|
831
|
|
|
MicroRNA 656 |
MIRN656, hsa-mir-656, mir-656 |
|
|
832
|
|
|
Mucin 5B, oligomeric mucus/gel-forming |
MG1, MUC-5B, MUC5, MUC9 |
Bronchiectasis, Cirrhosis, Diffuse interstitial pulmonary fibrosis, Diffuse panbronchiolitis, Gastroesophageal reflux disease, Honeycomb lung, Lung adenocarcinoma, Lung diseases, Mental depression, Pulmonary arterial hypertension, Pulmonary fibrosis, Hamman-rich syndrome |
|
833
|
|
|
Meiotic kinetochore factor |
SPO13 |
|
|
834
|
|
|
MEIS1 antisense RNA 3 |
- |
|
|
835
|
|
|
Mitochondrial ribosomal protein L49 |
C11orf4, COXPD60, L49mt, MRP-L49, NOF, NOF1, mL49 |
|
|
836
|
|
|
Metallophosphoesterase domain containing 2 |
239FB, C11orf8 |
|
|
837
|
|
|
Myelin regulatory factor |
11orf9, C11orf9, CUGS, MMERV, MRF, NNO1, Ndt80, pqn-47 |
Ambiguous genitalia, Ankylosing spondylitis, Asthma, Atrial septal defect, Bronchomalacia, Cardiac-urogenital syndrome, Cholangitis, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Congenital diaphragmatic hernia, Pulmonary hypoplasia, Congenital malrotation of intestine, Congenital total pulmonary venous return anomaly, Crohn disease, Cryptorchidism, Dextrocardia, Encephalitis/encephalopathy with reversible myelin vacuolization, Gonadal hypoplasia, High palate, Horseshoe kidney, Hydronephrosis, Hypoplastic left heart syndrome, Kidney disease, Kidney failure, Lung cancer, Microphthalmos, Moyamoya disease, Muscular ventricular septal defect, Nasal polyposis, Patent ductus arteriosus, Penile hypospadias, Penis agenesis, Persistent umbilical sinus, Polycythemia, Psoriasis, Respiratory tract diseases, Scimitar syndrome, Tetralogy of fallot, Ulcerative colitis, Ventricular septal defectView all (27 more) |
|
838
|
|
|
Myeloid zinc finger 1 |
MZF-1, MZF1B, ZFP98, ZNF42, ZSCAN6 |
|
|
839
|
|
|
Makorin ring finger protein 3 |
CPPB2, D15S9, RNF63, ZFP127, ZNF127 |
Acromicria, Acromicric dysplasia, Attention deficit hyperactivity disorder, Central precocious puberty, Clinodactyly, Colorectal cancer, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Hyperinsulinism, Hyperopia, Hypogonadotropic hypogonadism, Isolated somatotropin deficiency, Motor delay, Hypotonia, Penis agenesis, Physiologic amenorrhea, Prader-willi syndrome, Precocious pubarche, Precocious puberty, Royer syndrome, Scoliosis, Sleep apnea, Somatotropin deficiency, Specific learning disorder, TestotoxicosisView all (12 more) |
|
840
|
|
|
MicroRNA 758 |
MIRN758, hsa-mir-758, mir-758 |
|
