AQP1 - aquaporin 1 (Colton blood group) Gene

Also Known as CO; CHIP28; AQP-CHIP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 358

About AQP1

Cytogenetic location: 7p14.3 Genomic coordinates (GRCh38): 7:30,911,853-30,925,516 (from NCBI)

This gene has 8 transcripts (splice variants), 272 orthologues, 11 paralogues and is associated with 1 phenotype. Broad expression in kidney (RPKM 409.8), lung (RPKM 246.0) and 15 other tissues.

Summary

This gene encodes a small integral membrane protein with six bilayer spanning domains that functions as a water channel protein. This protein permits passive transport of water along an osmotic gradient. This gene is a possible candidate for disorders involving imbalance in ocular fluid movement. [provided by RefSeq, Aug 2016]

AQP1 Products (2)

mRNA Protein Name
NM_001329872.2 NP_001316801.1 aquaporin-1 isoform 5
NM_198098.4 NP_932766.1 aquaporin-1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables ammonium channel activity IDA
IDA: Inferred from direct assay
19273840 GOA
enables carbon dioxide transmembrane transporter activity IDA
IDA: Inferred from direct assay
17012249 GOA
enables glycerol transmembrane transporter activity IDA
IDA: Inferred from direct assay
7491270 GOA
enables hydrogen peroxide channel activity IDA
IDA: Inferred from direct assay
33028705 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
17632520 GOA
enables intracellularly cGMP-activated cation channel activity IDA
IDA: Inferred from direct assay
14561230 GOA
enables nitric oxide transmembrane transporter activity IDA
IDA: Inferred from direct assay
16682607 GOA
enables potassium channel activity IMP
IMP: Inferred from mutant phenotype
11914159 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables transmembrane transporter activity IDA
IDA: Inferred from direct assay
17012249 GOA
enables water channel activity EXP
EXP: Inferred from Experiment
1373524 GOA
enables water channel activity IDA
IDA: Inferred from direct assay
9733774 GOA
enables water channel activity IMP
IMP: Inferred from mutant phenotype
19424603 GOA
enables water transmembrane transporter activity IDA
IDA: Inferred from direct assay
7521540 GOA
Biological Process GO Annotation Evidence References Source
involved in ammonium transmembrane transport IDA
IDA: Inferred from direct assay
16574458 GOA
involved in cGMP-mediated signaling IDA
IDA: Inferred from direct assay
14561230 GOA
involved in carbon dioxide transmembrane transport IDA
IDA: Inferred from direct assay
17012249 GOA
involved in carbon dioxide transport IDA
IDA: Inferred from direct assay
12745312 GOA
involved in cell volume homeostasis IMP
IMP: Inferred from mutant phenotype
11922632 GOA
involved in cellular homeostasis IDA
IDA: Inferred from direct assay
19268465 GOA
involved in cellular hyperosmotic response IMP
IMP: Inferred from mutant phenotype
11922632 GOA
involved in cellular response to UV IDA
IDA: Inferred from direct assay
19424603 GOA
involved in cellular response to cAMP IDA
IDA: Inferred from direct assay
18538351 GOA
involved in cellular response to cAMP IEP
IEP: Inferred from expression pattern
17636236 GOA
involved in cellular response to copper ion IDA
IDA: Inferred from direct assay
7491270 GOA
involved in cellular response to dexamethasone stimulus IDA
IDA: Inferred from direct assay
16711029 GOA
involved in cellular response to hydrogen peroxide IDA
IDA: Inferred from direct assay
19424603 GOA
involved in cellular response to hypoxia IDA
IDA: Inferred from direct assay
18275976 GOA
involved in cellular response to mechanical stimulus IDA
IDA: Inferred from direct assay
19268465 GOA
involved in cellular response to mercury ion IDA
IDA: Inferred from direct assay
7491270 GOA
involved in cellular response to nitric oxide IDA
IDA: Inferred from direct assay
14561230 GOA
involved in cellular response to retinoic acid IDA
IDA: Inferred from direct assay
12051745 GOA
involved in cellular response to salt stress IDA
IDA: Inferred from direct assay
18509662 GOA
involved in cerebrospinal fluid secretion IEP
IEP: Inferred from expression pattern
16814974 GOA
involved in defense response to Gram-negative bacterium IMP
IMP: Inferred from mutant phenotype
18665841 GOA
involved in establishment or maintenance of actin cytoskeleton polarity IMP
IMP: Inferred from mutant phenotype
19584911 GOA
involved in glycerol transmembrane transport IDA
IDA: Inferred from direct assay
7491270 GOA
involved in intracellular water homeostasis IDA
IDA: Inferred from direct assay
21251984 GOA
involved in lateral ventricle development IEP
IEP: Inferred from expression pattern
16133142 GOA
involved in multicellular organismal-level water homeostasis IEP
IEP: Inferred from expression pattern
17645239 GOA
involved in negative regulation of apoptotic process IDA
IDA: Inferred from direct assay
16565507 GOA
involved in negative regulation of cysteine-type endopeptidase activity involved in apoptotic process IMP
IMP: Inferred from mutant phenotype
21215257 GOA
involved in nitric oxide transport IDA
IDA: Inferred from direct assay
16682607 GOA
involved in odontogenesis IEP
IEP: Inferred from expression pattern
12522663 GOA
involved in pancreatic juice secretion IEP
IEP: Inferred from expression pattern
12801959 GOA
involved in positive regulation of angiogenesis IMP
IMP: Inferred from mutant phenotype
18275976 GOA
involved in positive regulation of fibroblast proliferation IDA
IDA: Inferred from direct assay
16565507 GOA
involved in positive regulation of saliva secretion IMP
IMP: Inferred from mutant phenotype
9096382 GOA
involved in renal water transport IDA
IDA: Inferred from direct assay
9096382 GOA
involved in transepithelial water transport IDA
IDA: Inferred from direct assay
12766090 GOA
involved in water transport IDA
IDA: Inferred from direct assay
7521540 GOA
involved in water transport IMP
IMP: Inferred from mutant phenotype
19424603 GOA
Cellular Component GO Annotation Evidence References Source
part of ankyrin-1 complex IDA
IDA: Inferred from direct assay
35835865 GOA
located in apical part of cell IDA
IDA: Inferred from direct assay
14675051 GOA
located in apical plasma membrane IDA
IDA: Inferred from direct assay
9013443 GOA
located in basal plasma membrane IDA
IDA: Inferred from direct assay
17409744 GOA
located in basolateral plasma membrane IDA
IDA: Inferred from direct assay
9013443 GOA
located in brush border IDA
IDA: Inferred from direct assay
16133142 GOA
located in brush border membrane IDA
IDA: Inferred from direct assay
9013443 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16814974 GOA
located in extracellular exosome IDA
IDA: Inferred from direct assay
15326289 GOA
located in nuclear membrane IDA
IDA: Inferred from direct assay
17645239 GOA
located in nucleus IDA
IDA: Inferred from direct assay
17645239 GOA
NOT located in plasma membrane IDA
IDA: Inferred from direct assay
7544358 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
7491270 GOA
located in sarcolemma IDA
IDA: Inferred from direct assay
17409744 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

