Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6571 to 6580 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6571
Lysine acetyltransferase 14
ATAC2, CRP2BP, CSRP2BP, PRO1194, dJ717M23.1
Global developmental delay, Mitochondrial complex deficiency

6572
Lysine acetyltransferase 2A
GCN5, GCN5L2, PCAF-b, hGCN5
Coronary artery disease, Crohn disease, Inflammatory bowel disease, Ulcerative colitis

6573
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

6574
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

6575
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

6576
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
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6577
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

6578
Katanin catalytic subunit A1
-
Central nervous system cancer, Glioblastoma, Glioma, Lung cancer, Squamous cell carcinoma, Testicular carcinoma, Testicular germ cell tumor

6579
Katanin catalytic subunit A1 like 1
-
Androgenetic alopecia, Anti-neutrophil antibody associated vasculitis, Diabetes mellitus type 2

6580
Katanin catalytic subunit A1 like 2
-
Alzheimer disease, Color vision deficiency, Neurodevelopmental disorder, Dementia, Non-specific syndromic intellectual disability, Schizophrenia