Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

241 to 250 of 320 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
241	5655	KLK10	Kallikrein related peptidase 10	NES1, PRSSL1	Breast neoplasm, Ovarian neoplasm, Stomach neoplasms
242	56992	KIF15	Kinesin family member 15	BRDCS2, HKLP2, KLP2, KNSL7, NY-BR-62	21q22.11q22.12 microdeletion syndrome, Bipolar disorder, Hepatocellular carcinoma, Idiopathic pulmonary fibrosis, Iga nephropathy, Major depressive disorder, Metabolic syndrome, Diabetes mellitus, type 2
243	57082	KNL1	Kinetochore scaffold 1	AF15Q14, CASC5, CT29, D40, MCPH4, PPP1R55, Spc7, hKNL-1, hSpc105	Primary microcephaly, Congenital muscular dystrophy, Idiopathic pulmonary fibrosis, Microcephaly, Prostate cancer, Diabetes mellitus, type 2
244	57325	KAT14	Lysine acetyltransferase 14	ATAC2, CRP2BP, CSRP2BP, PRO1194, dJ717M23.1	Global developmental delay, Mitochondrial complex deficiency
245	57498	KIDINS220	Kinase D interacting substrate 220	ARMS, SINO, VENARG	Cerebral palsy, Color vision deficiency, Kabuki syndrome
246	57576	KIF17	Kinesin family member 17	KIF17B, KIF3X, KLP-2, OSM-3	Autism, Color vision deficiency, Eosinophilia, Schizophrenia, Diabetes mellitus, type 1
247	57582	KCNT1	Potassium sodium-activated channel subfamily T member 1	DEE14, EIEE14, ENFL5, KCa4.1, KNa1.1, SLACK, Slo2.2, bA100C15.2	Nocturnal frontal lobe epilepsy, Childhood-onset epilepsy syndrome, Color vision deficiency, Colorectal cancer, Developmental and epileptic encephalopathy, Developmental disability, Partial epilepsy, Epilepsy of infancy with migrating focal seizures, Frontal lobe epilepsy, Rolandic epilepsy, Gastrointestinal disease, Hydrocephalus, Malignant migrating partial seizures of infancy, Neurodevelopmental disorders, Schizophrenia, Scoliosis View all (1 more)
248	57670	KIAA1549	KIAA1549	RP86	Astrocytoma, Oligodendroglioma, Optic atrophy, Retinitis pigmentosa, Schizophrenia
249	58508	KMT2C	Lysine methyltransferase 2C	HALR, KLEFS2, MLL3	Alzheimer disease, Autism, Adenoid cystic carcinoma, Hepatocellular carcinoma, Transitional cell carcinoma, Cerebellar atrophy, Cholangiocarcinoma, Developmental and epileptic encephalopathy, Esophageal squamous cell carcinoma, Global developmental delay, Hypertrophic cardiomyopathy, Intellectual developmental disorder, Kleefstra syndrome, Myeloid leukemia, Liver disease View all (5 more)
250	5927	KDM5A	Lysine demethylase 5A	NEDEHC, RBBP-2, RBBP2, RBP2	Ankylosing spondylitis, Congenital heart disease, Intellectual developmental disorder, Neurodevelopmental disorders, Diabetes mellitus, type 2

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