|
851
|
|
|
Cryptic, EGF-CFC family member 1 |
CFC1B, CRYPTIC, DTGA2, HTX2 |
|
|
852
|
|
|
Cytotoxic and regulatory T cell molecule |
CD355 |
|
|
853
|
|
|
Catenin beta like 1 |
C20orf33, IMD99, NAP, P14L, PP8304, dJ633O20.1 |
|
|
854
|
|
|
C-C motif chemokine ligand 28 |
CCK1, MEC, SCYA28 |
|
|
855
|
|
|
Cytochrome P450 family 26 subfamily B member 1 |
CYP26A2, P450RAI-2, P450RAI2, RHFCA |
|
|
856
|
|
|
Cilia and flagella associated protein 298 |
C21orf48, C21orf59, CILD26, DNAAF16, FBB18, Kur |
|
|
857
|
|
|
CUGBP Elav-like family member 4 |
BRUNOL4, CELF-4 |
Alzheimer disease, Anxiety disorder, Attention deficit hyperactivity disorder, Breast cancer, Obstructive pulmonary disease, Color vision deficiency, Neurodevelopmental disorder, Dementia, Developmental disability, Diverticulitis, Gastroesophageal reflux disease, Irritable bowel syndrome, Major depressive disorder, Intellectual developmental disorder, Migraine, Mood disorder, Neurodevelopmental disorders, Neurotic disorder, Non-specific syndromic intellectual disability, Obesity, Schizophrenia, Diabetes mellitus, type 2View all (7 more) |
|
858
|
|
|
Core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 |
C1GALT, T-synthase |
Alzheimer disease, Cardiovascular disease, Obstructive pulmonary disease, Coronary artery disease, Dementia, Hypertension, Insomnia, Metabolic syndrome, Migraine, Multiple sclerosis, Myocardial infarction, Diabetes mellitus, type 2 |
|
859
|
|
|
Carbonic anhydrase 10 |
CA-RPX, CARPX, HUCEP-15 |
Asthma, Attention deficit hyperactivity disorder, Autism, Obstructive pulmonary disease, Color vision deficiency, Dementia, Gastritis, Gastroesophageal reflux disease, Insomnia, Lung cancer, Myocardial infarction, Peptic ulcer disease, Willis-ekbom disease, Scoliosis, Substance abuse, Diabetes mellitus, type 2View all (1 more) |
|
860
|
|
|
C-X9-C motif containing 2 |
2310061C15Rik, C16orf61, DC13 |
|
