|Institutional Source||Beutler Lab|
|Gene Name||E1A binding protein p300|
|Is this an essential gene?||Essential (E-score: 1.000)|
|Stock #||R6599 (G1)|
|Chromosomal Location||81585351-81652077 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||G to C at 81586713 bp (GRCm38)|
|Amino Acid Change||Aspartic acid to Histidine at position 29 (D29H)|
|Ref Sequence||ENSEMBL: ENSMUSP00000066789 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000068387]|
AA Change: D29H
AA Change: D29H
|Meta Mutation Damage Score||0.3325|
|Coding Region Coverage||
|Validation Efficiency||94% (32/34)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 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]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit defects of the heart, lung, and small intestine and die at midgestation; heterozygotes also show some embryonic loss. Heterozygotes for an acetyltransferase-negative mutation die by the neonatal period. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Ep300||
(F):5'- ACCATTTCTGTTGAGTCCGC -3'
(R):5'- AAATGGTTGGGCTACTGGACG -3'
(F):5'- AGCCCACCCTTAGGAGC -3'
(R):5'- GCTACTGGACGTCTTCGAC -3'