Protein Information

Cytoscape View


UniProt AC / UniProt ID P13056 / NR2C1_HUMAN
Protein Name Nuclear receptor subfamily 2 group C member 1
Gene Name Name: NR2C1
Synonyms:TR2;
Organism Homo sapiens (Human)

PRO ID PR:P13056
DAG View
PRO Name nuclear receptor subfamily 2 group C member 1 (human)
Definition A nuclear receptor subfamily 2 group C member 1 that is encoded in the genome of human.
Short Label hNR2C1
Category organism-gene

Interactive Sequence View

Select/align proteoforms across species


P13056 (NR2C1) as Substrate



Site PTM Type PTM Enzyme Score Source PMID
K42 Ubiquitination PhosphoSitePlus
T53 Phosphorylation PhosphoSitePlus
K56 Ubiquitination PhosphoSitePlus
S64 Phosphorylation IEDB   PhosphoSitePlus 32387766
T98 Phosphorylation PhosphoSitePlus
K119 Ubiquitination PhosphoSitePlus
S148 O-Glycosylation GlyGen 30379171
K188 Ubiquitination PhosphoSitePlus
K196 Acetylation PhosphoSitePlus
S215 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 18669648, 23186163
T218 Phosphorylation phospho.ELM   PhosphoSitePlus 18669648
T220 Phosphorylation phospho.ELM   PhosphoSitePlus   UniProt 18669648
Y392 Phosphorylation PhosphoSitePlus
K523 Ubiquitination PhosphoSitePlus
K538 Ubiquitination PhosphoSitePlus
S581 O-Glycosylation GlyGen 30379171
Site PTM Type PTM Enzyme Score Source PMID
S215 Phosphorylation HPRD 18669648, 18452278
T218 Phosphorylation HPRD 18669648, 20068231
T220 Phosphorylation HPRD 18669648
Site PTM Type PTM Enzyme Score Source PMID
S215 Phosphorylation HPRD 18669648, 18452278
T218 Phosphorylation HPRD 18669648, 20068231
T220 Phosphorylation HPRD 18669648


PTM sites affected in variants

Site Variant Source PMID Disease [Sample source]
S148 L148 Biomuta DOID:4159 / skin cancer [ cosmic ]