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Details on Person UniProt:Q15466 NR0B2

Class:IdReferenceGeneProduct:64444
_chainChangeLogchain:1-257 added on Fri February 6 2015
_displayNameUniProt:Q15466 NR0B2
_timestamp2026-02-20 22:57:46
chainchain:1-257
checksum14BEE2B3FF46154A
commentFUNCTION Transcriptional regulator that acts as a negative regulator of receptor-dependent signaling pathways (PubMed:22504882). Specifically inhibits transactivation of the nuclear receptor with which it interacts (PubMed:22504882). Inhibits transcriptional activity of NEUROD1 on E-box-containing promoter by interfering with the coactivation function of the p300/CBP-mediated transcription complex for NEUROD1 (PubMed:14752053). Essential component of the liver circadian clock which via its interaction with NR1D1 and RORG regulates NPAS2-mediated hepatic lipid metabolism (By similarity). Regulates the circadian expression of cytochrome P450 (CYP) enzymes (By similarity). Represses: NR5A2 and HNF4A to down-regulate CYP2C38, NFLI3 to up-regulate CYP2A5, BHLHE41/HNF1A axis to up-regulate CYP1A2, CYP2E1 and CYP3A11, and NR1D1 to up-regulate CYP2B10, CYP4A10 and CYP4A14 (By similarity).SUBUNIT Interacts (via N-terminus) with NEUROD1 (via N-terminus and C-terminus) (PubMed:14752053). Interacts with ID2 (PubMed:14752053). Interacts with RORG, NFIL3, NR1D1 and BHLHE41 (By similarity). Heterodimer; efficient DNA binding requires dimerization with another bHLH protein (PubMed:14752053). Interacts with RARA, RXRA, THRB, NR5A1, NR5A2, NR1I3, PPARA, PPARG and EID1 (PubMed:22504882). Interacts with HNF4A; the resulting heterodimer is transcriptionally inactive (PubMed:28128295). Interacts with DDX3X; this interaction disrupts the interaction between HNF4 and NR0B2/SHP that forms inactive heterodimers and enhances the formation of active HNF4 homodimers (PubMed:28128295).INTERACTION Colocalizes with NEUROD1 in the nucleus.TISSUE SPECIFICITY Liver. Low levels of expression were detected in heart and pancreas.PTM Arginine methylation by PRMT5 enhances repression activity of metabolic genes in liver in response to bile acid signaling, by increasing interaction with cofactors.DISEASE Disease susceptibility is associated with variants affecting the gene represented in this entry.SIMILARITY Belongs to the nuclear hormone receptor family. NR0 subfamily.
descriptionrecommendedName: Nuclear receptor subfamily 0 group B member 2 alternativeName: Orphan nuclear receptor SHP alternativeName: Small heterodimer partner
geneNameNR0B2
SHP
identifierQ15466
isSequenceChangedFALSE
keyword3D-structure
Biological rhythms
Cytoplasm
Disease variant
Methylation
Nucleus
Obesity
Proteomics identification
Receptor
Reference proteome
Repressor
Transcription
Transcription regulation
modified[InstanceEdit:9836292] Weiser, Joel, 2023-05-25
[InstanceEdit:9852000] Weiser, Joel, 2023-11-03
[InstanceEdit:9862192] Weiser, Joel, 2024-02-26
[InstanceEdit:9939033] Weiser, Joel, 2025-02-21
[InstanceEdit:9983091] Weiser, Joel, 2026-02-20
nameNR0B2
referenceDatabase[ReferenceDatabase:2] UniProt
referenceGene[ReferenceDNASequence:8990859] ENSEMBL:ENSG00000131910 NR0B2 [Homo sapiens]
secondaryIdentifierNR0B2_HUMAN
F1D8P5
Q5QP36
sequenceLength257
species[Species:48887] Homo sapiens
(referenceEntity)[EntityWithAccessionedSequence:376312] NR0B2 [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9712456] NR0B2 [cytosol] [Homo sapiens]
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No pathways have been reviewed or authored by UniProt:Q15466 NR0B2 (64444)