31
|
|
|
CYP3A7-CYP3A51P readthrough |
CYP3A7, CYP3A7-3AP1, CYP3A7-CYP3AP1, CYP3A7.1L, CYPIIIA7 |
|
32
|
|
|
Ceramide transporter 1 |
CERT, CERTL, COL4A3BP, GPBP, MRD34, NEDHSF, STARD11 |
Atrial fibrillation, Cardiovascular diseases, Central visual impairment, Congenital epicanthus, Coronary heart disease, Developmental delay, Diabetes, Diabetes mellitus, Epilepsy, Heart failure, Lung carcinoma, Malignant neoplasm, Mental retardation, Neurodevelopmental disorders, Seizure, Stereotyped behavior, Stroke, Syndactyly of the toes, SynophrysView all (4 more) |
33
|
|
|
COX10 divergent transcript |
COX10-AS, COX10-AS1, COX10AS |
|
34
|
|
|
Cadherin 11 |
CAD11, CDHOB, ESWS, OB, OSF-4, TBHS2 |
Amelia, Bladder exstrophy, Blepharochalasis, Brachioskeletogenital syndrome, Brachycephaly, Branchioskeletogenital syndrome, Chronic obstructive pulmonary disease, Congenital absent nipple, Congenital exomphalos, Congenital keratoglobus, Congenital pectus excavatum, Craniosynostosis, Cryptorchidism, Dentin dysplasia, Developmental delay, Exodeviation, Hearing loss, High palate, Hypoplasia of the maxilla, Hypospadias, Malocclusion, Mental retardation, Microcephaly, Penis agenesis, Posteriorly rotated ear, Proptosis, Strabismus, Submucosal cleft palate, Synophrys, Upper limb peromeliaView all (15 more) |
35
|
|
|
Chitinase, acidic pseudogene 3 |
- |
|
36
|
|
|
CA3 antisense RNA 1 |
- |
|
37
|
|
|
Cortexin domain containing 2 |
- |
|
38
|
|
|
Cadherin 12 |
CDHB |
|
39
|
|
|
Cadherin 13 |
CDHH, P105 |
Alzheimer disease, Barrett epithelium, Barrett esophagus, Chronic obstructive pulmonary disease, Coronary artery disease, Crohn disease, Erectile dysfunction, Esophagus neoplasm, Hypothyroidism, Leukemia, Liver carcinoma, Lung carcinoma, Lung neoplasms, Lung cancer, Mental depression, Prostatic neoplasms, Prostate cancer, SchizophreniaView all (3 more) |
40
|
|
|
Cadherin 15 |
CDH14, CDH3, CDHM, MCAD, MRD3 |
|