AQP1 Protein Structure

MIP

MIP: Major intrinsic protein (5 - 227)

  • 0
  • 100
  • 200
  • 269 a.a.
Protein Preferred Names Protein Names

aquaporin-1

  • Colton blood group antigen

AQP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
AQP1 P29972 CCDC136 Homo sapiens Q96JN2-2 25416956
Intra
AQP1 P29972 KRT40 Homo sapiens Q6A162 25416956
Intra
AQP1 P29972 KRT40 Homo sapiens Q6A162 25416956
Intra
AQP1 P29972 KRTAP10-8 Homo sapiens P60410 32296183
Intra
AQP1 P29972 KRTAP10-8 Homo sapiens P60410 32296183
Intra
AQP1 P29972 KRTAP10-8 Homo sapiens P60410 32296183
Intra
AQP1 P29972 KRTAP10-7 Homo sapiens P60409 25416956
Intra
AQP1 P29972 KRTAP10-7 Homo sapiens P60409 25416956
Intra
AQP1 P29972 KRTAP10-7 Homo sapiens P60409 25416956
Intra
AQP1 P29972 KRTAP4-2 Homo sapiens Q9BYR5 32296183
Intra
AQP1 P29972 KRTAP4-2 Homo sapiens Q9BYR5 25416956
Intra
AQP1 P29972 KRTAP4-2 Homo sapiens Q9BYR5 32296183
Intra
AQP1 P29972 KRTAP4-2 Homo sapiens Q9BYR5 32296183
Intra
AQP1 P29972 LDLRAD1 Homo sapiens Q5T700 32296183
Intra
AQP1 P29972 LDLRAD1 Homo sapiens Q5T700 32296183
Intra
AQP1 P29972 LDLRAD1 Homo sapiens Q5T700 32296183
Intra
AQP1 P29972 KRTAP12-4 Homo sapiens P60329 32296183
Intra
AQP1 P29972 KRTAP12-4 Homo sapiens P60329 32296183
Intra
AQP1 P29972 KRTAP12-4 Homo sapiens P60329 32296183
Intra
AQP1 P29972 RGS20 Homo sapiens O76081-6 25416956
Intra
AQP1 P29972 KIAA1958 Homo sapiens Q8N8K9 25416956
Intra
AQP1 P29972 KIAA1958 Homo sapiens Q8N8K9 25416956
Intra
AQP1 P29972 RIMBP3 Homo sapiens Q9UFD9 25416956
Intra
AQP1 P29972 FOS Homo sapiens Q6FG41 25416956
Intra
AQP1 P29972 FOS Homo sapiens Q6FG41 25416956
Intra
AQP1 P29972 CRTAC1 Homo sapiens Q9NQ79 25416956
Intra
AQP1 P29972 CRTAC1 Homo sapiens Q9NQ79 25416956
Intra
AQP1 P29972 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
AQP1 P29972 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
AQP1 P29972 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
AQP1 P29972 KRTAP9-2 Homo sapiens Q9BYQ4 25416956
Intra
AQP1 P29972 KRT37 Homo sapiens O76014 32296183
Intra
AQP1 P29972 KRT37 Homo sapiens O76014 32296183
Intra
AQP1 P29972 KRT33B Homo sapiens Q14525 25416956
Intra
AQP1 P29972 RGS20 Homo sapiens O76081 25416956
Intra
AQP1 P29972 RGS20 Homo sapiens O76081 25416956
Intra
AQP1 P29972 TMEM38B Homo sapiens Q9NVV0 32296183
Intra
AQP1 P29972 TMEM38B Homo sapiens Q9NVV0 32296183
Intra
AQP1 P29972 TMEM38B Homo sapiens Q9NVV0 32296183
Intra
AQP1 P29972 REL Homo sapiens Q04864-2 32296183
Intra
AQP1 P29972 REL Homo sapiens Q04864-2 32296183
Intra
AQP1 P29972 REL Homo sapiens Q04864-2 32296183
Intra
AQP1 P29972 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
AQP1 P29972 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
AQP1 P29972 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
AQP1 P29972 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
AQP1 P29972 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
AQP1 P29972 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
AQP1 P29972 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
AQP1 P29972 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
AQP1 P29972 GPRASP3 Homo sapiens Q6PI77 32296183
Intra
AQP1 P29972 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
AQP1 P29972 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
AQP1 P29972 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
AQP1 P29972 GPX8 Homo sapiens Q8TED1 32296183
Intra
AQP1 P29972 GPX8 Homo sapiens Q8TED1 32296183
Intra
AQP1 P29972 GPX8 Homo sapiens Q8TED1 32296183
Intra
AQP1 P29972 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
AQP1 P29972 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
AQP1 P29972 KRTAP1-5 Homo sapiens Q9BYS1 32296183
Intra
AQP1 P29972 TMEM80 Homo sapiens Q96HE8 32296183
Intra
AQP1 P29972 TMEM80 Homo sapiens Q96HE8 32296183
Intra
AQP1 P29972 TMEM80 Homo sapiens Q96HE8 32296183
Intra
AQP1 P29972 CDR2 Homo sapiens Q01850 32296183
Intra
AQP1 P29972 CDR2 Homo sapiens Q01850 32296183
Intra
AQP1 P29972 CDR2 Homo sapiens Q01850 32296183
Intra
AQP1 P29972 KRTAP4-4 Homo sapiens Q9BYR3 32296183
Intra
AQP1 P29972 KRTAP4-4 Homo sapiens Q9BYR3 32296183
Intra
AQP1 P29972 KRTAP4-4 Homo sapiens Q9BYR3 32296183
Intra
AQP1 P29972 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
AQP1 P29972 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
AQP1 P29972 KRTAP9-8 Homo sapiens Q9BYQ0 32296183
Intra
AQP1 P29972 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
AQP1 P29972 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
AQP1 P29972 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
AQP1 P29972 LCE1A Homo sapiens Q5T7P2 32296183
Intra
AQP1 P29972 LCE1A Homo sapiens Q5T7P2 32296183
Intra
AQP1 P29972 LCE1A Homo sapiens Q5T7P2 32296183
Intra
AQP1 P29972 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
AQP1 P29972 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
AQP1 P29972 KRTAP6-2 Homo sapiens Q3LI66 32296183
Intra
AQP1 P29972 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
AQP1 P29972 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
AQP1 P29972 ZIM2 Homo sapiens Q9NZV7 32296183
Intra
AQP1 P29972 RBAK Homo sapiens Q9NYW8 32296183
Intra
AQP1 P29972 RBAK Homo sapiens Q9NYW8 32296183
Intra
AQP1 P29972 RBAK Homo sapiens Q9NYW8 32296183
Intra
AQP1 P29972 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
AQP1 P29972 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
AQP1 P29972 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
AQP1 P29972 ESM1 Homo sapiens Q9NQ30 32296183
Intra
AQP1 P29972 ESM1 Homo sapiens Q9NQ30 32296183
Intra
AQP1 P29972 ESM1 Homo sapiens Q9NQ30 32296183
Intra
AQP1 P29972 SPRY3 Homo sapiens O43610 32296183
Intra
AQP1 P29972 SPRY3 Homo sapiens O43610 32296183
Intra
