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Ask your administrator if you think this is wrong. ======= PAGR1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: PAGR1 * **<color #00a2e8>Official Name</color>**: PAXIP1 associated glutamate rich protein 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=79447|79447]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9BTK6|Q9BTK6]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=PAGR1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20PAGR1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/612033|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: N/A * **<color #00a2e8>UniProt Summary</color>**: Its association with the histone methyltransferase MLL2/MLL3 complex is suggesting a role in epigenetic transcriptional activation. However, in association with PAXIP1/PTIP is proposed to function at least in part independently of the MLL2/MLL3 complex. Proposed to be recruited by PAXIP1 to sites of DNA damage where the PAGR1:PAXIP1 complex is required for cell survival in response to DNA damage independently of the MLL2/MLL3 complex (PubMed:19124460). However, its function in DNA damage has been questioned (By similarity). During immunoglobulin class switching in activated B-cells is involved in transcription regulation of downstream switch regions at the immunoglobulin heavy-chain (Igh) locus independently of the MLL2/MLL3 complex (By similarity). Involved in both estrogen receptor-regulated gene transcription and estrogen-stimulated G1/S cell-cycle transition (PubMed:19039327). Acts as transcriptional cofactor for nuclear hormone receptors. Inhibits the induction properties of several steroid receptors such as NR3C1, AR and PPARG; the mechanism of inhibition appears to be gene-dependent (PubMed:23161582). {ECO:0000250|UniProtKB:Q99L02, ECO:0000269|PubMed:19039327, ECO:0000269|PubMed:19124460, ECO:0000269|PubMed:23161582, ECO:0000305}. <button type='default' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> No Pfam Domain information is available for this gene. </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |positive regulation of intracellular estrogen receptor signaling pathway| |MLL3/4 complex| |positive regulation of intracellular steroid hormone receptor signaling pathway| |histone H3-K4 methylation| |regulation of intracellular estrogen receptor signaling pathway| |histone methyltransferase complex| |estrogen receptor binding| |positive regulation of cell cycle G1/S phase transition| |histone lysine methylation| |regulation of intracellular steroid hormone receptor signaling pathway| |peptidyl-lysine methylation| |histone methylation| |positive regulation of cell cycle phase transition| |protein methylation| |protein alkylation| |regulation of cell cycle G1/S phase transition| |DNA recombination| |macromolecule methylation| |positive regulation of cell cycle process| |methylation| |peptidyl-lysine modification| |histone modification| |covalent chromatin modification| |positive regulation of cell cycle| |regulation of cell cycle phase transition| |DNA repair| |chromatin organization| |DNA metabolic process| |regulation of cell cycle process| |cellular response to DNA damage stimulus| |peptidyl-amino acid modification| |chromosome organization| |regulation of cell cycle| |positive regulation of transcription by RNA polymerase II| |positive regulation of transcription, DNA-templated| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |positive regulation of signal transduction| |cellular response to stress| |positive regulation of RNA metabolic process| |positive regulation of cell communication| |positive regulation of signaling| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| </modal> \\ === CRISPR Data === <button type='default' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> No hits were found. </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 25/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|2/28| |bone|0/25| |breast|2/33| |central nervous system|1/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|1/15| |kidney|1/21| |liver|2/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|2/24| |soft tissue|1/7| |thyroid|0/2| |upper aerodigestive|3/22| |urinary tract|2/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 2618 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 6.26 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='PAGR1 Expression in NALM6 Cells: 6.26'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:36by 127.0.0.1