EP300 Chromosome 22

EP300 lysine acetyltransferase
305 variants 305 Health Risk

Upload your DNA to see your personal genotypes for variants in EP300.

What This Gene Does
This gene encodes the adenovirus E1A-associated cellular p300 transcriptional co-activator protein. It functions as histone acetyltransferase that regulates transcription via chromatin remodeling and is important in the processes of cell proliferation and differentiation. It mediates cAMP-gene regulation by binding specifically to phosphorylated CREB protein. This gene has also been identified as a co-activator of HIF1A (hypoxia-inducible factor 1 alpha), and thus plays a role in the stimulation of hypoxia-induced genes such as VEGF. Defects in this gene are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
"Zinc fingers ZZ-type|Lysine acetyltransferases|Bromodomain containing"
Locus Type
gene with protein product
Location
22q13.2
Ensembl
ENSG00000100393
Associated Conditions (27)
Inborn genetic diseases
EP300-related disorder
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Rubinstein-Taybi syndrome
Rubinstein-Taybi syndrome due to CREBBP mutations
Colorectal cancer
Menke-Hennekam syndrome 2
Intellectual disability
See cases
Multicystic kidney dysplasia
Developmental and epileptic encephalopathy
18
Hepatoblastoma
Microcephaly
intellectual deficiency
Neurodevelopmental delay
Rare genetic intellectual disability
Multiple congenital anomalies
Carcinoma of colon
Uterine corpus endometrial carcinoma
+7 more conditions
Key Variants
RS1012101301
Conflicting classifications of pathogenicity
Inborn genetic diseases, EP300-related disorder, Inborn genetic diseases
Health Risk
RS115849119
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1169505007
Conflicting classifications of pathogenicity
Health Risk
RS1176732027
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1185038602
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, EP300-related disorder
Health Risk
RS1210404526
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1243111732
Conflicting classifications of pathogenicity
EP300-related disorder, Inborn genetic diseases, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1261612920
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to CREBBP mutations, Colorectal cancer, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1278019392
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1290732977
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Inborn genetic diseases, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1301322622
Conflicting classifications of pathogenicity
Inborn genetic diseases, EP300-related disorder, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
RS1308182502
Conflicting classifications of pathogenicity
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Health Risk
All Variants (305)
RSID Category Clinical Significance Conditions
RS875989807 Health Risk Conflicting classifications of pathogenicity Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, EP300-related disorder, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS886057571 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Inborn genetic diseases
RS887226313 Health Risk Conflicting classifications of pathogenicity Hepatoblastoma, EP300-related disorder, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS964396023 Health Risk Conflicting classifications of pathogenicity Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS980024399 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Inborn genetic diseases
RS1057518002 Health Risk Likely pathogenic
RS1057519012 Health Risk Likely pathogenic Microcephaly, intellectual deficiency, Microcephaly
RS1064795607 Health Risk Likely pathogenic
RS1085307564 Health Risk Likely pathogenic
RS1085307911 Health Risk Likely pathogenic
RS1340981566 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1379274045 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1464734494 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1555907286 Health Risk Likely pathogenic
RS1555910602 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1555911334 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1555912107 Health Risk Likely pathogenic
RS1555912238 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1555912362 Health Risk Likely pathogenic
RS1569120903 Health Risk Likely pathogenic Menke-Hennekam syndrome 2, Menke-Hennekam syndrome 2
RS1601617062 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1601629319 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to CREBBP mutations, Rubinstein-Taybi syndrome due to CREBBP mutations
RS1601633708 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1601636935 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to CREBBP mutations, Rubinstein-Taybi syndrome due to CREBBP mutations
RS1601639958 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS1601641819 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2058974109 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Colorectal cancer, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2059050708 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2059051273 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2059089321 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2059210417 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to CREBBP mutations, Rubinstein-Taybi syndrome due to CREBBP mutations
RS2059211409 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2059215587 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2059219404 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2059220495 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2059220693 Health Risk Likely pathogenic Menke-Hennekam syndrome 2, Menke-Hennekam syndrome 2
RS2145512909 Health Risk Likely pathogenic Menke-Hennekam syndrome 2, Menke-Hennekam syndrome 2
RS2145513922 Health Risk Likely pathogenic Neurodevelopmental delay, Neurodevelopmental delay
RS2145516075 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2145516079 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2145518271 Health Risk Likely pathogenic
RS2145519140 Health Risk Likely pathogenic
RS2145524882 Health Risk Likely pathogenic
RS2145734002 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2145740556 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2145744796 Health Risk Likely pathogenic
RS2145747771 Health Risk Likely pathogenic EP300-related disorder, EP300-related disorder
RS2145752629 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2145756375 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
RS2145766457 Health Risk Likely pathogenic Rubinstein-Taybi syndrome due to EP300 haploinsufficiency, Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
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