|
161
|
|
|
Cleavage and polyadenylation specific factor 6 |
CFIM, CFIM68, CFIM72, HPBRII-4, HPBRII-7 |
|
|
162
|
|
|
Chromodomain helicase DNA binding protein 2 |
DEE94, EEOC |
Absence seizure, Action myoclonus-renal failure syndrome, Attention deficit hyperactivity disorder, Autism spectrum disorder, Autism, Dentatorubral pallidoluysian atrophy, Developmental delay, Developmental regression, Dysarthria, Dysmorphic features, Epilepsy, Epileptic encephalopathy, Febrile seizures, Hypotonic seizures, Inclusion-body disease, Lennox-gastaut syndrome, May-white syndrome, Mental retardation, Myoclonic astatic epilepsy, Myoclonic epilepsy, Myoclonic seizures, Myoclonic-astatic epilepsy, Neurodevelopmental disorders, Obsessive-compulsive disorder, Photosensitive tonic-clonic seizures, Personality disorders, Seizure, Status epilepticus, Tourette syndromeView all (14 more) |
|
163
|
|
|
Chromodomain helicase DNA binding protein 3 |
Mi-2a, Mi2-ALPHA, SNIBCPS, ZFH |
Apraxia, Astigmatism, Congenital epicanthus, Developmental delay, Dysarthria, Frontal bossing, Hyperopia, Ischemic stroke, Macrocephaly, Mental retardation, Prostatic neoplasms, Prostate cancer, Prostate cancer, hereditary, Sezary syndrome, Snijders blok-campeau syndrome, Stereotyped behavior, Strabismus, StrokeView all (3 more) |
|
164
|
|
|
Chromodomain helicase DNA binding protein 4 |
CHD-4, Mi-2b, Mi2-BETA, SIHIWES |
Ambiguous genitalia, Arnold-chiari malformation, Astigmatism, Autism, Congenital epicanthus, Cryptorchidism, Development disorder, Dwarfism, Dysmorphic features, Endometrial neoplasms, Endometrial carcinoma, Macrocephaly, Mental retardation, Multiple congenital anomalies, Penis agenesis, Ptosis, Renal insufficiency, Schizophrenia, Sifrim-hitz-weiss syndrome, Tetralogy of fallot, Trigonocephaly, Vesicoureteral refluxView all (7 more) |
|
165
|
|
|
Checkpoint kinase 1 |
CHK1, OZEMA21 |
|
|
166
|
|
|
Citron rho-interacting serine/threonine kinase |
CITK, CRIK, MCPH17, STK21 |
Agenesis of corpus callosum, Cerebellar hypoplasia, Congenital heart defects, Developmental delay, Dwarfism, Inflammatory bowel disease, Mental retardation, Macrotia, Microcephaly, Microlissencephaly, Neuronal heterotopia, Pachygyria, Renal agenesis, Renal aplasia, Ulcerative colitis, Vesicoureteral refluxView all (1 more) |
|
167
|
|
|
Centrosomal protein 43 |
FGFR1OP, FOP |
|
|
168
|
|
|
CRYZL2P-SEC16B readthrough |
- |
|
|
169
|
|
|
CD160 molecule |
BY55, NK1, NK28 |
|
|
170
|
|
|
CLK4 associating serine/arginine rich protein |
CLASP, SFRS16, SWAP2 |
|