AQP1 P29972 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
AQP1 P29972 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
AQP1 P29972 SIVA1 Homo sapiens O15304-2 32296183
Intra
AQP1 P29972 SIVA1 Homo sapiens O15304-2 32296183
Intra
AQP1 P29972 SPRYD7 Homo sapiens Q5W111-2 32296183
Intra
AQP1 P29972 SPRYD7 Homo sapiens Q5W111-2 32296183
Intra
AQP1 P29972 SPRYD7 Homo sapiens Q5W111-2 32296183
Intra
AQP1 P29972 IL21R Homo sapiens Q9HBE5 32296183
Intra
AQP1 P29972 IL21R Homo sapiens Q9HBE5 32296183
Intra
AQP1 P29972 IL21R Homo sapiens Q9HBE5 32296183
Intra
AQP1 P29972 SLC15A2 Homo sapiens Q16348 32296183
Intra
AQP1 P29972 SLC15A2 Homo sapiens Q16348 32296183
Intra
AQP1 P29972 SLC15A2 Homo sapiens Q16348 32296183
Intra
AQP1 P29972 TSC1 Homo sapiens Q86WV8 32296183
Intra
AQP1 P29972 TSC1 Homo sapiens Q86WV8 32296183
Intra
AQP1 P29972 TSC1 Homo sapiens Q86WV8 32296183
Intra
AQP1 P29972 PGPEP1 Homo sapiens Q9NXJ5-2 32296183
Intra
AQP1 P29972 PGPEP1 Homo sapiens Q9NXJ5-2 32296183
Intra
AQP1 P29972 PGPEP1 Homo sapiens Q9NXJ5-2 32296183
Intra
AQP1 P29972 SLC39A2 Homo sapiens Q9NP94 32296183
Intra
AQP1 P29972 SLC39A2 Homo sapiens Q9NP94 32296183
Intra
AQP1 P29972 SLC39A2 Homo sapiens Q9NP94 32296183
Intra
AQP1 P29972 AQP6 Homo sapiens Q13520 32296183
Intra
AQP1 P29972 AQP6 Homo sapiens Q13520 32296183
Intra
AQP1 P29972 AQP6 Homo sapiens Q13520 32296183
Intra
AQP1 P29972 MUC1 Homo sapiens P15941-11 32296183
Intra
AQP1 P29972 MUC1 Homo sapiens P15941-11 32296183
Intra
AQP1 P29972 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
AQP1 P29972 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
AQP1 P29972 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
AQP1 P29972 AMOT Homo sapiens A2BDD9 32296183
Intra
AQP1 P29972 AMOT Homo sapiens A2BDD9 32296183
Intra
AQP1 P29972 MYF5 Homo sapiens P13349 32296183
Intra
AQP1 P29972 MYF5 Homo sapiens P13349 32296183
Intra
AQP1 P29972 EVI2B Homo sapiens P34910-2 32296183
Intra
AQP1 P29972 EVI2B Homo sapiens P34910-2 32296183
Intra
AQP1 P29972 EVI2B Homo sapiens P34910-2 32296183
Intra
AQP1 P29972 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
AQP1 P29972 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
AQP1 P29972 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
AQP1 P29972 FAM209A Homo sapiens Q5JX71 32296183
Intra
AQP1 P29972 FAM209A Homo sapiens Q5JX71 32296183
Intra
AQP1 P29972 FAM209A Homo sapiens Q5JX71 32296183
Intra
AQP1 P29972 CLDN5 Homo sapiens O00501 32296183
Intra
AQP1 P29972 CLDN5 Homo sapiens O00501 32296183
Intra
AQP1 P29972 GET1 Homo sapiens O00258 32296183
Intra
AQP1 P29972 GET1 Homo sapiens O00258 32296183
Intra
AQP1 P29972 RNF122 Homo sapiens Q9H9V4 32296183
Intra
AQP1 P29972 RNF122 Homo sapiens Q9H9V4 32296183
Intra
AQP1 P29972 RNF122 Homo sapiens Q9H9V4 32296183
Intra
AQP1 P29972 NOTCH2NLC Homo sapiens P0DPK4 32296183
Intra
AQP1 P29972 NOTCH2NLC Homo sapiens P0DPK4 32296183
Intra
AQP1 P29972 MKRN3 Homo sapiens Q13064 32296183
Intra
AQP1 P29972 MKRN3 Homo sapiens Q13064 32296183
Intra
AQP1 P29972 MKRN3 Homo sapiens Q13064 32296183
Intra
AQP1 P29972 COMP Homo sapiens P49747 32296183
Intra
AQP1 P29972 COMP Homo sapiens P49747 32296183
Intra
AQP1 P29972 COMP Homo sapiens P49747 32296183
Intra
AQP1 P29972 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
AQP1 P29972 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
AQP1 P29972 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
AQP1 P29972 CCDC57 Homo sapiens Q2TAC2 25416956
Intra
AQP1 P29972 TRIM7 Homo sapiens Q9C029 32296183
Intra
AQP1 P29972 TRIM7 Homo sapiens Q9C029 32296183
Intra
AQP1 P29972 TRIM7 Homo sapiens Q9C029 32296183
Intra
AQP1 P29972 LIME1 Homo sapiens Q9H400 32296183
Intra
AQP1 P29972 LIME1 Homo sapiens Q9H400 32296183
Intra
AQP1 P29972 LIME1 Homo sapiens Q9H400 32296183
Intra
AQP1 P29972 GPR37L1 Homo sapiens O60883 32296183
Intra
AQP1 P29972 GPR37L1 Homo sapiens O60883 32296183
Intra
AQP1 P29972 GLI1 Homo sapiens P08151 32296183
Intra
AQP1 P29972 TRAF2 Homo sapiens Q12933 25416956
Intra
AQP1 P29972 LRRC59 Homo sapiens Q96AG4 32296183
Intra
AQP1 P29972 LRRC59 Homo sapiens Q96AG4 32296183
Intra
AQP1 P29972 LRRC59 Homo sapiens Q96AG4 32296183
Intra
AQP1 P29972 TRAF1 Homo sapiens Q13077 25416956
Intra
AQP1 P29972 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
AQP1 P29972 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
AQP1 P29972 IKZF2 Homo sapiens Q9UKS7 25416956
Intra
AQP1 P29972 IKZF2 Homo sapiens Q9UKS7 25416956
Intra
AQP1 P29972 GJB5 Homo sapiens O95377 32296183
Intra
AQP1 P29972 GJB5 Homo sapiens O95377 32296183
Intra
AQP1 P29972 RGS17 Homo sapiens Q9UGC6 25416956
Intra
AQP1 P29972 RGS17 Homo sapiens Q9UGC6 32296183
Intra
AQP1 P29972 RGS17 Homo sapiens Q9UGC6 32296183
Intra
AQP1 P29972 RGS17 Homo sapiens Q9UGC6 25416956
Intra
AQP1 P29972 RGS17 Homo sapiens Q9UGC6 32296183
Intra
AQP1 P29972 BMF Homo sapiens Q96LC9 32296183
Intra
AQP1 P29972 BMF Homo sapiens Q96LC9 32296183
Intra
AQP1 P29972 BMF Homo sapiens Q96LC9 32296183
Intra
AQP1 P29972 SAR1A Homo sapiens Q9NR31 32296183
Intra
AQP1 P29972 SAR1A Homo sapiens Q9NR31 32296183
Intra
AQP1 P29972 SAR1A Homo sapiens Q9NR31 32296183
Intra
AQP1 P29972 ZNF16 Homo sapiens P17020 32296183
Intra
AQP1 P29972 ZNF16 Homo sapiens P17020 32296183
Intra
AQP1 P29972 TMEM45B Homo sapiens Q96B21 32296183
Intra
AQP1 P29972 TMEM45B Homo sapiens Q96B21 32296183
Intra
AQP1 P29972 TMEM45B Homo sapiens Q96B21 32296183
Intra
AQP1 P29972 KCNK5 Homo sapiens O95279 32296183
Intra
AQP1 P29972 KCNK5 Homo sapiens O95279 32296183
Intra
AQP1 P29972 PLSCR2 Homo sapiens Q9NRY7 32296183
Intra
AQP1 P29972 PLSCR2 Homo sapiens Q9NRY7 32296183
Intra
AQP1 P29972 PLSCR2 Homo sapiens Q9NRY7 32296183
Intra
AQP1 P29972 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
