|
671
|
|
|
CTBP1 antisense RNA |
PCAT10 |
|
|
672
|
|
|
Crumbs cell polarity complex component 2 |
FSGS9, VMCKD |
Astrocytoma, Central nervous system cancer, Cystic kidney disease with ventriculomegaly, Dementia, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Focal segmental glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glioblastoma, Glioma, Hereditary steroid-resistant nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, focal segmental type, Oligodendroglioma, Retinitis pigmentosa, Steroid-resistant nephrotic syndrome, Thyroid cancer, Diabetes mellitus, type 2, Ventriculomegaly with cystic kidney diseaseView all (4 more) |
|
673
|
|
|
CCC complex scaffolding subunit CCDC22 |
CXorf37, JM1, RTSC2 |
|
|
674
|
|
|
Cytochrome c oxidase assembly factor 3 |
CCDC56, COX25, HSPC009, MC4DN14, MITRAC12, hCOA3 |
|
|
675
|
|
|
C1GALT1 specific chaperone 1 |
AHUS8, C1GALT2, C38H2-L1, COSMC, HSPC067, MST143, TNPS |
|
|
676
|
|
|
Coiled-coil domain containing 59 |
BR22, HSPC128, TAP26 |
|
|
677
|
|
|
Chromosome 6 open reading frame 15 |
STG |
Autoimmune neurological syndrome, Autism, Behcet disease, Celiac disease, Colorectal cancer, Crohn disease, Graves disease, Immune system disease, Inflammatory bowel disease, Leprosy, Lung cancer, Major depressive disorder, Membranous glomerulonephritis, Myasthenia gravis, Nasopharyngeal carcinoma, Neurotic disorder, Peripheral arterial disease, Prostate cancer, Psoriasis, Raynaud disease, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Small cell lung carcinoma, Squamous cell carcinoma, Thyrotoxic periodic paralysis, Diabetes mellitus, type 1, Ulcerative colitisView all (13 more) |
|
678
|
|
|
Catenin alpha 3 |
ARVD13, VR22 |
Alzheimer disease, Arrhythmogenic right ventricular cardiomyopathy, Asthma, Astrocytoma, Atrial fibrillation, Attention deficit hyperactivity disorder, Brain aneurysm, Brain compression, Breast cancer, Bronchopulmonary dysplasia, Dilated cardiomyopathy, Cardiomyopathy, Central nervous system cancer, Congenital heart disease, Dental caries, Edema, Esophageal disease, Essential tremor, Arrhythmogenic right ventricular dysplasia, Glioblastoma, Glioma, Hypertension, Iga nephropathy, Insomnia, Interstitial lung disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome, Major depressive disorder, Migraine, Intellectual disability, Neurotic disorder, Obesity, Peripheral neuropathy, Psoriatic arthritis, Psychiatric disorders, Willis-ekbom disease, Rheumatic heart disease, Schizophrenia, Scoliosis, Substance abuse, Systemic lupus erythematosus, Thoracic aortic aneurysm, Ulcerative colitisView all (28 more) |
|
679
|
|
|
C-type lectin domain family 2 member D |
CLAX, LLT1, OCIL |
|
|
680
|
|
|
Chromosome 11 open reading frame 21 |
- |
|
