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
3131 to 3140 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

3131
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

3132
Cathepsin E
CATE
Liver cirrhosis

3133
Cathepsin F
CATSF, CLN13
Neuronal ceroid lipofuscinosis, Bipolar disorder, Breast cancer, Developmental disability, Neurodevelopmental disorder

3134
Cathepsin G
CATG, CG
Congenital heart disease, Conotruncal cardiac defect

3135
Cathepsin H
ACC-4, ACC-5, ACC4, ACC5, CPSB
Alzheimer disease, Autoimmune disease, Basal cell carcinoma, Bipolar disorder, Celiac disease, Diabetes mellitus type 1, Gastroesophageal reflux disease, Keratinocyte carcinoma, Myeloid leukemia, Multiple sclerosis, Narcolepsy, Diabetes mellitus type 2

3136
Cathepsin K
CTS02, CTSO, CTSO1, CTSO2, PKND, PYCD
Atrial fibrillation, Dental enamel hypoplasia, Desbuquois syndrome, Glioblastoma, Non-melanoma skin carcinoma, Osteoarthritis, Periodontitis, Prostate cancer, Schizophrenia, Scoliosis, Skeletal dysplasia, Squamous cell carcinoma

3137
Cathepsin L
CATL, CTSL1, MEP
Hypertrophic cardiomyopathy, Meningioma, Proteinuria, Stomach neoplasms

3138
Cathepsin S
-
Atrial fibrillation, Basal cell carcinoma, Contact dermatitis, Coronary artery disease, Melanoma, Cutaneous squamous cell carcinoma, Liver cirrhosis, Multiple sclerosis, Neuropathy, Non-melanoma skin carcinoma, Obesity, Paroxysmal tachycardia, Squamous cell carcinoma

3139
Cathepsin V
CATL2, CTSL2, CTSU
Lewy body disease, Scoliosis

3140
Cathepsin W
LYPN
Hyperuricemia