AQP1 P29972 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
AQP1 P29972 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
AQP1 P29972 CSRNP1 Homo sapiens Q96S65 25416956
Intra
AQP1 P29972 CSRNP1 Homo sapiens Q96S65 25416956
Intra
AQP1 P29972 SPRED1 Homo sapiens Q7Z699 32296183
Intra
AQP1 P29972 SPRED1 Homo sapiens Q7Z699 32296183
Intra
AQP1 P29972 SPRED1 Homo sapiens Q7Z699 32296183
Intra
AQP1 P29972 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
AQP1 P29972 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
AQP1 P29972 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
AQP1 P29972 TCF4 Homo sapiens P15884 25416956
Intra
AQP1 P29972 TCF4 Homo sapiens P15884 25416956
Intra
AQP1 P29972 TCF4 Homo sapiens P15884 25416956
Intra
AQP1 P29972 MRM1 Homo sapiens Q6IN84 32296183
Intra
AQP1 P29972 MRM1 Homo sapiens Q6IN84 32296183
Intra
AQP1 P29972 MRM1 Homo sapiens Q6IN84 32296183
Intra
AQP1 P29972 FSD2 Homo sapiens A1L4K1 25416956
Intra
AQP1 P29972 FSD2 Homo sapiens A1L4K1 25416956
Intra
AQP1 P29972 GOLGA2 Homo sapiens Q08379 32296183
Intra
AQP1 P29972 GOLGA2 Homo sapiens Q08379 32296183
Intra
AQP1 P29972 GOLGA2 Homo sapiens Q08379 32296183
Intra
AQP1 P29972 CREB3 Homo sapiens O43889-2 25910212
Intra
AQP1 P29972 CREB3 Homo sapiens O43889-2 25910212
Intra
AQP1 P29972 CREB3 Homo sapiens O43889-2 25910212
Intra
AQP1 P29972 SPRED2 Homo sapiens Q7Z698 32296183
Intra
AQP1 P29972 SPRED2 Homo sapiens Q7Z698 32296183
Intra
AQP1 P29972 SPRED2 Homo sapiens Q7Z698 32296183
Intra
AQP1 P29972 SPDYA Homo sapiens Q5MJ70 32296183
Intra
AQP1 P29972 SPDYA Homo sapiens Q5MJ70 32296183
Intra
AQP1 P29972 SPDYA Homo sapiens Q5MJ70 32296183
Intra
AQP1 P29972 FAM161A Homo sapiens Q3B820 32296183
Intra
AQP1 P29972 FAM161A Homo sapiens Q3B820 32296183
Intra
AQP1 P29972 FAM161A Homo sapiens Q3B820 32296183
Intra
AQP1 P29972 KHDRBS3 Homo sapiens O75525 32296183
Intra
AQP1 P29972 KHDRBS3 Homo sapiens O75525 32296183
Intra
AQP1 P29972 MDFI Homo sapiens Q99750 16189514
Intra
AQP1 P29972 MDFI Homo sapiens Q99750 32296183
Intra
AQP1 P29972 MDFI Homo sapiens Q99750 32296183
Intra
AQP1 P29972 MDFI Homo sapiens Q99750 32296183
Intra
AQP1 P29972 MGST3 Homo sapiens O14880 32296183
Intra
AQP1 P29972 MGST3 Homo sapiens O14880 32296183
Intra
AQP1 P29972 KLHL26 Homo sapiens Q53HC5 32296183
Intra
AQP1 P29972 KLHL26 Homo sapiens Q53HC5 32296183
Intra
AQP1 P29972 KLHL26 Homo sapiens Q53HC5 32296183
Intra
AQP1 P29972 TRIM41 Homo sapiens Q8WV44 32296183
Intra
AQP1 P29972 TRIM41 Homo sapiens Q8WV44 32296183
Intra
AQP1 P29972 TRIM41 Homo sapiens Q8WV44 32296183
Intra
AQP1 P29972 PLA2G10 Homo sapiens O15496 32296183
Intra
AQP1 P29972 PLA2G10 Homo sapiens O15496 32296183
Intra
AQP1 P29972 TRIM23 Homo sapiens P36406 32296183
Intra
AQP1 P29972 TRIM23 Homo sapiens P36406 32296183
Intra
AQP1 P29972 TRIM23 Homo sapiens P36406 32296183
Intra
AQP1 P29972 LDOC1 Homo sapiens O95751 32296183
Intra
AQP1 P29972 LDOC1 Homo sapiens O95751 32296183
Intra
AQP1 P29972 TRIM37 Homo sapiens O94972 32296183
Intra
AQP1 P29972 TRIM37 Homo sapiens O94972 32296183
Intra
AQP1 P29972 TRIP6 Homo sapiens Q15654 16189514
Intra
AQP1 P29972 TRIP6 Homo sapiens Q15654 32296183
Intra
AQP1 P29972 TRIP6 Homo sapiens Q15654 25416956
Intra
AQP1 P29972 TRIP6 Homo sapiens Q15654 32296183
Intra
AQP1 P29972 TRIP6 Homo sapiens Q15654 32296183
Intra
AQP1 P29972 SPRY2 Homo sapiens O43597 25416956
Intra
AQP1 P29972 SPRY2 Homo sapiens O43597 25416956
Intra
AQP1 P29972 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
AQP1 P29972 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
AQP1 P29972 BEGAIN Homo sapiens Q9BUH8 32296183
Intra
AQP1 P29972 CEP44 Homo sapiens Q9C0F1 25416956
Intra
AQP1 P29972 LPXN Homo sapiens O60711 32296183
Intra
AQP1 P29972 LPXN Homo sapiens O60711 32296183
Intra
AQP1 P29972 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
AQP1 P29972 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
AQP1 P29972 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
AQP1 P29972 IKZF3 Homo sapiens Q9UKT9 25416956
Intra
AQP1 P29972 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
AQP1 P29972 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
AQP1 P29972 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
AQP1 P29972 CCNDBP1 Homo sapiens O95273 32296183
Intra
AQP1 P29972 CCNDBP1 Homo sapiens O95273 32296183
Intra
AQP1 P29972 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
AQP1 P29972 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
AQP1 P29972 KRTAP3-2 Homo sapiens Q9BYR7 32296183
Intra
AQP1 P29972 CD79A Homo sapiens P11912 32296183
Intra
AQP1 P29972 CD79A Homo sapiens P11912 32296183
Intra
AQP1 P29972 IHO1 Homo sapiens Q8IYA8 25416956
Intra
AQP1 P29972 IHO1 Homo sapiens Q8IYA8 25416956
Intra
AQP1 P29972 ZNF398 Homo sapiens Q8TD17 32296183
Intra
AQP1 P29972 ZNF398 Homo sapiens Q8TD17 32296183
Intra
AQP1 P29972 ZNF398 Homo sapiens Q8TD17 32296183
Intra
AQP1 P29972 IFT20 Homo sapiens Q8IY31-3 32296183
Intra
AQP1 P29972 IFT20 Homo sapiens Q8IY31-3 32296183
Intra
AQP1 P29972 IFT20 Homo sapiens Q8IY31-3 32296183
Intra
AQP1 P29972 MIF4GD Homo sapiens A9UHW6-2 32296183
Intra
AQP1 P29972 MIF4GD Homo sapiens A9UHW6-2 32296183
Intra
AQP1 P29972 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
AQP1 P29972 IGFBP6 Homo sapiens P24592 32296183
Intra
AQP1 P29972 IGFBP6 Homo sapiens P24592 32296183
Intra
AQP1 P29972 KRT31 Homo sapiens Q15323 25416956
Intra
AQP1 P29972 TNS2 Homo sapiens Q63HR2 32296183
Intra
AQP1 P29972 TNS2 Homo sapiens Q63HR2 32296183
Intra
AQP1 P29972 TNS2 Homo sapiens Q63HR2 32296183
Intra
AQP1 P29972 ZBTB39 Homo sapiens O15060 32296183
Intra
AQP1 P29972 ZBTB39 Homo sapiens O15060 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant AQP1 Proteins

