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
3111 to 3120 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3111
Chymotrypsinogen B1
CTRB
Coronary artery disease, Diabetes mellitus, Hypoxia, Metabolic syndrome, Pancreatic cancer, Diabetes mellitus type 1, Diabetes mellitus type 2

3112
Chymotrypsinogen B2
-
Atrophic macular degeneration, Coronary artery disease, Diabetes mellitus, Diabetic neuropathy, Metabolic syndrome, Pancreatic cancer, Diabetes mellitus type 1, Diabetes mellitus type 2, Age-related macular degeneration

3113
Chymotrypsin C
CLCR, ELA4
Hereditary chronic pancreatitis, Pancreatitis, Tropical calcific pancreatitis

3114
Chymotrypsin like
CTRL1
Schizophrenia

3115
Cathepsin A
GLB2, GSL, NGBE, PPCA, PPGB
Cathepsin a-related arteriopathy, strokes, and leukoencephalopathy, Combined deficiency of sialidase and beta galactosidase, Desbuquois syndrome, Galactosialidosis, Non-immune hydrops fetalis

3116
Cathepsin B
APPS, CPSB, KWE, RECEUP
Alzheimer disease, Renal cell carcinoma, Diabetes mellitus, Glioblastoma, Irritable bowel syndrome, Metabolic syndrome, Myopathy, Necrosis, Neurotic disorder, Parkinson disease, Prostatic neoplasms, Proteinuria, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

3117
Cathepsin C
CPPI, DPP-I, DPP1, DPPI, HMS, JP, JPD, PALS, PDON1, PLS
Dementia, Allergic contact dermatitis, Ectodermal dysplasia, Myocardial ischemia, Narcolepsy, Papillon-lefevre syndrome, Periodontal disease, Periodontitis, Post-traumatic stress disorder, Stomach neoplasms

3118
Cathepsin D
CLN10, CPSD, HEL-S-130P
Alzheimer disease, Amyotrophic lateral sclerosis, Rheumatoid arthritis, Hepatocellular carcinoma, Renal cell carcinoma, Neuronal ceroid lipofuscinosis, Diabetic neuropathy, Kidney disease, Motor neuron disease, Osteoarthritis, Prostatic neoplasms, Retinitis pigmentosa

3119
Cathepsin F
CATSF, CLN13
Neuronal ceroid lipofuscinosis, Bipolar disorder, Breast cancer, Developmental disability, Neurodevelopmental disorder

3120
Cathepsin G
CATG, CG
Congenital heart disease, Conotruncal cardiac defect