6351
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|
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Cut like homeobox 2 |
CDP2, CUTL2, DEE67, EIEE67 |
Curated: Alzheimer disease, Atrial fibrillation, Bipolar disorder, Breast cancer, Cardiac arrhythmia, Kidney disease, Color vision deficiency, Colorectal cancer, Coronary artery disease, Developmental and epileptic encephalopathy, Epilepsy, Esophageal cancer, Esophageal disease, Gastric cancer, Gastresophageal reflux disease, Generalized epilepsy, Gout, Hypertension, Osteonecrosis of the femoral head, Kidney failure, Lennox-gastaut syndrome, Major depressive disorder, Myocardial infarction, Partial epilepsy, Polycystic ovary syndrome, Diabetes mellitus type 1, Diabetes mellitus type 2, Venous thromboembolism, Genetic developmental and epileptic encephalopathy, Seizures, Intellectual disability, Autistic behavior
Unreviewed: Absence epilepsy, Absence Seizure, Atrial Fibrillation, Autism, Autism spectrum disorder, Bipolar Disorder, Brain disease, Breast neoplasm, Cognition disorder, Coronary Heart Disease, Cortical Dysplasia, Crohn disease, Developmental Delay, Diabetes Mellitus, Diabetes mellitus, type 1, Diabetes mellitus, type 2, Dyskinetic Syndrome, Epileptic encephalopathy, Gouty arthritis, Hypotonic seizures, Intellectual developmental disorder, Lennox-Gastaut Syndrome, Major Affective Disorder, Mental retardation, Multiple Sclerosis, Myoclonic epilepsy, Myoclonic Seizures, Neurodevelopmental Disorders, Papillary thyroid carcinoma, Personality Disorders, Rosacea, Schizophrenia, Seizure, Stomach Carcinoma, Stomach neoplasms
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6352
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|
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Cut like homeobox 2 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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6353
|
|
|
Cut like homeobox 2 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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6354
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|
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CUB and zona pellucida like domains 1 |
ERG-1, ERG1, ITMAP1, UO-44 |
Curated: Schizophrenia
Unreviewed: Crohn Disease, Esophagus Neoplasm, Inflammatory Bowel Disease, Long QT Syndrome, Malignant Neoplasm, Mammary Neoplasms, Neoplasms, Pancreatitis, Prostate cancer, Sclerosing Cholangitis, Syndromic microphthalmia, Ulcerative colitis
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6355
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|
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- |
- |
Curated: N/A
Unreviewed: N/A
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6356
|
|
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CWC15 spliceosome associated protein |
AD002, C11orf5, Cwf15, HSPC148, ORF5 |
Curated: Attention deficit hyperactivity disorder, Conduct disorder, Scoliosis
Unreviewed: Myxoma, Respiration Disorders, Respiratory Tract Diseases, Vitiligo
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6357
|
|
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CWC22 spliceosome associated protein |
EIF4GL, NCM, fSAPb |
Curated: Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Colorectal cancer, Essential tremor, Female infertility, Gout, Major depressive disorder, Metabolic syndrome, Obesity, Ovarian cancer, Pelvic organ prolapse, Prostate cancer, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2, Uterine cancer
Unreviewed: Amyotrophic lateral sclerosis, Colitis, Colorectal neoplasm, Neoplasms, Parkinson disease, Polyneuropathy
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6358
|
|
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CWC25 spliceosome associated protein |
CCDC49 |
Curated: Alzheimer disease, Major depressive disorder
Unreviewed: N/A
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6359
|
|
|
CWC27 spliceosome associated cyclophilin |
NY-CO-10, RPSKA, SDCCAG-10, SDCCAG10 |
Curated: Brachydactyly-short stature-retinits pigmentosa syndrome, Central nervous system cancer, Color vision deficiency, Diverticular disease, Diverticulitis, Glioblastoma, Glioma, Heart failure, Metaphyseal chondrodysplasia with retinitis pigmentosa, Obesity, Optic atrophy, Osteoarthritis, Osteonecrosis, Retinitis pigmentosa, Retinitis pigmentosa with or without skeletal anomalies, Schizophrenia, Urinary bladder cancer
Unreviewed: Alzheimer disease, Bladder carcinoma, Bladder Neoplasm, Brachydactyly, Brachydactyly-Short Stature-Retinitis Pigmentosa Syndrome, Cognition disorder, Diverticular Diseases, Dwarfism, Frontal bossing, Macrocephaly, Macrotia, Mental retardation, Metaphyseal Chondrodysplasia, Metaphyseal Chondrodysplasia With Retinitis Pigmentosa, Micrognathism, Mitochondrial disease, Nyctalopia, Retinal degeneration, Retinitis Pigmentosa, Rod-cone dystrophy, Urinary bladder neoplasms
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6360
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|
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CWF19 like cell cycle control factor 1 |
C19L1, SCAR17, hDrn1 |
Curated: Spinocerebellar ataxia, Cerebellar ataxia, Intellectual developmental disorder, Nonalcoholic fatty liver disease, Psoriasis, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm, Autosomal recessive cerebellar ataxia, Developmental delay with epilepsy, progressive ataxia and cerebellar atrophy
Unreviewed: Agenesis Of Corpus Callosum, Ataxia, Atrophy, Cerebellar Ataxia, Cerebellar atrophy, Cerebellar Hypoplasia, Developmental Delay, Diabetes mellitus, type 2, Dysarthria, Fatty Liver, Horizontal nystagmus, Mental retardation, Movement Disorders, Non-Alcoholic Fatty Liver Disease, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Spinocerebellar Ataxia, Synophrys
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