Show pageOld revisionsBacklinksFold/unfold allBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. ======= PTGFRN ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: PTGFRN * **<color #00a2e8>Official Name</color>**: prostaglandin F2 receptor inhibitor * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=5738|5738]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9P2B2|Q9P2B2]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=PTGFRN&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20PTGFRN|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/601204|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: N/A * **<color #00a2e8>UniProt Summary</color>**: Inhibits the binding of prostaglandin F2-alpha (PGF2- alpha) to its specific FP receptor, by decreasing the receptor number rather than the affinity constant. Functional coupling with the prostaglandin F2-alpha receptor seems to occur (By similarity). {ECO:0000250}. <button type='primary' 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'> |V-set| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |myoblast fusion involved in skeletal muscle regeneration| |myotube differentiation involved in skeletal muscle regeneration| |lipid droplet organization| |myoblast fusion| |skeletal muscle tissue regeneration| |syncytium formation by plasma membrane fusion| |cell-cell fusion| |syncytium formation| |myotube differentiation| |tissue regeneration| |regeneration| |striated muscle cell differentiation| |muscle cell differentiation| |developmental growth| |growth| |muscle structure development| |wound healing| |response to wounding| |cell surface| |anatomical structure formation involved in morphogenesis| |endoplasmic reticulum membrane| |Golgi apparatus| |tissue development| </modal> \\ === CRISPR Data === <button type='primary' 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'> ^Screen^Score^ |[[:results:exp477|DKK1 89ng/ml R08 exp477]]|-1.78| |[[:results:exp320|ABT-702 5μM plus CoCl2 18μM R07 exp320]]|-1.73| |[[:results:exp351|Dexamethasone 0.006μM R07 exp351]]|-1.71| </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: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 5818 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 2.67 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='PTGFRN Expression in NALM6 Cells: 2.67'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1