4681
|
|
|
CEP192 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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4682
|
|
|
CEP19 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4683
|
|
|
Centrosomal protein 20 |
C16orf63, FOPNL, FOR20, PHSECRG2 |
Curated: Multiple myeloma, Pelvic organ prolapse, Psoriasis
Unreviewed: Ciliopathies, Diabetes, Diabetes Mellitus, Endometrial Cancer, Endometrial carcinoma, Hypertension, Ischemic Stroke, Liver carcinoma, Merkel cell carcinoma, Orofaciodigital syndrome, Skin carcinoma, Stroke
|
4684
|
|
|
Centrosomal protein 250 |
C-NAP1, CEP2, CNAP1, CRDHL2 |
Curated: Cone rod dystrophy and hearing loss, Optic atrophy, Retinitis pigmentosa, Usher syndrome
Unreviewed: Cone-rod dystrophy, Hearing Loss, Hepatocellular carcinoma, Hypoalphalipoproteinemia, Lymphoma, Malignant Neoplasm, Nasopharyngeal carcinoma, Pancreatic neoplasm, Retinal detachment, Retinitis Pigmentosa, Rod-cone dystrophy, Usher Syndrome, Visual disorder
|
4685
|
|
|
CEP250 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
4686
|
|
|
Centrosomal protein 290 |
3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16 |
Curated: Arima syndrome, Hemolytic uremic syndrome, Bardet-biedl syndrome, Blindness, Cone-rod dystrophy, Congenital kidney anomaly, Congenital disorder of glycosylation, Congenital neurologic anomalies, Cystic kidney disease, Desbuquois syndrome, Encephalocele, Aplasia of the vermis, Global developmental delay, Intellectual developmental disorder, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Meckel-gruber syndrome, Micrognathism, Nephronophthisis, Nystagmus, Optic atrophy, Polycystic kidney disease, Retinitis pigmentosa, Rod-cone dystrophy, Senior-loken syndrome, Spastic ataxia, Stuve-wiedemann syndrome, CEP290-related ciliopathy
Unreviewed: Alstrom Syndrome, Anencephaly, Arima Syndrome, Asplenia, Atrial Septal Defect, Atrioventricular septal defect, Autism, Bardet-Biedl Syndrome, Cataract, Cerebellar vermis agenesis, Choroideremia, Ciliopathies, Ciliopathy, Color vision deficiency, Cone dystrophy, Congenital blindness, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Congenital Hypoplasia Of Penis, Congenital Meningocele, Congenital nystagmus, Congenital ocular coloboma, Congestive Heart Failure, Cryptorchidism, Cystic Kidney Disease, Cystic liver disease, Dandy-Walker Syndrome, Developmental Delay, Developmental disability, Diastrophic Dysplasia, Disorder Of Eye, Double Ureter, Down syndrome, Drachtman Weinblatt Sitarz syndrome, Dwarfism, Fibrosis Of Pancreas, Foot Polydactyly, Fundus Coloboma, Growth disorder, Hemiplegia/hemiparesis, Hemochromatosis, Hepatocellular carcinoma, Hereditary Leber Optic Atrophy, Hirschsprung Disease, Hydrocephalus, Hypertension, Hypogonadism, Hypogonadotropic hypogonadism, Hypoplasia Of Corpus Callosum, Hypoplasia of the ovary, Joubert Syndrome, Joubert Syndrome With Oculorenal Defect, Kallmann syndrome, Keratoconus, Keratosis Follicularis, Kidney Disease, Leber Congenital Amaurosis, Liver Fibrosis, Lobar Holoprosencephaly, Macular dystrophy, Male Pseudohermaphroditism, Malformation of cortical development, Meckel Syndrome, Meckel-Gruber Syndrome, Mental retardation, Microcephaly, Microcornea, Microphthalmos, MOHR-TRANEBJAERG SYNDROME, Multicystic renal dysplasia, Nephrotic Syndrome, Obesity, Occipital Encephalocele, Oculocerebrorenal syndrome, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Optic Atrophy, Orofaciodigital syndrome, Pancreatic Cyst, Polycystic liver disease, Polydactyly, Polydactyly Of Toes, Postaxial hand polydactyly, Premature Menopause, Ptosis, Renal cyst, Renal dysplasia and retinal aplasia, Renal Insufficiency, Retinal coloboma, Retinal degeneration, Retinal detachment, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Sclerocornea, Scoliosis, Senior-Loken Syndrome, Situs Inversus, Sleep Apnea, Speech Disorders, Strabismus, Syndactyly of fingers, Syndromic microphthalmia, Talipes, Trichohepatoenteric Syndrome, True Hermaphroditism, Urethral atresia, Ventricular septal defect, Visual disorder
|
4687
|
|
|
Centrosomal protein 295 |
KIAA1731, SCKL11 |
Curated: Bell's palsy, Central nervous system cancer, Glioblastoma, Glioma, Meckel-gruber syndrome, Neuroblastoma, Scoliosis, Seckel syndrome
Unreviewed: Ciliary dyskinesia, Ciliopathy, Craniofacial abnormalities, Developmental disability, Glaucoma, Growth disorder, Intellectual developmental disorder, Microcephaly, Primary microcephaly
|
4688
|
|
|
CEP295 N-terminal like |
DDC8, KIAA1731NL |
Curated: Eosinophilia, Alzheimer disease, Respiratory system disease
Unreviewed: Dupuytren Contracture, Respiratory Tract Diseases
|
4689
|
|
|
Centrosomal protein 350 |
CAP350, GM133 |
Curated: Kidney cancer, Kidney neoplasms, Prostate cancer
Unreviewed: Chronic obstructive pulmonary disease, Ciliopathies, Dysbiosis, Glioblastoma, Hepatitis c, Liver failure, Melanoma, Mesothelioma, Neoplasms, Obesity
|
4690
|
|
|
Centrosomal protein 41 |
JBTS15, TSGA14 |
Curated: Autism, Obstructive pulmonary disease, Aplasia of the vermis, Joubert syndrome, Retinitis pigmentosa, Venous thromboembolism, ciliopathy
Unreviewed: Agenesis Of Corpus Callosum, Autism Spectrum Disorder, Cerebellar vermis agenesis, Ciliopathies, Colorectal neoplasm, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Connective tissue disease, Developmental Delay, Dextrocardia, Disorder Of Eye, Ewing sarcoma, Eye disease, Fundus Coloboma, Hirschsprung Disease, Hydrocephalus, Joubert Syndrome, Joubert Syndrome With Ocular Defect, Joubert syndrome, Digenic, Mental retardation, Neoplasms, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oral cleft, Penis Agenesis, Polydactyly, Polydactyly Of Toes, Polymicrogyria, Ptosis, Retinal coloboma, Retinal Dystrophy, Sarcoma, Schizophrenia, Scoliosis, Situs Inversus, Strabismus
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