Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
301 to 310 of 320 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

301
Kinetochore localized astrin (SPAG5) binding protein
C15orf23, HSD11, ROCHIS, SKAP, TRAF4AF1
Androgenetic alopecia, Squamous cell carcinoma, Combined immunodeficiency with faciooculoskeletal anomalies, Combined immunodeficiency with facio-oculo-skeletal anomalies, Roifman syndrome, Secondary malignant neoplasm

302
Keratin 75
CK-75, K6HF, K75, KB18, PFB, hK6hf

303
Potassium voltage-gated channel subfamily Q member 4
DFNA2, DFNA2A, KV7.4
Isolated sensorineural deafness, Nonsyndromic hearing loss, Colorectal cancer, Deafness, Hearing impairment, Inflammatory bowel disease, Hearing loss

304
Potassium voltage-gated channel modifier subfamily G member 4
KV6.3, KV6.4
Alzheimer disease, Scoliosis

305
Potassium voltage-gated channel subfamily B member 2
KV2.2
Brain infarction, Cerebral amyloid angiopathy, Color vision deficiency, Colorectal cancer, Coronary artery disease, Dementia, Gastroesophageal reflux disease, Insomnia, Lewy body disease, Major depressive disorder, Metabolic syndrome, Multiple sclerosis, Neurodevelopmental disorders, Peptic ulcer disease, Post-traumatic stress disorder
View all (5 more)

306
KLF transcription factor 4
EZF, GKLF
Juvenile arthritis, Breast cancer, Chagas cardiomyopathy, Congenital anomalies, Congenital heart defects, Congenital heart defect, Juvenile idiopathic arthritis, Myocardial ischemia, Oligoarticular juvenile idiopathic arthritis, Prostate cancer

307
Klotho
HFTC3, KLA
Arteriosclerosis, Calcinosis, Cerebral embolism, Ischemic heart disease, Coronary artery disease, Dermatologic disorder, Desbuquois syndrome, Diabetes mellitus, Diabetes mellitus type 2, Diabetic neuropathy, Emphysema, Hyperphosphatemic tumoral calcinosis, Hypercalcemia, Infantile hypercalcemia, Hypercalcemic tumoral calcinosis
View all (12 more)

308
Kinesin family member 23
CDA3, CDAIII, CDAN3, CDAN3A, CHO1, KNSL5, MKLP-1, MKLP1
Congenital dyserythropoietic anemia, Hepatocellular carcinoma

309
Kallikrein related peptidase 4
AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17, PSTS, kallikrein
Amelogenesis imperfecta, Atrophic gastritis, Dentin dysplasia, Dentinogenesis imperfecta, Hypomaturation amelogenesis imperfecta, Male infertility, Obesity

310
KIAA0040
-
Astrocytoma, Atrial fibrillation, Central nervous system cancer, Coronary artery disease, Glioblastoma, Glioma, Migraine, Schizophrenia