Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
366
Gene name Gene Name - the full gene name approved by the HGNC.
Aquaporin 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AQP9
Synonyms (NCBI Gene) Gene synonyms aliases
AQP-9, HsT17287, SSC1, T17287
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q21.3
Summary Summary of gene provided in NCBI Entrez Gene.
The aquaporins are a family of water-selective membrane channels. This gene encodes a member of a subset of aquaporins called the aquaglyceroporins. This protein allows passage of a broad range of noncharged solutes and also stimulates urea transport and
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT791576 hsa-miR-18a CLIP-seq
MIRT791577 hsa-miR-18b CLIP-seq
MIRT791578 hsa-miR-300 CLIP-seq
MIRT791579 hsa-miR-3136-5p CLIP-seq
MIRT791580 hsa-miR-324-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005275 Function Amine transmembrane transporter activity TAS 9733774
GO:0005345 Function Purine nucleobase transmembrane transporter activity IDA 9733774
GO:0005350 Function Pyrimidine nucleobase transmembrane transporter activity IDA 9733774
GO:0005372 Function Water transmembrane transporter activity TAS 9733774
GO:0005515 Function Protein binding IPI 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602914 643 ENSG00000103569
Protein
UniProt ID O43315
Protein name Aquaporin-9 (AQP-9) (Aquaglyceroporin-9) (Small solute channel 1)
Protein function Aquaglyceroporins form homotetrameric transmembrane channels, with each monomer independently mediating glycerol and water transport across the plasma membrane along their osmotic gradient (PubMed:10564231, PubMed:30420639, PubMed:35054513, PubM
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00230 MIP 17 262 Major intrinsic protein Family
Tissue specificity TISSUE SPECIFICITY: Highly expressed in peripheral leukocytes. Also expressed in liver, lung, and spleen. {ECO:0000269|PubMed:10564231, ECO:0000269|PubMed:9514918}.
Sequence
Sequence length 295
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neutrophil extracellular trap formation
Bile secretion
  Transport of glycerol from adipocytes to the liver by Aquaporins
Passive transport by Aquaporins
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Leukemia leukemia, Leukemia, Myelocytic, Acute, Acute Myeloid Leukemia (AML-M2) rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 15336539, 16968895
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 27026296
Astrocytoma Associate 29485906
Brain Neoplasms Associate 18652774, 24086629
Breast Diseases Associate 33247170
Breast Neoplasms Associate 33247170, 37681917
Carcinoma Hepatocellular Associate 27026296, 36212175
Carcinoma Hepatocellular Inhibit 31969493
Carcinoma Renal Cell Stimulate 31703694, 35245343
Carcinoma Renal Cell Associate 36254092
Crohn Disease Associate 33936061, 36792688, 39475676