Cat. No. Product Name Accession Purity
HY-P72085 AQP1 Protein, Human (His-SUMO) P29972 (G220-K269) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P72086 AQP1 Protein, Human (GST) P29972 (G220-K269) ≥ 90%, as determined by reducing SDS-PAGE.

AQP1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81404 Aquaporin 1 Antibody (YA1149) IHC-P Human
HY-P81404A Aquaporin 1 Antibody (YA1149)(PBS only) IHC-P Human
HY-P86699 Aquaporin 1 Antibody (YA6391) WB, IF-Tissue, IHC-P, IHC-F Human, Mouse, Rat

Related Diseases

Diseases Alias
Blood Group, Colton System
  • Colton Blood Group System

  • CO

  • Aquaporin-1 Deficiency

  • Blood Group System, Colton

Brain Edema
  • Cerebral Edema

  • Intracranial Swelling

  • Wet Brain

Motion Sickness
  • Airsickness

  • Carsickness

  • Seasickness

  • Travel Sickness

  • Riders' Vertigo

Neuromyelitis Optica
  • Devic Disease

  • Devic Syndrome

  • Neuromyelitis Optica Spectrum Disorder

  • Devic'S Disease

  • Devic'S Syndrome

  • Devic'S Neuromyelitis Optica

  • Nmo

  • Nmo Spectrum Disorder

  • Neuromyelitis Optica Spectrum Disorders

  • Devic Neuromyelitis Optica

  • Optic-Spinal Ms

  • Opticospinal Ms

  • Nmosd

  • Opticospinal Multiple Sclerosis

  • Devic

  • Ophthalmoneuromyelitis

  • Optic Neuromyelitis

  • Optic Neuroencephalomyelopathy

  • Nmo - [Neuromyelitis Optica]

  • Optic Neuritis With Demyelination

Chiari Malformation
Nephrogenic Diabetes Insipidus
  • Vasopressin-Resistant Diabetes Insipidus

  • Diabetes Insipidus, Nephrogenic

  • Diabetes Insipidus Nephrogenic

  • Congenital Nephrogenic Diabetes Insipidus

  • Adh Resistant Diabetes Insipidus

  • Diabetes Insipidus Nephrogenic X-Linked

  • Diabetes Insipidus Nephrogenic Type 1

  • Adh-Resistant Diabetes Insipidus

  • Diabetes Insipidus Renalis

  • Ndi

  • Renal Diabetes Insipidus

  • Familial Nephrogenic Diabetes

  • Antidiuretic-Hormone-Resistant Diabetes Insipidus

  • Adiuretin-Resistant Diabetes Insipidus

  • Ndi - [Nephrogenic Diabetes Insipidus]

