Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

81 to 90 of 320 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
81	23704	KCNE4	Potassium voltage-gated channel subfamily E regulatory subunit 4	MIRP3	Cardiac embolism, Cardioembolic stroke, Acute lymphoblastic leukemia, Hepatitis b, Oropharyngeal cancer
82	24137	KIF4A	Kinesin family member 4A	KIF4, KIF4G1, MRX100, TMDI, XLID100	Hepatocellular carcinoma, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Neurodevelopmental disorder, Hydrocephalus, Intellectual developmental disorder, x-linked, Obesity
83	2531	KDSR	3-ketodihydrosphingosine reductase	DHSR, EKVP4, FVT1, SDR35C1	Erythrokeratodermia variabilis, Lymphoma, Melanoma, Prostate cancer, Schizophrenia
84	25818	KLK5	Kallikrein related peptidase 5	KLK-L2, KLKL2, SCTE	Prostatic neoplasm
85	25959	KANK2	KN motif and ankyrin repeat domains 2	ANKRD25, MXRA3, NPHS16, PPKWH, SIP	Bronchial disease, Cardiovascular disease, Carpal tunnel syndrome, Coronary artery disease, Genetic steroid-resistant nephrotic syndrome, Heart failure, Steroid-resistant nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, Open angle glaucoma, Diabetes mellitus, type 2, Woolly hair-palmoplantar keratoderma syndrome
86	26128	KIFBP	Kinesin family binding protein	KBP, KIAA1279, KIF1BP, TTC20	Color vision deficiency, Coronary artery disease, Intellectual developmental disorder, Cortical development malformation, Microcephaly, Peripheral neuropathy, Schizophrenia
87	26249	KLHL3	Kelch like family member 3	PHA2D	Alzheimer disease, Atrial fibrillation, Cerebral palsy, Color vision deficiency, Dementia, Heart failure, Pseudohypoparathyroidism, Schizophrenia
88	2648	KAT2A	Lysine acetyltransferase 2A	GCN5, GCN5L2, PCAF-b, hGCN5	Coronary artery disease, Crohn disease, Inflammatory bowel disease, Ulcerative colitis
89	27133	KCNH5	Potassium voltage-gated channel subfamily H member 5	DEE112, EAG2, H-EAG2, Kv10.2, hEAG2	Alzheimer disease, Aneurysm, Aortic aneurysm, Color vision deficiency, Conotruncal cardiac defect, Developmental and epileptic encephalopathy, Gastroesophageal reflux disease, Major depressive disorder, Metabolic syndrome, Diabetes mellitus, type 2
90	283455	KSR2	Kinase suppressor of ras 2	-	Androgenetic alopecia, Autism, Central nervous system cancer, Cerebral amyloid angiopathy, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Endometriosis, Glioblastoma, Glioma, Hyperlipidemia, Hypertension, Insomnia, Alzheimer disease, Major depressive disorder View all (7 more)

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