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 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1831
Caveolin 3
LGMD1C, LQT9, MPDT, RMD2, VIP-21, VIP21
Limb girdle muscular dystrophy, Brugada syndrome, Cardiomegaly, Cardiomyopathy, Caveolinopathy, Chromosome 3p25 monosomy, Color vision deficiency, Congenital heart defects, Creatine phosphokinase elevation, Experimental diabetes, Distal myopathy, Long qt syndrome, Congenital heart defect, Hypertrophic cardiomyopathy, Joubert syndrome
View all (3 more)

1832
Caveolae associated protein 1
CAVIN, CGL4, FKSG13, PTRF, cavin-1
Eczema, Berardinelli-seip congenital lipodystrophy, Breast cancer, Congenital generalized lipodystrophy, Coronary artery disease, Crohn disease, Generalized lipodystrophy, Iga nephropathy, Inflammatory bowel disease, Lipodystrophy, Methylmalonic acidemia, Myocardial infarction, Psoriasis, Diabetes mellitus type 2

1833
Caveolae associated protein 2
PS-p68, SDPR, SDR, cavin-2
Hirschsprung disease, Osteoarthritis, Parkinson disease

1834
Caveolae associated protein 3
HSRBC, PRKCDBP, SRBC, cavin-3
Asthma, Insomnia, Ocular sarcoidosis, Willis-ekbom disease, Rheumatic heart disease, Smooth surface dental caries

1835
Caveolae associated protein 4
MURC, cavin-4
Atrial fibrillation, Dilated cardiomyopathy, Scoliosis

1836
CACN subunit beta associated regulatory protein
BARP, C19orf26, DOS
Androgenetic alopecia, Diabetes mellitus type 2

1837
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

1838
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

1839
Core-binding factor subunit beta
CLCD2, PEBP2B
Myeloid leukemia, Androgenetic alopecia, Bone disease, Cleft palate, Cleidocranial dysplasia, Congenital heart defects, Congenital heart defect

1840
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