  • Diabetes Tenuifluus

  • Adh - [Antidiuretic-Hormone] Resistant Diabetes Insipidus

  • Hereditary Nephrogenic Diabetes Insipidus

  • Familial Nephrogenic Diabetes Insipidus

  • Primary Nephrogenic Diabetes Insipidus

Oligohydramnios
  • Oligohydramnios - Delivered

  • Antepartum Oligohydramnios

  • Delivered Oligohydramnios

  • Oligohydramnios, Antepartum Condition Or Complication

  • Deficient Liquor

  • Oligohydramnios, Unspecified Trimester

  • Reduced Liquor Volume

Priapism
  • Mentulagra

  • Priapism, Familial Idiopathic

  • Familial Idiopathic Priapism

  • Pathologic Erection

  • Painful Erection

Peritonitis
  • Retractile Mesenteritis

  • Sclerosing Mesenteritis

  • Acute Generalized Peritonitis

  • Primary Bacterial Peritonitis

  • Idiopathic Sclerosing Mesenteritis

  • Mesenteric Panniculitis

  • Peritoneal Retractile Mesenteritis

  • Liposclerotic Mesenteritis

  • Mesenteric Fibromatosis

  • Mesenteric Lipodystrophy

  • Mesenteric Lipogranuloma

  • Fibromatosis, Abdominal

  • Peritoneum Inflammation

  • Peritonitis Of Undetermined Cause

  • Peritonitis Of Unspecified Cause

  • Pelviperitonitis

  • Pelvic Peritonitis, Nos

  • Generalised Peritonitis Nos

  • Abdominal Peritonitis

  • Acute Idiopathic Peritonitis

  • Acute Lesser Sac Peritonitis

  • Acute Peritoneal Inflammation

  • Diffuse Peritonitis

  • Peritoneal Inflammation

  • Acute Primary Peritonitis

  • Pneumococcal Peritonitis

Hydrarthrosis
Intracranial Hypertension, Idiopathic
  • Pseudotumor Cerebri

  • Idiopathic Intracranial Hypertension

  • Benign Intracranial Hypertension

  • Iih

  • Benign Intracran. Hypt.

Fuchs' Endothelial Dystrophy
  • Fuchs Endothelial Corneal Dystrophy

  • Fuchs Endothelial Dystrophy

  • Fuchs Dystrophy

  • Fced

  • Fuchs' Corneal Dystrophy

  • Fuchs' Endothelial Corneal Dystrophy

  • Fuchs Atrophy

  • Fuchs Corneal Dystrophy

  • Endoepithelial Corneal Dystrophy

  • Fecd

  • Late Hereditary Endothelial Dystrophy

  • Corneal Dystrophy, Fuchs Endothelial

  • Dystrophy, Corneal, Fuchs Endothelial

  • Corneal Dystrophy, Fuchs' Endothelial, 1

Hepatorenal Syndrome
  • Hepato-Renal Syndrome

  • Hepatorenal Failure

  • Hrf - [Hepatorenal Failure]

  • Hepatorenal Degeneration

  • Hepatic Renal Syndrome

  • Hepatic Renal Failure

  • Renal Hepatic Failure

  • Urohepatic Syndrome

Hydrocephalus
  • Hydrocephalus, Nonsyndromic, Autosomal Recessive

  • Hydrocephalus, X-Linked

  • Hydrocephalus Adverse Event

  • Hydrocephaly Nos

Corneal Endothelial Dystrophy
  • Congenital Hereditary Endothelial Dystrophy Of Cornea

  • Chandler Syndrome

  • CHED

  • Chandler'S Syndrome

  • Endothelial Corneal Dystrophy

  • Ched2

  • Maumenee Corneal Dystrophy

  • Corneal Dystrophy, Congenital Hereditary Endothelial

  • Dystrophy Of Corneal Endothelium

  • Corneal Endothelial Dystrophy 2

  • Corneal Endothelial Dystrophy 2, Autosomal Recessive, Formerly

  • Ched2, Formerly

  • Corneal Endothelial Dystrophy, Autosomal Recessive

  • Endothelial Dystrophy

  • Posterior Membrane Corneal Dystrophy

  • Corneal Endothelial Dystrophy Type 2

  • Congenital Hereditary Endothelial Dystrophy Of The Cornea

  • Congenital Hereditary Endothelial Dystrophy Type Ii

  • Autosomal Recessive Ched

  • Autosomal Recessive Congenital Hereditary Endothelial Dystrophy

  • Chedii

  • Congenital Hereditary Endothelial Dystrophy Type 2

  • Infantile Hereditary Endothelial Dystrophy

  • Congenital Hereditary Endothelial Corneal Dystrophy

  • Corneal Endothelial Dystrophy 2, Autosomal Recessive

  • Iridocorneal Endothelial Syndrome

  • Dystrophy, Corneal, Endothelial

  • Corneal Endothelial Dystrophy 1, Autosomal Dominant

Leptospirosis
  • Fort Bragg Fever

  • Weil Disease

  • Leptospirosis Icterohaemorrhagica

  • Nanukayami Fever

  • Canicola Fever

  • Hemorrhagic Jaundice

  • Mud Fever

  • Stuttgart Disease

  • Swamp Fever

  • Rat Catcher'S Yellows

  • Spirochetal Jaundice

  • Weil'S Disease

  • Cane-Cutter Fever

  • Icterohemorrhagic Fever

  • Rice-Field Fever

  • Swineherd'S Disease

  • Weil Syndrome

  • Nanukayami

  • Canine Leptospirosis

  • Equine Infectious Anemia

  • Leptospirosis Canicola

  • Fever Due To Leptospira Autumnalis

  • Gikiyami

  • Leptospira Interrogans Autumnalis Infection

  • Leptospira Interrogans Canicola Infection

  • Leptospira Interrogans Hebdomadis Infection

  • Leptospira Interrogans Pomona Infection

  • Nanukayami Disease

  • Pretibial Fever

  • Seven-Day Fever

  • Eia - [Equine Infectious Anaemia]

  • Leptospira Interrogans Infection

Gestational Diabetes Insipidus
  • Transient Diabetes Insipidus Of Pregnancy

  • Diabetes Insipidus Gestational

  • Gestagenic Diabetes Insipidus

  • Doid:0081057

Obstructive Hydrocephalus
X-Linked Nephrogenic Diabetes Insipidus
  • Nephrogenic Diabetes Insipidus Type 1

  • Doid:0081060

Neuroma
Inner Ear Disease
  • Labyrinthine Dysfunction

  • Diseases Of Inner Ear

  • Labyrinthine Disease

  • Abnormality Of The Inner Ear

  • Labyrinth Diseases

  • Labyrinthine Disorder

  • Nonfunctioning Labyrinth

  • Labyrinthine Loss Of Function

  • Labyrinthine Syndrome

  • Labyrinthine Disorder Nos

Oncocytoma
  • Oxyphilic Adenoma

  • Follicular Adenoma, Oxyphilic Cell

  • Adenoma, Oxyphilic

  • Hurthle Cell Tumor

  • Oncocytic Neoplasm

Polyhydramnios
Kidney Cancer
  • Renal Cancer

  • Renal Carcinoma

  • Kidney Neoplasm

  • Malignant Neoplasm Of Kidney Except Pelvis

  • Malignant Tumour Of Kidney

  • Kidney Neoplasms

  • Cancer, Kidney

  • Cancer, Renal

  • Malignant Neoplasm Of Kidney

  • Renal Cell Carcinoma

Pulmonary Hypertension
  • Primary Pulmonary Hypertension

  • Hypertension Pulmonary

  • Hypertension, Pulmonary

  • Hypertension, Pulmonary, Primary

  • Idiopathic Pulmonary Hypertension

  • Idiopathic Pulmonary Arterial Hypertension

  • Pulmonary Htn - [Hypertension]

