Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
1831 to 1840 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1831
CACN subunit beta associated regulatory protein
BARP, C19orf26, DOS
Androgenetic alopecia, Diabetes mellitus type 2

1832
CBFA2/RUNX1 partner transcriptional co-repressor 2
EHT, MTGR1, ZMYND3, p85
Basal cell carcinoma, Benign prostatic hyperplasia, Breast cancer, Cancer, Colorectal cancer, Estrogen-receptor negative breast cancer, Lung cancer, Melanoma, Non-melanoma skin carcinoma, Ovarian cancer, Ovarian serous carcinoma, Prostate cancer, Squamous cell carcinoma, Diabetes mellitus type 2

1833
CBFA2/RUNX1 partner transcriptional co-repressor 3
ETO2, MTG16, MTGR2, RUNX1T3, ZMYND4
Atherosclerosis, Color vision deficiency, Duodenal ulcer, Eye disease, Melanoma, Multiple sclerosis, Neurotic disorder, Non-melanoma skin carcinoma, Oligodendroglioma, Rheumatoid arthritis, Scoliosis, Diabetes mellitus type 1, Diabetes mellitus type 2, Vitiligo

1834
Core-binding factor subunit beta
CLCD2, PEBP2B
Myeloid leukemia, Androgenetic alopecia, Bone disease, Cleft palate, Cleidocranial dysplasia, Congenital heart defects, Congenital heart defect

1835
Cbl proto-oncogene
C-CBL, CBL2, FRA11B, NSLL, RNF55
Congestive heart failure, Cryptorchidism, Desbuquois syndrome, Developmental disability, Early onset vitamin b6 dependent epilepsy, Growth disorder, Heart failure, Male infertility, Myelomonocytic leukemia, Left ventricular noncompaction cardiomyopathy, Neurodevelopmental disorder, Noonan syndrome, Vasculitis

1836
Cbl proto-oncogene B
ADMIO3, Cbl-b, Nbla00127, RNF56
Autoimmune disease, Autoimmune thyroid disease, Bronchopneumonia, Dementia, Diabetes mellitus type 1, Head and neck neoplasm, Hypothyroidism, Multiple sclerosis, Oropharyngeal cancer, Rheumatoid arthritis, Stroke, Upper aerodigestive tract neoplasm, Urticaria

1837
Cbl proto-oncogene C
CBL-3, CBL-SL, RNF57
Alzheimer disease, Crohn disease, Hyperlipidemia

1838
Cobalamin binding intrinsic factor
GIF, IF, IFMH, INF, TCN3
Pernicious anemia, Bipolar disorder, Congenital intrinsic factor deficiency, Schizophrenia

1839
Cerebellin 1 precursor
-
Kidney disease, Kidney failure, Seasonal allergic rhinitis

1840
Cerebellin 2 precursor
-
Alzheimer disease, Angioedema, Biliary atresia, Breast cancer, Calcium metabolism disorders, Cervical cancer, Colorectal cancer, Developmental disorder, Epilepsy, Gastroesophageal reflux disease, Pulmonary hypertension, Metabolic syndrome, Multiple sclerosis, Myopathy, Oligodendroglioma
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