Entity Details

Primary name NRIP1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP48552
EntryNameNRIP1_HUMAN
FullNameNuclear receptor-interacting protein 1
TaxID9606
Evidenceevidence at protein level
Length1158
SequenceStatuscomplete
DateCreated1996-02-01
DateModified2021-06-02

Ontological Relatives

GenesNRIP1

GO terms

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GOName
GO:0000118 histone deacetylase complex
GO:0000122 negative regulation of transcription by RNA polymerase II
GO:0000785 chromatin
GO:0000978 RNA polymerase II cis-regulatory region sequence-specific DNA binding
GO:0001543 ovarian follicle rupture
GO:0001650 fibrillar center
GO:0003713 transcription coactivator activity
GO:0003714 transcription corepressor activity
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005730 nucleolus
GO:0005829 cytosol
GO:0007623 circadian rhythm
GO:0016607 nuclear speck
GO:0019915 lipid storage
GO:0030331 estrogen receptor binding
GO:0030522 intracellular receptor signaling pathway
GO:0032922 circadian regulation of gene expression
GO:0035259 glucocorticoid receptor binding
GO:0042826 histone deacetylase binding
GO:0045944 positive regulation of transcription by RNA polymerase II
GO:0046965 retinoid X receptor binding
GO:0071392 cellular response to estradiol stimulus

Subcellular Location

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Subcellular Location
Nucleus

Domains

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DomainNameCategoryType
IPR026649 Nuclear receptor-interacting protein 1FamilyFamily
IPR031405 Nuclear receptor-interacting protein 1, repression domain 1DomainDomain
IPR031406 Nuclear receptor-interacting protein 1, repression domain 2DomainDomain
IPR031407 Nuclear receptor-interacting protein 1, repression domain 3FamilyFamily
IPR031408 Nuclear receptor-interacting protein 1, repression domain 4DomainDomain

Diseases

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Disease IDSourceNameDescription
618270 OMIMCongenital anomalies of kidney and urinary tract 3 (CAKUT3)A disorder encompassing a broad spectrum of renal and urinary tract malformations that include renal agenesis, kidney hypodysplasia, multicystic kidney dysplasia, duplex collecting system, posterior urethral valves and ureter abnormalities. Congenital anomalies of kidney and urinary tract are the commonest cause of chronic kidney disease in children. CAKUT3 inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB06884 4-HYDROXY-N'-(4-ISOPROPYLBENZYL)BENZOHYDRAZIDEDrugbanksmall molecule

