Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "K"

11 to 20 of 429 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	57325	KAT14	Lysine acetyltransferase 14	ATAC2, CRP2BP, CSRP2BP, PRO1194, dJ717M23.1	Global developmental delay, Mitochondrial complex deficiency
12	2648	KAT2A	Lysine acetyltransferase 2A	GCN5, GCN5L2, PCAF-b, hGCN5	Coronary artery disease, Crohn disease, Inflammatory bowel disease, Ulcerative colitis
13	8850	KAT2B	Lysine acetyltransferase 2B	CAF, P/CAF, PCAF	Androgenetic alopecia, Bipolar disorder, Insomnia, Kidney cancer, Major depressive disorder, Mood disorder, Post-traumatic stress disorder, Schizophrenia, Stroke
14	10524	KAT5	Lysine acetyltransferase 5	ESA1, HTATIP, HTATIP1, NEDFASB, PLIP, TIP, TIP60, ZC2HC5, cPLA2	Eczema, Diabetes mellitus, Hypertension, Gout, Mesothelioma, Metabolic syndrome, Neurodevelopmental disorder, Diabetes mellitus type 2
15	7994	KAT6A	Lysine acetyltransferase 6A	ARTHS, MOZ, MRD32, MYST-3, MYST3, RUNXBP2, ZC2HC6A, ZNF220	Arboleda-tham syndrome, Autism, Intellectual disability with craniofacial anomalies and cardiac defects, Adenoid cystic carcinoma, Craniosynostosis, Developmental delay, Global developmental delay, Intellectual developmental disorder, Medulloblastoma, Neurodevelopmental disorder, Prostatic neoplasms, Diabetes mellitus type 2, Vein of galen aneurysm
16	23522	KAT6B	Lysine acetyltransferase 6B	GTPTS, MORF, MOZ2, MYST4, ZC2HC6B, qkf, querkopf	Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps, Arachnodactyly, Juvenile arthritis, Bipolar disorder, Blepharophimosis syndrome, Blepharophimosis-intellectual disability syndrome, Congenital anomalies of the kidney and urinary tract, Congenital clubfoot, Congenital epicanthus, Congenital hypoplasia of kidney, Craniosynostosis, Cryptorchidism, Bipolar depression, Desbuquois syndrome, Developmental delay View all (15 more)
17	84148	KAT8	Lysine acetyltransferase 8	LIGOWS, MOF, MYST1, ZC2HC8, hMOF	Alzheimer disease, Cardiomyopathy, Congestive heart failure, Heart failure, Hypertrophic cardiomyopathy, Metabolic syndrome, Non-specific syndromic intellectual disability, Psoriasis, Schizophrenia, Diabetes mellitus type 2
18	11104	KATNA1	Katanin catalytic subunit A1	-	Central nervous system cancer, Glioblastoma, Glioma, Lung cancer, Squamous cell carcinoma, Testicular carcinoma, Testicular germ cell tumor
19	84056	KATNAL1	Katanin catalytic subunit A1 like 1	-	Androgenetic alopecia, Anti-neutrophil antibody associated vasculitis, Diabetes mellitus type 2
20	83473	KATNAL2	Katanin catalytic subunit A1 like 2	-	Alzheimer disease, Color vision deficiency, Neurodevelopmental disorder, Dementia, Non-specific syndromic intellectual disability, Schizophrenia

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