Entity Details

Primary name AQP2_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP41181
EntryNameAQP2_HUMAN
FullNameAquaporin-2
TaxID9606
Evidenceevidence at protein level
Length271
SequenceStatuscomplete
DateCreated1995-02-01
DateModified2021-06-02

Ontological Relatives

GenesAQP2

GO terms

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GOName
GO:0003091 renal water homeostasis
GO:0003097 renal water transport
GO:0005372 water transmembrane transporter activity
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0006833 water transport
GO:0015168 glycerol transmembrane transporter activity
GO:0015250 water channel activity
GO:0015793 glycerol transport
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0016324 apical plasma membrane
GO:0030658 transport vesicle membrane
GO:0042631 cellular response to water deprivation
GO:0048471 perinuclear region of cytoplasm
GO:0051289 protein homotetramerization
GO:0055037 recycling endosome
GO:0070062 extracellular exosome
GO:0071280 cellular response to copper ion
GO:0071288 cellular response to mercury ion
GO:0072205 metanephric collecting duct development
GO:0098576 lumenal side of membrane

Subcellular Location

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Subcellular Location
Apical cell membrane
Basolateral cell membrane
Cell membrane
Cytoplasmic vesicle membrane
Golgi apparatus

Domains

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DomainNameCategoryType
IPR000425 Major intrinsic proteinFamilyFamily
IPR022357 Major intrinsic protein, conserved siteSiteConserved site
IPR023271 Aquaporin-likeFamilyHomologous superfamily
IPR034294 Aquaporin transporterFamilyFamily

Diseases

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Disease IDSourceNameDescription
125800 OMIMDiabetes insipidus, nephrogenic, autosomal (ANDI)A disorder caused by the inability of the renal collecting ducts to absorb water in response to arginine vasopressin. Characterized by excessive water drinking (polydipsia), excessive urine excretion (polyuria), persistent hypotonic urine, and hypokalemia. Inheritance can be autosomal dominant or recessive. The disease is caused by variants affecting the gene represented in this entry.

Interactions

67 interactions

InteractorPartnerSourcesPublicationsLink
AQP2_HUMANTMM60_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANPMP22_HUMANIntAct32296183 details
AQP2_HUMANS38A7_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANFAM3C_HUMANIntAct32296183 details
AQP2_HUMANNRM_HUMANIntAct32296183 details
AQP2_HUMANGPX8_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANRTP2_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANEFNA5_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANERMP1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANTM236_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANYIPF6_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANLIPR1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANMUC1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANM4A13_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANOLFM4_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANCDIPT_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANINSI2_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANIBP5_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANTM86A_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANO10AG_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANLEUTX_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANSGMR2_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANMRM1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANF209A_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANERG28_HUMANBioGRID, IntAct28931009 32296183 details
AQP2_HUMANPDZ1I_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANTM218_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANCR3L1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANS26A6_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANTM109_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANPANX1_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANSNP47_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANLHPL5_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANERGI3_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANZNT2_HUMANBioGRID, IntAct32296183 details
AQP2_HUMANCREB3_HUMANBioGRID, IntAct25910212 details
AQP2_HUMANNFIP2_HUMANBioGRID28931009 details
AQP2_HUMANSTX8_HUMANBioGRID28931009 details
AQP2_HUMANIEX1_HUMANBioGRID28931009 details
AQP2_HUMANBAP31_HUMANBioGRID28931009 details
AQP2_HUMANTM230_HUMANBioGRID28931009 details
AQP2_HUMANSPCS1_HUMANBioGRID28931009 details
AQP2_HUMANPLP2_HUMANBioGRID28931009 details
AQP2_HUMANUB2J1_HUMANBioGRID28931009 details
AQP2_HUMANCC167_HUMANBioGRID28931009 details
AQP2_HUMANSSRG_HUMANBioGRID28931009 details
AQP2_HUMANCERT_HUMANBioGRID28931009 details
AQP2_HUMANCLD7_HUMANBioGRID28931009 details
AQP2_HUMANACTB_HUMANBioGRID28931009 details
AQP2_HUMANCD003_HUMANBioGRID28931009 details
AQP2_HUMANEF1A1_HUMANBioGRID28931009 details
AQP2_HUMANSC5A2_HUMANBioGRID28931009 details
AQP2_HUMANSNX5_HUMANBioGRID28931009 details
AQP2_HUMANELL2_HUMANBioGRID28931009 details
AQP2_HUMANVAPB_HUMANBioGRID28931009 details
AQP2_HUMANSP20H_HUMANBioGRID28931009 details
AQP2_HUMANTM9S2_HUMANBioGRID28931009 details
AQP2_HUMANGPAA1_HUMANBioGRID28931009 details
AQP2_HUMANCHIP_HUMANBioGRID29242247 details
AQP2_HUMANCLCA4_HUMANBioGRID32296183 details
AQP2_HUMANPPGB_HUMANBioGRID32296183 details
AQP2_HUMANCXL16_HUMANBioGRID32296183 details
AQP2_HUMANTARG1_HUMANBioGRID32296183 details
AQP2_HUMANNEDD4_HUMANBioGRID28931009 details
AQP2_HUMANHSP7C_HUMANBioGRID29242247 details
AQP2_HUMANHSP74_HUMANBioGRID29242247 details
AQP2_HUMANAQP2_HUMANHPRD11076974 12051765 details