Intraocular Pressure Quantitative Trait Locus
  • Glaucoma

  • IOPQTL

  • Glaucoma, Susceptibility To

  • Postinfectious Glaucoma

  • Glaucoma With Ocular Inflammation

  • Glaucoma Secondary To Eye Inflammation

  • Traumatic Glaucoma

  • Glaucoma With Concussion Of Globe

  • Glaucoma Due To Ocular Trauma

  • Glaucoma Associated With Ocular Trauma

  • Glaucoma Secondary To Drugs

Communicating Hydrocephalus
  • Acquired Communicating Hydrocephalus

Hypomagnesemia 2, Renal
  • Renal Hypomagnesemia 2

  • HOMG2

  • Magnesium Wasting, Renal

  • Autosomal Dominant Primary Hypomagnesemia With Hypocalciuria

  • Magnesium Loss, Isolated Renal

  • Isolated Autosomal Dominant Hypomagnesemia

  • Isolated Renal Magnesium Wasting

  • Renal Hypomagnesemia Type 2

  • Hypomagnesemia 2

  • Dominant Renal Hypomagnesemia

  • Hypomagnesemia With Hypocalciuria

  • Isolated Renal Magnesium Loss

  • Renal Magnesium Wasting

  • Hypomagnesemia-2, Renal

  • Renal Hypomagnesemia, Dominant

  • Hypomagnesemia, Type 2, Renal

Central Pontine Myelinolysis
  • Myelinolysis, Central Pontine

  • Osmotic Demyelination Syndrome

  • Cpm

  • Myelinolysis Central Pontine

  • Central Pontine Myelinosis

Peripheral Vertigo
  • Vertigo, Peripheral

Cerebrovascular Benign Neoplasm
Autoimmune Disease Of Peripheral Nervous System
Breast Adenoma
  • Ademoma - Breast

Corneal Edema
  • Corneal Oedema

  • Infiltrate Of Cornea

Papilloma Of Choroid Plexus
  • Choroid Plexus Papilloma

  • CPP

  • Childhood Choroid Plexus Papilloma

  • Papilloma Choroid Plexus

  • Papilloma, Choroid Plexus

  • Choroid Plexus Carcinoma

Pulmonary Venoocclusive Disease
  • Pulmonary Veno-Occlusive Disease

  • Obstructive Disease Of The Pulmonary Veins

  • Pvod

  • Isolated Pulmonary Venous Sclerosis

  • Venous Form Of Primary Pulmonary Hypertension

  • Pulmonary Venoocclusive Disease 1, Autosomal Dominant

Intracranial Hypertension
  • Raised Intracranial Pressure

Normal Pressure Hydrocephalus
  • Low Pressure Hydrocephalus

  • Hydrocephalus Normal Pressure

  • Hydrocephalus, Normal Pressure

  • Normal Pressure Hydrocephalus Nos

  • Nph - [Normal Pressure Hydrocephalus]

  • Normal Pressure Hydrocephaly

Urinary Tract Obstruction
  • Obstructive Uropathy

  • Urinary Obstruction

  • Urologic Diseases

Cataract
  • Cataracts

  • Cat - [Cataract]

  • Cataract Form

  • Lens Opacity

  • Lens Opacities

Anemia, Congenital Dyserythropoietic, Type Ib
  • CDAN1B

  • Congenital Dyserythropoietic Anemia Type Ib

  • Cda, Type Ib

  • Congenital Dyserythropoietic Anemia Type Type 1b

  • Dyserythropoietic Anemia, Congenital, Type Ib

  • Anemia, Congenital Dyserythropoietic, 1b

  • Cda Ib

  • Anemia, Dyserythropoietic, Congenital

  • Anemia, Dyserythropoietic, Congenital, Type Ib

Malaria
  • Malaria, Susceptibility To

  • Malaria, Resistance To

  • Malaria, Cerebral

  • Cerebral Malaria

  • Malaria, Severe, Susceptibility To

  • Malaria, Severe, Resistance To

  • Malaria, Cerebral, Susceptibility To

  • Induced Malaria

  • Malaria, Vivax, Protection Against

  • Malaria, Severe

  • Malaria, Cerebral, Reduced Risk Of

  • Malaria, Protection Against

  • Resistance To Malaria Due To G6pd Deficiency

  • Malaria Due To G6pd Deficiency

  • Malarial Encephalitis

  • CM

  • Malaria Cerebral

  • Susceptibility To Malaria

  • Acute Pernicious Fever

  • Aestivo-Autumnal Fever

  • Aestivo Autumnal Malaria

  • Chagres Fever

  • Continued Malaria Fever

  • Estivo-Autumnal Fever

  • Estivo-Autumnal Malaria

  • Estivo-Autumnal Malarial Fever

  • Falciparum Fever

  • Malignant Tertian Fever

  • Malignant Tertian Malaria

  • Pernicious Intermittent Fever

  • Pernicious Malaria

  • Quotidian Malaria

  • Subtertian Fever

  • Subtertian Malaria Fever

  • Subtertian Malignant Tertian Malaria

  • Tropical Malaria

  • Algid Malaria

  • Bilious Haemoglobinuric Fever

  • Black Water Fever

  • Blackwater Fever

  • Malarial Blackwater Fever

  • Severe Malarial Falciparum

  • West African Fever

  • Malarial Haematinuria

  • Haemoglobinuric Fever

  • Haemoglobinuric Malaria

  • Severe Plasmodium Falciparum Malaria

  • Malarial Haemoglobinuria

  • Malarial Haematuria

  • Falciparum Malaria [Malignant Tertian]

  • Malaria Tropica

  • Malarial Shock

  • Chagres Virus Disease

  • Malignant Malaria

  • Mtm - [Malignant Tertian Malaria]

  • Tm -[Malignant Tertian Malaria]

  • Panama Fever

  • St - [Subtertian Malaria]

  • Malarial Quotidian

  • Benign Tertian Malaria

  • Tertian Ague

  • Vivax Fever

  • Plasmodium Vivax Malaria Nos

  • Btm - [Benign Tertian Malaria]

  • Bt - [Benign Tertian Malaria]

  • Vivax Malaria

  • Benign Tertian Vivax Malaria

  • Tertian Malaria

  • Quartan Malaria

  • Quartan Ague

  • Quartan Fever

  • Plasmodium Malariae Malaria Nos

  • Quartan Malarial

  • Malaria By Plasmodium Malariae

  • Malariae Malaria

  • Ovale Tertian Malaria

  • Plasmodium Ovale Fever

  • Malaria Fever By Plasmodium Ovale

  • Ovale Malaria

  • Malaria By Plasmodium Ovale

  • Malarial Ovale

  • Marsh Fever

  • Remittent Congestive Fever

  • Coastal Fever

  • Remittent Gastric Fever

  • Miasmatic Fever

  • Congestive Remittent Fever

  • Intermittent Fever

  • Jungle Fever

  • Paludism

  • Cameroon Fever

  • Ague

  • Corsican Fever

  • Intermittent Bilious Fever

  • Disease Due To Plasmodiidae

  • Malarial Fever

  • Plasmodiosis

  • Remittent Fever

  • Roman Fever

  • Malaria Fever Nos

  • Malaria Nos

  • Paludal Fever

  • Clinically Diagnosed Malaria

  • Clinically Diagnosed Malaria Without Parasitological Confirmation

  • Congestive Fever

  • Malarial Cachexia

  • Marsh Cachexia

  • Paludal Cachexia

  • Recurrent Malaria

  • Remittent Malaria

Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease
  • Polycystic Kidney Disease 1

