|
131
|
|
|
Chondroitin sulfate proteoglycan 5 |
NGC |
|
|
132
|
|
|
Centrin 1 |
CEN1, CETN |
|
|
133
|
|
|
Claudin 16 |
HOMG3, PCLN1 |
Astigmatism, Hypercalciuria, Hyperopia, Hyperuricemia, Hypomagnesemia, Kidney disease, Medullary nephrocalcinosis, Myopia, Nephrocalcinosis, Nephrolithiasis, Nystagmus, Hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement, Strabismus |
|
134
|
|
|
Chaperonin containing TCP1 subunit 6B |
CCT-zeta-2, CCTZ-2, Cctz2, TCP-1-zeta-2, TSA303 |
|
|
135
|
|
|
Canopy FGF signaling regulator 3 |
CAG4A, DEE60, EIEE60, ERDA5, PRAT4A, TNRC5 |
|
|
136
|
|
|
Corin, serine peptidase |
ATC2, CMH30, CRN, Lrp4, PEE5, TMPRSS10 |
|
|
137
|
|
|
Cholesteryl ester transfer protein |
BPIFF, HDLCQ10 |
Asthma, Atherosclerosis, Cardiovascular diseases, Childhood obesity, Cholesterol-ester transfer protein deficiency, Coronary heart disease, Dyslipidemias, Exudative macular degeneration, Geographic atrophy, Hyperalphalipoproteinemia, Hypercholesterolemia, Hyperlipidemia, Hyperlipoproteinemia, Hypertension, Hypotriglyceridemia, Liver carcinoma, Age-related macular degeneration, Metabolic syndromeView all (3 more) |
|
138
|
|
|
Ceramide synthase 1 |
EPM8, GDF-1, GDF1, LAG1, LASS1, UOG1 |
Action myoclonus-renal failure syndrome, Asplenia, Congenital heart defects, Dementia, Dentatorubral pallidoluysian atrophy, Double outlet right ventricle, Heterotaxia, Inclusion-body disease, May-white syndrome, Mental retardation, Myoclonic epilepsy, Progressive myoclonic epilepsy, Seizure, Tetralogy of fallot, Transposition of great vessels |
|
139
|
|
|
Cofilin 1 |
CFL, HEL-S-15, cofilin |
|
|
140
|
|
|
Cofilin 2 |
NEM7 |
Arthrogryposis multiplex congenita, Atrial fibrillation, Breast cancer, Congenital pectus excavatum, Developmental delay, High palate, Micrognathism, Minicore myopathy with external ophthalmoplegia, Myofibrillar myopathy, Myopathy, Nemaline myopathy, Hypotonia, Paroxysmal atrial fibrillation, Ptosis, Scoliosis |
