NR3C1 |
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![](//upload.wikimedia.org/wikipedia/commons/thumb/f/f0/Glucocorticoid_receptor.png/250px-Glucocorticoid_receptor.png) |
Strwythurau |
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PDB | Human UniProt search: PDBe RCSB |
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Rhestr o ddynodwyr PDB |
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1M2Z, 1NHZ, 1P93, 3BQD, 3CLD, 3E7C, 3H52, 3K22, 3K23, 4CSJ, 4HN5, 4HN6, 4LSJ, 4MDD, 4P6W, 4P6X, 5CBY, 5CBX, 4UDC, 4UDD, 5CBZ, 5CC1, 5EMQ, 5EMC, 5EMP |
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Dynodwyr |
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Cyfenwau | NR3C1, GCCR, GCR, GCRST, GR, GRL, nuclear receptor subfamily 3 group C member 1, Glucocorticoid Receptor |
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Dynodwyr allanol | OMIM: 138040 HomoloGene: 30960 GeneCards: NR3C1 |
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Ontoleg y genyn |
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Gweithrediad moleciwlaidd | • steroid hormone binding • DNA binding • sequence-specific DNA binding • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity • zinc ion binding • GO:0001077, GO:0001212, GO:0001213, GO:0001211, GO:0001205 DNA-binding transcription activator activity, RNA polymerase II-specific • glucocorticoid receptor activity • GO:0038050, GO:0004886, GO:0038051 nuclear receptor activity • metal ion binding • GO:0000980 RNA polymerase II cis-regulatory region sequence-specific DNA binding • steroid hormone receptor activity • steroid binding • GO:0001948, GO:0016582 protein binding • lipid binding • RNA binding • SUMO binding • Hsp90 protein binding • GO:0001200, GO:0001133, GO:0001201 DNA-binding transcription factor activity, RNA polymerase II-specific • protein kinase binding
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Cydrannau o'r gell | • cytoplasm • nucleoplasm • mitochondrial matrix • mitocondria • cnewyllyn cell • Cytosgerbwd • spindle • microtubule organizing center • cytosol • nuclear speck • GO:0009327 protein-containing complex
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Prosesau biolegol | • cellular response to steroid hormone stimulus • GO:0009373 regulation of transcription, DNA-templated • glucocorticoid mediated signaling pathway • transcription by RNA polymerase II • transcription initiation from RNA polymerase II promoter • glucocorticoid receptor signaling pathway • GO:0072468 signal transduction • steroid hormone mediated signaling pathway • cell cycle • Cellraniad • GO:0097285 apoptotic process • chromosome segregation • GO:1901227 negative regulation of transcription by RNA polymerase II • transcription, DNA-templated • cellular response to dexamethasone stimulus • cellular response to transforming growth factor beta stimulus • GO:0003257, GO:0010735, GO:1901228, GO:1900622, GO:1904488 positive regulation of transcription by RNA polymerase II • cellular response to glucocorticoid stimulus • GO:0031497, GO:0006336, GO:0034724, GO:0001301, GO:0007580, GO:0034652, GO:0010847 chromatin organization • positive regulation of pri-miRNA transcription by RNA polymerase II
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Sources:Amigo / QuickGO |
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Orthologau |
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Species | Bod dynol | Llygoden |
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Entrez | | |
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Ensembl | | |
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UniProt | | |
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RefSeq (mRNA) | | |
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RefSeq (protein) | | |
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Lleoliad (UCSC) | n/a | n/a |
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PubMed search | [1] | n/a |
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Wicidata |
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Protein sy'n cael ei godio yn y corff dynol gan y genyn NR3C1 yw NR3C1 a elwir hefyd yn Glucocorticoid receptor (Saesneg). Segment o DNA yw'r genyn, sy'n amgodio ffwythiant arbennig. Mae'r genyn yma wedi ei leoli ar yr edefyn ôl o gromosom dynol 5, band 5q31.3.[2]
Yn aml mae gan enynnau lawer o gyfystyron. Mae hyn oherwydd eu bod yn aml yn cael eu darganfod gan nifer o bobl mewn cyd-destunau gwahanol heb wybod mai'r un genynnau oeddyn nhw. Hefyd mae gan wahanol gymunedau gwyddonol safonau gwahanol ar gyfer enwi genynnau. Dyma restr o gyfystyron ar gyfer y genyn NR3C1.
- "Generating diversity in human glucocorticoid signaling through a racially diverse polymorphism in the beta isoform of the glucocorticoid receptor. ". Lab Invest. 2017. PMID 28759007.
- "Glucocorticoid receptor polymorphism in obesity and glucose homeostasis. ". Adv Clin Exp Med. 2017. PMID 28397446.
- "Glucocorticoid receptor variants in childhood attention-deficit/hyperactivity disorder and comorbid psychiatric disorders. ". Psychiatry Res. 2016. PMID 27741480.
- "Glomerular Glucocorticoid Receptors Expression and Clinicopathological Types of Childhood Nephrotic Syndrome. ". Fetal Pediatr Pathol. 2017. PMID 27690709.
- "Medical morbidities and DNA methylation of NR3C1 in preterm infants.". Pediatr Res. 2017. PMID 27653086.