821
|
|
|
Coiled-coil and C2 domain containing 1A |
Aki-1, FREUD-1, Freud-1/Aki1, Lgd2, MRT3, TAPE |
Absence of septum pellucidum, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Non-syndromic intellectual disability, Polymicrogyria, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (4 more) |
822
|
|
|
Centlein |
C9orf101, C9orf39, bA340N12.1 |
|
823
|
|
|
Castor zinc finger 1 |
CAS11, CST, SRG, ZNF693, dJ734G22.1 |
Alopecia, Atrial fibrillation, Breast carcinoma, Cardiovascular diseases, Chronic obstructive pulmonary disease, Hypertension, Ischemic stroke, Paroxysmal atrial fibrillation, Prostatic neoplasms, Prostate cancer, Stroke, Vulval varices |
824
|
|
|
CDKAL1 threonylcarbamoyladenosine tRNA methylthiotransferase |
- |
Alzheimer disease, Ankylosing spondylitis, Asthma, Autism, Urinary bladder cancer, Bladder carcinoma, Breast carcinoma, Cardiovascular diseases, Cholangitis, Coronary heart disease, Crohn disease, Diabetes mellitus, Inflammatory bowel disease, Malignant melanoma of skin, Melanoma, Multiple sclerosis, Narcolepsy, Psoriasis, Psoriasis vulgaris, Stroke, Synovitis, acne, pustulosis, hyperostosis, and osteitis (sapho) syndrome, Ulcerative colitisView all (7 more) |
825
|
|
|
Chromosome 2 open reading frame 42 |
- |
|
826
|
|
|
CLN6 transmembrane ER protein |
CLN4A, CLN6A, HsT18960, nclf |
Action myoclonus-renal failure syndrome, Cerebral atrophy, Dementia, Dentatorubral pallidoluysian atrophy, Developmental dyspraxia, Developmental regression, Disorder of eye, Hemeralopia, Inclusion-body disease, Leukoencephalopathy, May-white syndrome, Mental depression, Motor skills disorders, Myoclonic epilepsy, Neuronal ceroid lipofuscinosis, Vision disabilityView all (1 more) |
827
|
|
|
Coiled-coil domain 40 molecular ruler complex subunit |
CFAP172, CILD15, FAP172 |
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Ciliopathies, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Kartagener syndrome, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (4 more) |
828
|
|
|
Cartilage acidic protein 1 |
ASPIC, ASPIC1, CEP-68, CEP68, LOTUS |
|
829
|
|
|
Centrosomal protein 192 |
PPP1R62 |
|
830
|
|
|
Cell division cycle associated 8 |
BOR, BOREALIN, DasraB, MESRGP |
|