29 |
|
|
118
|
|
|
RNA, U4atac small nuclear |
LWS, MOPD1, RFMN, RNU4ATAC1, TALS, U4ATAC |
Agenesis of corpus callosum, Alopecia, Aortic coarctation, Asthma, Astigmatism, Atrial septal defect, Brachydactyly, Camptodactyly of fingers, Cerebellar vermis agenesis, Dislocated radial head, Short femur, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Eczema, Elbow flexion contracture, Eosinophilia, Epiphyseal dysplasia, Gastritis, Gastroparesis, Glaucoma, Hip contracture, Hydronephrosis, Hyperkeratosis, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Hypotrichosis, Lowry wood syndrome, Mental retardation, Microcephalic osteodysplastic primordial dwarfism, Microcephaly, Micrognathism, Micromelia, Microtia, Neuronal heterotopia, Noncompaction cardiomyopathy, Nystagmus, Osteopenia, Osteoporosis, Otitis media, Pachygyria, Penis agenesis, Platelet-type bleeding disorder, Posteriorly rotated ear, Proptosis, Renal cyst, Renal hypoplasia, Respiratory failure, Retinal dystrophy, Rickets, Roifman syndrome, Salaam seizures, Seizure, Shoulder flexion contracture, Specific learning disorder, Spondyloepiphyseal dysplasia, Status epilepticus, Submucosal cleft palate, Tetralogy of fallotView all (45 more) |
|
119
|
|
|
Programmed cell death 6 |
ALG-2, ALG2, PEF1B |
|
|
120
|
|
|
Small NF90 (ILF3) associated RNA I |
snaR-3 |
|
