|
1081
|
|
|
Calreticulin |
CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR |
Anemia, Anorexia, Bipolar disorder, Colorectal cancer, Colorectal neoplasms, Esophagus neoplasm, Hemangioma, Hematologic neoplasms, Hypertension, Leukemia, Myelodysplasia, Myelodysplastic syndrome, Myelofibrosis, Myeloproliferative disorder, Myocardial infarction, Myocardial ischemia, Nonorganic psychosis, Pancytopenia, Paranoid schizophrenia, Portal hypertension, Prostatic neoplasms, Prostate cancer, Psychosis, Schizoaffective disorder, Shared paranoid disorder, Thrombocythemia, Thrombocytosis, Transient ischemic attackView all (13 more) |
|
1082
|
|
|
Calumenin |
- |
|
|
1083
|
|
|
Calcium/calmodulin dependent protein kinase IV |
CaMK IV, CaMK-GR, CaMKIV, caMK |
|
|
1084
|
|
|
Complement factor H related 5 |
CFHL5, CFHR5D, FHR-5, FHR5 |
Breast cancer, C3 glomerulonephritis, C3 glomerulopathy, Cholestasis, Complement component deficiency, Exudative macular degeneration, Geographic atrophy, Glomerulonephritis, Hemolytic uremic syndrome, Kidney disease, Kidney failure, Age-related macular degeneration |
|
1085
|
|
|
Calcium/calmodulin dependent protein kinase II alpha |
CAMKA, CaMKIINalpha, CaMKIIalpha, MRD53, MRT63 |
Bipolar disorder, Congenital digestive system anomalies, Congenital epicanthus, Developmental delay, Hepatolenticular degeneration, Inflammatory bowel disease, Mental retardation, Mental depression, Movement disorders, Myoclonic seizures, Non-syndromic intellectual disability, Strabismus, Ulcerative colitis, Urogenital abnormalities, Ventricular septal defect |
|
1086
|
|
|
Chromosome 1 open reading frame 21 |
PIG13 |
|
|
1087
|
|
|
ClpB family mitochondrial disaggregase |
ANKCLB, ANKCLP, HSP78, MEGCANN, MGCA7, MGCA7A, SCN9, SKD3 |
Anxiety disorder, Cardiomyopathy, Cataract, Cerebellar atrophy, Cerebral atrophy, Choreoathetosis, Clinodactyly, Congenital microcephaly, Developmental delay, Developmental regression, Ectodermal dysplasia, Epilepsy, Epileptic encephalopathy, Fatty liver, Hypothyroidism, Mental retardation, Microcephaly, Multiple congenital anomalies, Hypoglycemia, Hypotonia, Nephrocalcinosis, Neutropenia, Nystagmus, Renal cyst, Renal insufficiency, Respiratory failure, Postaxial hand polydactylyView all (12 more) |
|
1088
|
|
|
Collagen type XXI alpha 1 chain |
COLA1L, FP633 |
|
|
1089
|
|
|
Calcium/calmodulin dependent protein kinase II beta |
CAM2, CAMK2, CAMKB, CaMKIIbeta, MRD54 |
Arthritis, Colorectal cancer, Congenital digestive system anomalies, Developmental delay, Dyskinetic syndrome, Gastroesophageal reflux disease, Intracranial aneurysm, Mental retardation, Metabolic syndrome, Movement disorders, Non-syndromic intellectual disability, Schizophrenia, Strabismus |
|
1090
|
|
|
Calcium binding protein 39 like |
MLAA-34, MO25-BETA, MO2L, bA103J18.3 |
|
