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12211
|
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TNF superfamily member 15 |
TL1, TL1A, TNLG1B, VEGI, VEGI192A |
Ankylosing spondylitis, Arthritis, Asthma, Autoimmune diseases, Autoimmune thyroiditis, Biliary cholangitis, Biliary cirrhosis, Celiac disease, Cirrhosis, Common variable immunodeficiency, Conjugated hyperbilirubinemia, Crohn disease, Dermatographic urticaria, Diabetes mellitus, Enteritis, Gastrointestinal inflammation, Hypoalbuminemia, Inflammatory bowel disease, Leprosy, Liver carcinoma, Liver failure, Liver fibrosis, Lupus erythematosus, Multiple sclerosis, Osteoarthrosis deformans, Osteoporosis, Portal hypertension, Psoriasis, Ulcerative colitisView all (14 more) |
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12212
|
|
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Mediator complex subunit 12 |
ARC240, CAGH45, FGS1, HDKR, HOPA, Kto, MED12S, OHDOX, OKS, OPA1, TNRC11, TRAP230 |
Adrenocortical carcinoma, Agenesis of corpus callosum, Aortic coarctation, Arachnodactyly, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Blepharophimosis, Blepharophimosis-mental retardation syndrome, Brachycephaly, Brachydactyly, Breast cancer, Mammary neoplasms, Breast carcinoma, Choanal atresia, Clinodactyly, Congenital camptodactyly, Congenital epicanthus, Congenital exomphalos, Congenital heart defects, Congenital malrotation of intestine, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Dysmorphic features, Facial paralysis, Fg syndrome, Fibroadenoma, Frontal bossing, Gastric cancer, Gastroesophageal reflux disease, Hallucinations, Neurosensory hearing impairment, Hearing loss, High palate, Hirschsprung disease, Hydrocephalus, Hypoplasia of the maxilla, Hypoplasia of the optic nerve, Hypospadias, Imperforate anus, Mental retardation, Lujan-fryns syndrome, Lung carcinoma, Macrocephaly, Macrostomia, Cystosarcoma phyllodes, Malrotation of colon, Marfan syndrome, Meckel diverticulum, Mental depression, Mental retardation, x-linked, Micrognathism, Microstomia, Microtia, Mitral valve prolapse, Mood swings, Motor delay, Multiple congenital anomalies, Hypotonia, Neuronal heterotopia, Non-syndromic intellectual disability, x-linked, Nonorganic psychosis, Obesity, Obsessive-compulsive disorder, Ohdo syndrome, x-linked, Pancreatic adenocarcinoma, Partial agenesis of corpus callosum, Phyllodes tumor, Pierre-robin syndrome, Plagiocephaly, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Psychosis, Ptosis, Pulmonary arterial hypertension, Schizophrenia, Scoliosis, Seizure, Social communication disorder, Speech disorders, Stenosis of external auditory canal, Strabismus, Submucosal cleft palate, Syndactyly, Syndactyly of fingers, Syndactyly of the toes, Thoracic aortic aneurysm and aortic dissection, Urogenital abnormalities, Ventricular septal defectView all (78 more) |
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12213
|
|
|
Mediator complex subunit 13 |
ARC250, DRIP250, HSPC221, MRD61, THRAP1, TRAP240 |
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12214
|
|
|
Nuclear receptor subfamily 1 group I member 3 |
CAR, CAR1, MB67 |
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12215
|
|
|
Nuclear receptor subfamily 1 group H member 4 |
BAR, FXR, HRR-1, HRR1, PFIC5, RIP14 |
Atherosclerosis, Cholestasis, Cholestasis of pregnancy, Ciliopathies, Cirrhosis, Crohn disease, Crohn`s disease of large bowel, Crohn`s disease of the ileum, Fatty liver, Fibroatheroma, Hypoglycemia, Ileocolitis, Intestinal neoplasms, Intestinal cancer, Intrahepatic cholestasis, Intrahepatic cholestasis of pregnancy, Liver neoplasms, Liver cancer, Liver carcinoma, Liver failure, Non-alcoholic fatty liver diseaseView all (6 more) |
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12216
|
|
|
Nucleoporin 153 |
HNUP153, N153 |
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|
12217
|
|
|
Copper chaperone for superoxide dismutase |
- |
|
|
12218
|
|
|
Nuclear receptor subfamily 1 group D member 2 |
BD73, EAR-1R, REVERBB, REVERBbeta, RVR |
|
|
12219
|
|
|
Ring-box 1 |
BA554C12.1, RNF75, ROC1 |
|
|
12220
|
|
|
Cell division cycle 42 |
CDC42Hs, G25K, TKS |
Adrenal cancer, Adrenal neoplasia, Anaplastic carcinoma, Carcinoma, Cerebellar atrophy, Cerebellar hypoplasia, Cerebral cortical atrophy, Clinodactyly, Congenital camptodactyly, Cryptorchidism, Developmental delay, Dysmorphic features, Endometriosis, Exotropia, Hearing loss, Heart septal defects, Hydronephrosis, Hypoplasia of corpus callosum, Hypospadias, Immunologic deficiency syndromes, Macrostomia, Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome, Mental retardation, Multiple congenital anomalies, Neck webbing, Nevus, Oculomotor nerve palsy, Optic atrophy, Patent ductus arteriosus, Platelet-type bleeding disorder, Posteriorly rotated ear, Ptosis, Pulmonary stenosis, Renal aplasia, Schizophrenia, Scoliosis, Strabismus, Synophrys, Takenouchi-kosaki syndrome, Uterine fibroids, Plexiform leiomyomaView all (26 more) |
