811
|
|
|
RNA polymerase III subunit H |
C25, RPC22.9, RPC8 |
|
812
|
|
|
RNA polymerase III subunit K |
C11, C11-RNP3, HLD21, My010, RPC10, RPC11, RPC12.5 |
|
813
|
|
|
RNA polymerase mitochondrial |
APOLMT, COXPD55, MTRNAP, MTRPOL, h-mtRPOL |
|
814
|
|
|
POM121 transmembrane nucleoporin |
P145, POM121A |
|
815
|
|
|
POM121 transmembrane nucleoporin C |
POM121-2 |
|
816
|
|
|
POM121 transmembrane nucleoporin like 12 |
- |
|
817
|
|
|
POM121 transmembrane nucleoporin like 2 |
POM121-L, POM121L |
Angioedema, Asthma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Obstructive pulmonary disease, Inflammatory bowel disease, Insomnia, Lung cancer, Major depressive disorder, Neurotic disorder, Psoriasis, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus type 1 |
818
|
|
|
Proopiomelanocortin |
ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC |
Amnesia, Aortic stenosis, Gouty arthritis, Autism, Bipolar disorder, Body weight, Bradycardia, Calcinosis, Renal cell carcinoma, Cardiomegaly, Cardiomyopathy, Catalepsy, Cerebral hemorrhage, Cerebral palsy, Cholelithiasis, Chondrocalcinosis, Color vision deficiency, Congestive heart failure, Constipation, Cryptogenic west syndrome, Cushing syndrome, Cystitis, Bipolar depression, Major depressive disorder, Diabetes insipidus, Diabetes mellitus, Digestive system disease, Eye disorder, Immune system disorder, Edema, Myoclonic epilepsy, Epilepsy, Tonic-clonic epilepsy, Eye disease, Eye pain, Facial nerve disorder, Fatty liver, Fatty liver, alcoholic, Gastrointestinal disease, Glomerulonephritis, Heart failure, Hematuria, Hemorrhage, Hypercalciuria, Hypertension, Hypertrophic cardiomyopathy, Hypocalcemia, Hypotension, Hypoxia, Immune system disease, Kidney disease, Kidney failure, Liver failure, Long qt syndrome, Melanoma, Metabolic syndrome, Multiple sclerosis, Myasthenia gravis, Myocardial ischemia, Nausea, Necrosis, Obesity, Osteoporosis, Pancreatic diseases, Penile disease, Cushing's disease, Potassium deficiency, Proteinuria, Willis-ekbom disease, Rhabdomyoma, Sacroiliitis, Infantile spasms, Seizures, Sick sinus syndrome, Substance abuse, Synovitis, Diabetes mellitus type 2, Uterine fibroid, West syndromeView all (64 more) |
819
|
|
|
Protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
GNTI.2, GnT I.2, LGMD2O, LGMDR15, MEB, MGAT1.2, RP76, gnT-I.2 |
Autism, Limb girdle muscular dystrophy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital neurologic anomalies, Hydrocephalus, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease, Muscular dystrophy, Optic atrophy, Retinitis pigmentosa, Walker-warburg syndrome |
820
|
|
|
Protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) |
AGO61, C3orf39, GTDC2, MDDGA8, MDDGC8 |
|