  • PKD1

  • Adpkd

  • Polycystic Kidney Disease, Adult, Type I

  • Apkd1

  • Potter Type Iii Polycystic Kidney Disease

  • Polycystic Kidney Disease, Adult

  • Potter Type Iii Polycystic Kidney Disease, Formerly

  • Polycystic Kidney Disease, Type 1

  • Adpkd1

  • Adult Polycystic Kidney Disease Type 1

  • Autosomal Dominant Polycystic Kidney Disease 1

  • Pkd-1

  • Polycystic Kidney Disease Adult

  • Polycystic Kidney Disease Type I

  • Polycystic Kidneys

  • Polycystic Kidney Disease, Adult Type I

  • Polycystic Kidney Type 1 Autosomal Dominant Disease

  • Kidney Disease, Polycystic, Type 1

  • Polycystic Kidney, Autosomal Dominant

  • Polycystic Kidney, Type 1 Autosomal Dominant Disease

  • Polycystic Kidney Diseases

Cerebral Degeneration
  • Brain Degeneration

  • Degenerative Brain Disorder

Hereditary Spherocytosis
  • Congenital Spherocytic Hemolytic Anemia

  • Spherocytic Anemia

  • Congenital Spherocytosis

  • Spherocytosis, Type 1

  • Minkowski Chauffard Syndrome

  • Hs

  • Minkowski-Chauffard Disease

  • Minkowski-Chauffard Syndrome

  • Spherocytosis Hereditary

  • Spherocytosis, Hereditary

  • Anemia, Hereditary Spherocytic Hemolytic

Autosomal Dominant Polycystic Kidney Disease
  • Polycystic Kidney Disease, Adult Type

  • Adpkd

  • Polycystic Kidney Diseases

  • Polycystic Kidney, Autosomal Dominant

  • Congenital Biliary Ectasias

  • Polycystic Kidney And Hepatic Disease 1

  • Polycystic Kidney Disease, Autosomal Dominant

  • Kidney, Polycystic, Disease, Autosomal Dominant

  • Adult Polycystic Kidney Disease

  • Polycystic Kidney, Adult Type

  • Apckd - [Autosomal Polycystic Kidney Disease]

Polycystic Liver Disease
  • Autosomal Dominant Polycystic Liver Disease

  • Isolated Polycystic Liver Disease

  • Pcld

  • Congenital Cystic Liver Disease

  • Congenital Hepatic Cyst

  • Fibrocystic Liver Disease

  • Isolated Autosomal Dominant Polycystic Liver Disease

  • Adpcld

  • Liver Disease, Polycystic

  • Multiple Cysts Of Liver

  • Pld - [Polycystic Liver Disease]

  • Polycystic Liver Disorder

  • Polycystic Liver

  • Congenital Polycystic Disease Of Liver

  • Congenital Polycystic Liver Disease

Optic Nerve Disease
  • Optic Neuropathy

  • Disorder Of The Second Nerve

  • Optic Nerve Disorder

  • Optic Nerve

  • Abnormality Of The Optic Nerve

  • Optic Nerve Disorders

  • Neuropathy, Optic

  • Disorder Of The Optic Nerve

Glaucoma, Primary Open Angle
  • Glaucoma 1, Open Angle, E

  • Primary Open Angle Glaucoma

  • POAG

  • Adult-Onset Primary Open Angle Glaucoma

  • Chronic Simple Glaucoma

  • GLC1E

  • Primary Open Angle Glaucoma 1e

  • Glaucoma, Open Angle, Primary

Renal Cell Carcinoma, Nonpapillary
  • Renal Cell Carcinoma

  • RCC

  • Nonpapillary Renal Cell Carcinoma

  • Clear Cell Renal Cell Carcinoma

  • Hypernephroma

  • Adenocarcinoma Of Kidney

  • Renal Carcinoma, Chromophobe, Somatic

  • Clear Cell Carcinoma Of Kidney

  • Clear-Cell Metastatic Renal Cell Carcinoma

  • Clear Cell Renal Carcinoma

  • Renal Cell Carcinoma, Somatic

  • Conventional Renal Cell Carcinoma

  • Conventional Renal Cell Carcinoma

  • Renal Clear Cell Carcinoma

  • Ccrcc

  • Hereditary Clear Cell Renal Cell Carcinoma

  • Carcinoma, Renal Cell

  • Renal Cell Carcinoma, Clear Cell, Somatic

  • Renal Cell Carcinoma, Clear Cell

  • Clear Cell Kidney Carcinoma

  • Clear Cell Rcc

  • Cystic-Multilocular Variant

  • Clear Cell Renal Cell Adenocarcinoma

  • Hereditary Clear Cell Renal Cell Adenocarcinoma

  • Common Renal Cell Carcinoma

  • Crcc

  • Renal Cell Carcinoma Non-Papillary

  • Carcinoma Renal Cell

  • Renal Cell Cancer

  • Carcinoma, Renal Cell, Nonpapillary

Joubert Syndrome 1
  • Joubert Syndrome

  • Jbts

  • Cerebellooculorenal Syndrome 1

  • JBTS1

  • Joubert-Boltshauser Syndrome

  • Cerebelloparenchymal Disorder Iv

  • Cpd4

  • Cors1

  • Joubert Syndrome And Related Disorders

  • Jsrd

  • Familial Aplasia Of The Vermis

  • Joubert Syndrome Related Disorders

  • Js

  • Cerebellar Vermis Agenesis

  • Cerebelloparenchymal Disorder 4

  • Agenesis Of Cerebellar Vermis

  • Cerebello-Oculo-Renal Syndrome

  • Cors

  • Joubert-Bolthauser Syndrome

  • Cpd Iv

  • Classic Joubert Syndrome

  • Joubert Syndrome Type A

  • Pure Joubert Syndrome

  • Cerebello-Oculo-Renal Syndrome 1

  • Joubert Syndrome-1

  • Joubert Syndrome, Type 1

  • Joubert'S Syndrome

Polycystic Kidney Disease
  • Polycystic Kidney Diseases

  • Pkd

  • Polycystic Renal Disease

  • Kidney Disease, Polycystic

  • Polycystic Kidney, Autosomal Dominant

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus AQP1 RGD RGD:2141
Bos taurus AQP1 VGNC VGNC:107216
Macaca mulatta AQP1 VGNC VGNC:81286
Mus musculus AQP1 MGD MGI:103201
Others AQP1 NCBI