Genesⓘ

Dataset:
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
301 to 310 of 320 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

301
Kinetochore localized astrin (SPAG5) binding protein
C15orf23, HSD11, ROCHIS, SKAP, TRAF4AF1
Carcinoma, Melanoma, Roifman-chitayat syndrome, Skin carcinoma

302
Keratin 75
CK-75, K6HF, K75, KB18, PFB, hK6hf
Loose anagen hair syndrome

303
Potassium voltage-gated channel subfamily Q member 4
DFNA2, DFNA2A, KV7.4
Deafness, Non-syndromic sensorineural deafness, Nonsyndromic deafness

304
Potassium voltage-gated channel modifier subfamily G member 4
KV6.3, KV6.4
Chronic obstructive pulmonary disease

305
Potassium voltage-gated channel subfamily B member 2
KV2.2
Colorectal cancer, Leukemia

306
KLF transcription factor 4
EZF, GKLF
Arthritis, Congenital heart defects, Juvenile arthritis, Meningioma, Myocardial ischemia, Seronegative polyarthritis, Polyarthritis, rheumatoid factor positive, Still disease

307
Klotho
HFTC3, KLA
Arteriosclerosis, Colorectal cancer, Coronary arteriosclerosis, Coronary artery disease, Dermatologic disorders, Diabetes mellitus, Hypercalcemia, Hypercalciuria, Hyperphosphatemia, Hyperphosphatemic tumoral calcinosis, Kidney disease, Learning disorders, Memory disorders, Age-related memory disorders, Milk-alkali syndrome
View all (4 more)

308
Kinesin family member 23
CDA3, CDAIII, CDAN3, CDAN3A, CHO1, KNSL5, MKLP-1, MKLP1
Anemia, Congenital dyserythropoietic anemia, Dwarfism, Enzymopathy, Hyperbilirubinemia, Liver carcinoma

309
Kallikrein related peptidase 4
AI2A1, ARM1, EMSP, EMSP1, KLK-L1, PRSS17, PSTS, kallikrein
Amelogenesis imperfecta, Hypomaturation amelogenesis imperfecta

310
KIAA0040
-
Amyotrophic lateral sclerosis