Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "C"
1641 to 1650 of 1806 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

1641
Cathepsin E
CATE
Liver cirrhosis

1642
Cathepsin F
CATSF, CLN13
Neuronal ceroid lipofuscinosis, Bipolar disorder, Breast cancer, Developmental disability, Neurodevelopmental disorder

1643
Cathepsin G
CATG, CG
Congenital heart disease, Conotruncal cardiac defect

1644
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 1, Diabetes mellitus, type 2

1645
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

1646
Cathepsin L
CATL, CTSL1, MEP
Hypertrophic cardiomyopathy, Meningioma, Proteinuria, Stomach neoplasms

1647
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

1648
Cathepsin V
CATL2, CTSL2, CTSU
Lewy body disease, Scoliosis

1649
Cathepsin W
LYPN
Hyperuricemia

1650
Cathepsin Z
CTSX
Myeloid leukemia, Liver cirrhosis, Meniere disease