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YOR244W ESA1 / SGDID:S000005770

SGD CSV

Yeast Systematic Name	Yeast Symbol	SGDID	Analog Name	Analog Description	EC	Organism	Disease	Structure	Uniprot	Human ID	Human Symbol	HHsearch Probability	HHsearch E_value	HHsearch P_value	HHsearch Score	Flag Disease related	Flag Homo sapiens
YOR244W	ESA1	SGDID:S000005770	KAT5 HTATIP TIP60	Histone acetyltransferase KAT5 (EC 2.3.1.48) (60 kDa Tat-interactive protein) (Tip60) (Histone acetyltransferase HTATIP) (HIV-1 Tat interactive protein) (Lysine acetyltransferase 5) (cPLA(2)-interacting protein)	2.3.1.48	Homo sapiens	Neurodevelopmental Disorder With Dysmorphic Facies, Sleep Disturbance, And Brain Abnormalities,Primary Hyperoxaluria,Colorectal Cancer,Human Immunodeficiency Virus Type 1,Prostate Cancer,Aicardi-Goutieres Syndrome 3,Chromosome 16p13.3 Deletion Syndrome, Proximal,Aicardi-Goutieres Syndrome,Immune Deficiency Disease	2ou2_a	Q92993	ENSG00000172977	KAT5	100.00	4.40E-65	3.50E-69	499.10	1	1
YOR244W	ESA1	SGDID:S000005770	ESA1 YOR244W O5257	Histone acetyltransferase ESA1 (EC 2.3.1.48)	2.3.1.48	Saccharomyces cerevisiae		3to7_a	Q08649			100.00	6.90E-67	5.40E-71	510.20	0	0
YOR244W	ESA1	SGDID:S000005770	ESA1 YOR244W O5257	Histone acetyltransferase ESA1 (EC 2.3.1.48)	2.3.1.48	Saccharomyces cerevisiae		1fy7_a	Q08649			100.00	2.60E-76	1.90E-80	565.30	0	0
YOR244W	ESA1	SGDID:S000005770	KAT8 MOF MYST1 PP7073	Histone acetyltransferase KAT8 (EC 2.3.1.48) (Lysine acetyltransferase 8) (MOZ, YBF2/SAS3, SAS2 and TIP60 protein 1) (MYST-1) (hMOF)	2.3.1.48	Homo sapiens	Capgras Syndrome,Koolen-De Vries Syndrome,Syndromic Intellectual Disability,Li-Ghorbani-Weisz-Hubshman Syndrome,Medulloblastoma	2pq8_a	Q9H7Z6	ENSG00000103510	KAT8	100.00	6.10E-65	4.80E-69	497.20	1	1
YOR244W	ESA1	SGDID:S000005770	KAT6A MOZ MYST3 RUNXBP2 ZNF220	Histone acetyltransferase KAT6A (EC 2.3.1.48) (MOZ, YBF2/SAS3, SAS2 and TIP60 protein 3) (MYST-3) (Monocytic leukemia zinc finger protein) (Runt-related transcription factor-binding protein 2) (Zinc finger protein 220)	2.3.1.48	Homo sapiens	Chronic Myelomonocytic Leukemia,Leukemia,Neonatal Leukemia,Leukemia, Acute Myeloid,Acute Myeloid Leukemia With T(8;16)(P11;P13) Translocation,Monocytic Leukemia,Microcephaly,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Ohdo Syndrome, Sbbys Variant,Chromosome 16p13.3 Deletion Syndrome, Proximal,Myelodysplastic Syndrome,Arboleda-Tham Syndrome,Acute Promyelocytic Leukemia,Syndromic Intellectual Disability,Autism Spectrum Disorder,Ohdo Syndrome,Leukemia, Acute Monocytic,Autosomal Dominant Non-Syndromic Intellectual Disability,Autism	2ozu_a	Q92794	ENSG00000083168	KAT6A	100.00	9.80E-64	7.80E-68	490.20	1	1
YOR244W	ESA1	SGDID:S000005770	KAT7 HBO1 HBOa MYST2	Histone acetyltransferase KAT7 (EC 2.3.1.48) (Histone acetyltransferase binding to ORC1) (Lysine acetyltransferase 7) (MOZ, YBF2/SAS3, SAS2 and TIP60 protein 2) (MYST-2)	2.3.1.48	Homo sapiens	Hemangioma Of Spleen,Ovarian Endodermal Sinus Tumor,Ovarian Primitive Germ Cell Tumor,Kleefstra Syndrome 1	5gk9_a	O95251	ENSG00000136504	KAT7	100.00	1.90E-63	1.50E-67	486.50	1	1