Interactions

65 interactions

InteractorPartnerSourcesPublicationsLink
NRIP1_HUMAN1433F_HUMANHPRD, MINT11266503 details
NRIP1_HUMANLDOC1_HUMANBioGRID, HPRD, IntAct16189514 19060904 details
NRIP1_HUMANTEX11_HUMANBioGRID, HPRD, IntAct16189514 details
NRIP1_HUMANCEP70_HUMANBioGRID, HPRD, IntAct16189514 19060904 details
NRIP1_HUMANCTBP2_HUMANBioGRID, HPRD, IntAct15060175 16189514 details
NRIP1_HUMANTRAF2_HUMANBioGRID, HPRD, IntAct16189514 details
NRIP1_HUMANCC85B_HUMANBioGRID, HPRD, IntAct16189514 details
NRIP1_HUMANANM1_HUMANBioGRID, HPRD, MINT17053781 details
NRIP1_HUMANHDAC3_HUMANBioGRID, HPRD, MINT11006275 17053781 21868449 details
NRIP1_HUMANRARA_HUMANBioGRID, HPRD, IntAct, MINT10082574 10531331 12503607 12549917 14581481 16713569 17641689 25416956 8887632 details
NRIP1_HUMANDNMT1_HUMANBioGRID, MINT17972916 details
NRIP1_HUMANDNM3A_HUMANBioGRID, MINT17972916 details
NRIP1_HUMANDNM3B_HUMANBioGRID, MINT17972916 details
NRIP1_HUMANFHL1_HUMANBioGRID, IntAct19401155 details
NRIP1_HUMANESR1_HUMANBioGRID, HPRD, IntAct16439465 21182203 23403292 26153859 26166704 7641693 8887632 9115274 9192902 details
NRIP1_HUMANESR2_HUMANBioGRID, HPRD, IntAct11500849 15604093 21182203 details
NRIP1_HUMANTULP3_HUMANBioGRID, IntAct23414517 details
NRIP1_HUMANCTBP1_HUMANBioGRID, HPRD, IntAct, UniProt11509661 15060175 17085477 17972916 18374649 24722188 details
NRIP1_HUMANZN366_HUMANUniProt17085477 details
NRIP1_HUMANARPC3_HUMANBioGRID, IntAct25416956 details
NRIP1_HUMANGOGA2_HUMANIntAct32296183 details
NRIP1_HUMANPKNX2_HUMANBioGRID, IntAct32296183 details
NRIP1_HUMANERR3_HUMANBioGRID, HPRD, IntAct15604093 16439465 31515488 32296183 details
NRIP1_HUMANBHLH9_HUMANBioGRID, IntAct32296183 details
NRIP1_HUMANTHA_HUMANBioGRID, IntAct10379889 15130509 20211142 21868449 9626662 details
NRIP1_HUMANGCR_HUMANBioGRID, HPRD, IntAct10364267 10659697 11266503 12773562 20211142 31182584 details
NRIP1_HUMANSTF1_HUMANBioGRID, HPRD11459805 12782406 details
NRIP1_HUMANNR0B1_HUMANBioGRID, HPRD11459805 details
NRIP1_HUMANHDAC5_HUMANBioGRID, HPRD15060175 details
NRIP1_HUMAN1433T_HUMANBioGRID11266503 details
NRIP1_HUMANRXRA_HUMANBioGRID, HPRD12549917 8887632 details
NRIP1_HUMANAHR_HUMANBioGRID, HPRD10428779 11551916 details
NRIP1_HUMANPPARA_HUMANBioGRID9626662 details
NRIP1_HUMANPPARG_HUMANBioGRID, HPRD11500849 11877444 19596656 9626662 details
NRIP1_HUMANRXRB_HUMANBioGRID, HPRD11278635 12403842 12549917 9013766 9626662 details
NRIP1_HUMANJUN_HUMANBioGRID, HPRD12554755 details
NRIP1_HUMANERR1_HUMANBioGRID15604093 16439465 details
NRIP1_HUMANERR2_HUMANBioGRID16439465 details
NRIP1_HUMANE2F1_HUMANBioGRID20410059 22629304 details
NRIP1_HUMANACTN2_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANCIB1_HUMANBioGRID15604093 details
NRIP1_HUMANNR1H2_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANTHB_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANNR1H3_HUMANBioGRID, HPRD10022764 15604093 details
NRIP1_HUMANVDR_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANHNF4A_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANNR5A2_HUMANBioGRID, HPRD15604093 details
NRIP1_HUMANCDK8_HUMANBioGRID21868449 details
NRIP1_HUMANA4_HUMANBioGRID21832049 details
NRIP1_HUMANBRCA1_HUMANBioGRID25184681 details
NRIP1_HUMANHDAC1_HUMANBioGRID, HPRD11006275 11285237 15060175 details
NRIP1_HUMANHDAC2_HUMANBioGRID, HPRD15060175 details
NRIP1_HUMANAGR2_HUMANBioGRID20888340 details
NRIP1_HUMANNR2C1_HUMANHPRD9774688 details
NRIP1_HUMANTNR14_HUMANHPRD9774688 details
NRIP1_HUMANCARM1_HUMANBioGRID, MINT17053781 details
NRIP1_HUMANXPO2_HUMANMINT17053781 details
NRIP1_HUMANXPO1_HUMANBioGRID17053781 details
NRIP1_HUMANIMB1_HUMANBioGRID17053781 details
NRIP1_HUMANMCR_HUMANBioGRID10935545 details
NRIP1_HUMANPRGC1_HUMANBioGRID19625249 details
NRIP1_HUMANM3K7_HUMANHPRD9556573 details
NRIP1_HUMANKAT2B_HUMANHPRD11509661 14581481 details
NRIP1_HUMANPPARD_HUMANHPRD15001550 details
NRIP1_HUMANANDR_HUMANHPRD9368054 details