Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
211 to 220 of 320 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

211
KH-type splicing regulatory protein pseudogene 1
-

212
Karyopherin subunit alpha 7
IPOA8, OZEMA17
Alzheimer disease, Ankylosing spondylitis, Asthma, Lymphocytic leukemia, Crohn disease, Epilepsy, Inflammatory bowel disease, Intellectual disability, Oocyte maturation defect, Partial corpus callosum agenesis, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

213
KIT ligand
DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl, MGF, SCF, SF, SHEP7, SLF, WS2F
Isolated sensorineural deafness, Nonsyndromic hearing loss, Carcinoma, Pancreatic carcinoma, Color vision deficiency, Melanoma, Deafness, Kleins syndrome, Myocardial ischemia, Nasal polyp, Obesity, Testicular carcinoma, Waardenburg syndrome

214
Lysine methyltransferase 2A
ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX, HTRX1, MLL, MLL1, MLL1A, TRX1, WDSTS
Attention deficit hyperactivity disorder, Autism, Ptosis, Bipolar disorder, B-lymphoblastic leukemia/lymphoma, Hepatocellular carcinoma, Transitional cell carcinoma, Cornelia de lange syndrome, Desbuquois syndrome, Insomnia, Intellectual developmental disorder, Kabuki syndrome, Lethal congenital contracture syndrome, Myeloid leukemia, Major depressive disorder
View all (11 more)

215
Keratinocyte proline rich protein
C1orf45
Psoriasis

216
Potassium two pore domain channel subfamily K member 4
FHEIG, K2p4.1, TRAAK, TRAAK1
Facial dysmorphism syndrome, Intellectual developmental disorder

217
Kelch like family member 5
-
Asthma, Breast cancer, Acute lymphoblastic leukemia, Glaucoma

218
Lysine methyltransferase 5B
CGI-85, CGI85, MRD51, SUV420H1
Alzheimer disease, Autism, Breast cancer, Neurodevelopmental disorder, Global developmental delay, Gout, Intellectual developmental disorder, Intellectual developmental disorder dysmorphic hypotonia, Neural tube defect, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Schizophrenia

219
Potassium channel tetramerization domain containing 3
NY-REN-45
Attention deficit hyperactivity disorder, Autism, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay

220
Potassium two pore domain channel subfamily K member 9
BIBARS, K2p9.1, KT3.2, TASK-3, TASK3, TASK32
Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Birk-barel syndrome, Color vision deficiency, Colorectal cancer, Dementia, Developmental disability, Absence epilepsy, Major depressive disorder, Mood disorder, Obesity, Psychiatric disorders, Schizophrenia
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