|
2311
|
|
|
GNAS antisense RNA 1 |
GNAS-AS, GNAS1AS, GNASAS, NCRNA00075, NESP-AS, NESPAS, SANG |
|
|
2312
|
|
|
Catenin beta 1 |
CTNNB, EVR7, MRD19, NEDSDV, armadillo |
Absent antitragus, Adamantinous craniopharyngioma, Adenocarcinoma, Adenoma, Hyperaldosteronism, Adrenal cancer, Adrenal neoplasia, Adrenocortical adenoma, Adrenocortical carcinoma, Autism, Bicuspid aortic valve, Brain neoplasms, Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Carcinoma of the head and neck, Cardiomyopathy, Cataract, Cecal neoplasm, Cecum cancer, Cerebral palsy, Uterine cervix neoplasm, Cervical cancer, Cirrhosis, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Congenital microcephaly, Craniopharyngioma, Desmoid tumor, Developmental delay, Developmental regression, Diabetes insipidus, Diabetes mellitus, Dysarthria, Dysgerminoma, Dysmorphic features, Dyssomnia, Endometrial cancer, Endometrial neoplasms, Endometrial carcinoma, Esophageal carcinoma, Esophagus neoplasm, Esotropia, Exudative vitreoretinopathy, Fibromatosis, Gastric cancer, Hemangiosarcoma, Hepatoblastoma, Hepatocellular adenoma, Hepatocellular carcinoma, Hereditary nonpolyposis colorectal cancer, High palate, Hydrocephalus, Hydronephrosis, Hyperopia, Hyperopic astigmatism, Hypogonadotropic hypogonadism, Hypoplasia of corpus callosum, Imperforate anus, Mental retardation, Intellectual disability and progressive spastic diplegia, Intestinal neoplasms, Intestinal cancer, Intestinal obstruction, Intestinal polyposis, Left ventricular hypertrophy, Leiomyosarcoma of uterus, Spastic diplegia, Liver neoplasms, Liver carcinoma, Liver cancer, Liver cirrhosis, Liver fibrosis, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Malignant lymphoma, lymphocytic, intermediate differentiation, Lymphoma, lymphocytic, intermediate, Malabsorption syndrome, Malignant mesothelioma, Malignant neoplasm, Malignant uterine corpus neoplasm, Marfan syndrome, Medulloblastoma, Medullomyoblastoma, Melanoma, Microcephaly, Microcystic stromal tumor, Micronodular cirrhosis, Motor delay, Movement disorders, Multiple congenital anomalies, Myocardial infarction, Myocardial ischemia, Myopia, Neoplasms, Nephroblastoma, Neurodevelopmental disorders, Nystagmus, Obesity, Optic atrophy, Oral aversion, Oropharyngeal dysphagia, Ovarian neoplasm, Ovarian cancer, Ovarian carcinoma, Ovarian papillary adenocarcinoma, Pancreatic adenocarcinoma, Pancreatic neoplasm, Pancreatic cancer, Papillary adenoma, Papillary craniopharyngioma, Papilledema, Parathyroid adenoma, Parathyroid neoplasms, Peritoneal neoplasms, Peritoneal carcinomatosis, Pilomatrixoma, Portal vein thrombosis, Primary tethered cord syndrome, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer, Renal carcinoma, Retinal perforations, Salivary gland neoplasm, Schizophrenia, Adrenal insufficiency, Hypothyroidism, Skin neoplasms, Sleep apnea, Sleep disorders, Speech disorders, Stevens-johnson syndrome, Stomach neoplasms, Strabismus, Syringomyelia, Teratoma, Bladder carcinoma, Vitreoretinal degeneration, Wilms tumorView all (128 more) |
|
2313
|
|
|
Lipase I |
CT17, LPDL, PLA1C, PRED5, mPA-PLA1 beta |
|
|
2314
|
|
|
Aralkylamine N-acetyltransferase |
DSPS, SNAT |
|
|
2315
|
|
|
Adrenoceptor alpha 2A |
ADRA2, ADRA2R, ADRAR, ALPHA2AAR, FPLD8, ZNF32 |
|
|
2316
|
|
|
Catenin delta 1 |
BCDS2, CAS, CTNND, P120CAS, P120CTN, p120, p120(CAS), p120(CTN) |
|
|
2317
|
|
|
ATP binding cassette subfamily C member 13 (pseudogene) |
ABCC13P, C21orf73, PRED6 |
|
|
2318
|
|
|
Immunoglobulin superfamily member 5 |
GSF5, JAM4 |
|
|
2319
|
|
|
Salt inducible kinase 1 |
DEE30, MSK, SIK, SIK-1, SIK1B, SNF1LK |
Arthritis, Autism, Cardiomyopathy, Cerebellar atrophy, Choreoathetosis, Clonic seizures, Congenital exomphalos, Developmental delay, Developmental regression, Dyskinetic syndrome, Dysphagia, Dyssomnia, Eczema, Epileptic encephalopathy, Episodic ataxia, Eyelid myoclonias, Febrile seizures, Focal seizures, Focal tonic seizures, Glioblastoma, Hypoplasia of corpus callosum, Hypotonic seizures, Juvenile arthritis, Mental retardation, Metastatic melanoma, Microcephaly, Myoclonic encephalopathy, Myoclonic seizures, Pachygyria, Penis agenesis, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Precocious puberty, Renal dysplasia, Seizure, Sleep disorders, Spasms syndrome, Spasms x-linked, Stereotyped behavior, Still disease, Strabismus, Ureterocele, Ventricular septal defect, West syndromeView all (29 more) |
|
2320
|
|
|
Catenin delta 2 |
GT24, NPRAP |
5p partial monosomy syndrome, Amyotrophic lateral sclerosis, Autism, Benign myoclonic epilepsy, Colorectal cancer, Congenital epicanthus, Dwarfism, Giant cell glioblastoma, Glioblastoma, High palate, Mental retardation, Lateral sclerosis, Mental depression, Microcephaly, Monosomy 5p, Movement disorders, Myoclonic epilepsy, Narcolepsy, Schizophrenia, Scoliosis, Seizure, Syndactyly of fingersView all (7 more) |
