Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6921 to 6930 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6921
Keratin 12
K12, MECD1
Corneal dystrophy, Hereditary corneal dystrophy

6922
Keratin 13
CK13, K13, WSN2
Color vision deficiency, Esophageal squamous cell carcinoma, White spongue nevus

6923
Keratin 14
CK14, EBS1, EBS1A, EBS1B, EBS1C, EBS1D, EBS3, EBS4, K14, NFJ
Epidermolysis bullosa, Epidermolysis bullosa simplex, Breast neoplasms, Squamous cell carcinoma, Dermatopathia pigmentosa reticularis, Esophageal squamous cell carcinoma, Junctional epidermolysis bullosa, Sjogren-larsson syndrome, Tongue neoplasms, Weber-cockayne syndrome

6924
Keratin 15
CK15, K15, K1CO
Adenoid cystic carcinoma, Color vision deficiency, Salivary gland neoplasms

6925
Keratin 16
CK16, FNEPPK, K16, K1CP, KRT16A, NEPPK, PC1
Ectodermal dysplasia, Epidermolytic palmoplantar keratoderma, Pachyonychia congenita, Urinary bladder neoplasms

6926
Keratin 17
39.1, CK-17, K17, PC, PC2, PCHC1
Anonychia, Basal cell carcinoma, Chloracne, Ectodermal dysplasia, Esophageal squamous cell carcinoma, Pachyonychia congenita, Sebocystomatosis, Skin neoplasms

6927
Keratin 18
CK-18, CYK18, K18
Breast neoplasms, Cirrhosis, Liver cirrhosis, Liver failure, Liver neoplasms, Necrosis, Prostate cancer

6928
Keratin 19
CK19, K19, K1CS
Ankylosing spondylitis, Asthma, Autoimmune disease, Cholangitis, Copper overload cirrhosis, Pharyngeal disorder, Esophageal squamous cell carcinoma, Upper respiratory tract disorder

6929
Keratin 2
CK-2e, K2e, KRT2A, KRT2E, KRTE
Colorectal cancer, Contact dermatitis, Ichthyosis, Junctional epidermolysis bullosa, Xeroderma

6930
Keratin 20
CD20, CK-20, CK20, K20, KRT21
Cecal neoplasms, Schizophrenia, Stomach neoplasms